US Market News
4日前
MindWalk's Preclinical Dengue Data Support a HYFT® Computational Prediction: Immunogens Designed on the Predicted Target Elicited Cross-Reactive Antibodies Against Antigens of All Four Dengue Serotypes, Reproduced Across Two Independent CampaignsJune 2, 2026 7:20 AM
Business Wire HYFT® technology computationally identified and prioritized a pan-serotype dengue target before immunization. Preclinical data support the prediction at the binding level: immunization with immunogens designed on the predicted target elicited antibodies that cross-react with antigens of all four dengue serotypes, and scrambled-sequence controls support that the response is specific to the designed immunogen rather than background reactivity. MindWalk Holdings Corp. (Nasdaq: HYFT) today reported preclinical dengue data that support a computational prediction its HYFT® platform generated before any animal was immunized. HYFT® computationally identified a candidate pan-serotype structural target on the dengue virus. The subsequent immunization data support that prediction at the antibody-binding level: animals immunized with immunogens designed on the predicted target generated antibodies that cross-reacted with antigens of all four dengue serotypes — a clear and consistent trend, reproduced at the cohort level across two independent campaigns that used distinct immunogen formats and adjuvants. Scrambled-sequence controls did not show the same cross-serotype recognition, indicating the response was specific to the designed immunogen. The result carries implications beyond the dengue program. AI-driven drug discovery depends on biological ground truth — experimentally grounded signal connecting a computational prediction to a measurable outcome in living systems. That substrate has been largely absent from the field: generated inconsistently, outside regulated frameworks, and rarely structured to meet the demands of enterprise AI deployment. The HYFT® platform is designed to produce it. Today's data are MindWalk's first public evidence that it can. Today's data document the platform delivering on its fundamental claim: HYFT® technology computationally prioritized the pan-serotype target before immunization, the experiment supported the binding-level prediction, and the experimentally supported target now anchors MindWalk's dengue pipeline IP position as a persistent asset within the company's Biointelligence Platform. The same predictive capability applied in dengue is being deployed across MindWalk's influenza program and other announced programs where multi-strain coverage presents the analogous design challenge. "The central question for any AI drug discovery platform is whether its computational predictions correspond to real biology," said Dr. Jennifer Bath, PhD, Chief Executive Officer and President of MindWalk Holdings Corp. "HYFT® is built to identify functional patterns that are constrained by biophysical reality — patterns that evolution cannot easily escape because they are tied to structural and binding requirements. We identified the dengue target region not because it appeared conserved at the sequence level, but because HYFT® recognized it as functionally constrained in a way that conventional sequence analysis would not prioritize. “When animals immunized with immunogens built around that prediction produced antibodies that recognized antigens from all four dengue serotypes — and scrambled-sequence controls did not — the prediction was supported in a live immunological system. That is a closed prediction-to-result loop, and it is the first time we have documented one on this vaccine platform. The antibodies’ functional profile — whether they neutralize virus and how they interact with ADE pathways — is what the next body of work will determine. What the current result tells us is that the platform identified real biology. The question now is how broadly that capability holds.” The Market: An Unsolved Pan-Serotype Problem in a High-Burden Infectious Disease Dengue infects an estimated 400 million people annually across four antigenically distinct serotypes. Approved dengue vaccines reach only previously seropositive populations because cross-reactive antibodies against one serotype can enhance, rather than neutralize, disease upon first exposure to a second — antibody-dependent enhancement (ADE). The unsolved pan-serotype problem has kept a significant portion of the endemic seronegative population outside the addressable market for dengue vaccination, and has made a validated pan-serotype immunogen IP position the critical upstream asset for every next-generation dengue vaccine, broad dengue antibody, and pan-flaviviral platform program in development. Identifying that position requires operating below the level of sequence homology. Serotype-to-serotype sequence identity across dengue envelope domain III (EDIII) ranges from 74 to 83 percent — high enough to generate broadly cross-reactive antibodies, insufficient to distinguish a functionally constrained pan-serotype target from a cross-reactive decoy. HYFT® is designed to make that distinction. Rather than relying on sequence alignment or predicted immunogenicity — the parameters conventional target selection leans on — HYFT® identifies functional patterns shaped by biophysical constraints: structure, charge distribution, and binding geometry that remain conserved despite evolutionary diversification because biology cannot easily abandon them. Within MindWalk's Biointelligence Platform, these HYFT® patterns function as biological anchor points that connect sequence information to structural context, literature-supported biology, and experimental evidence. That connection is made through LensAI™, MindWalk's contextualization and reasoning layer, and the Company's Knowledge Graph — a persistent biological intelligence layer that accumulates and links evidence across programs. The significance of the current dengue data is therefore broader than a single dengue vaccine-design experiment: it provides initial experimental evidence for a repeatable discovery loop in which computationally prioritized biological patterns are tested in vivo, and the resulting evidence can be reused across future discovery programs. The current data support cross-serotype antibody recognition at the binding level; future studies will determine whether these antibodies neutralize virus and assess their relationship to antibody-dependent enhancement. “Animals immunized with the immunogens we designed around the HYFT®-identified target generated antibody responses that recognized antigens from all four dengue serotypes, while scrambled-control immunizations did not show the same cross-serotype recognition profile,” said Dirk Van Hyfte, MD, PhD, Chief Technology Officer of MindWalk Holdings Corp. "HYFT® computationally prioritized the target region before immunization, and the subsequent antibody-binding data are consistent with that prediction. For MindWalk, the important result is not only the observed binding response, but also the demonstration that computational biological anchors can be connected to structural analysis, immunogen design, experimental readouts, and a reusable evidence layer." Platform Implications MindWalk's Biointelligence Platform is built around three complementary components. HYFT® identifies biologically meaningful anchor patterns across sequence and structural space. The Knowledge Graph connects those patterns to structural, functional, literature, and experimental evidence. LensAI™ provides the contextualization and reasoning layer that enables scientists and AI models to operate over a common biological representation. Together, these components are designed to create a reusable biological intelligence infrastructure rather than a workflow optimized for any single disease program. MindWalk's Knowledge Graph currently contains hundreds of millions of biological patterns and tens of billions of biological relationships accumulated through years of biological data integration and enrichment. Each experimentally supported result contributes additional evidence to this growing representation, strengthening its potential value across future programs in infectious disease, immunology, protein engineering, and therapeutic discovery. The dengue study also demonstrates the platform's ability to identify both broadly conserved and biologically differentiated patterns within the same analytical framework — a capability particularly relevant to discovery programs where balancing broad coverage and selective targeting represents a central design challenge. About MindWalk Holdings Corp. MindWalk Holdings Corp. (NASDAQ: HYFT) is a bio-native AI company building the biological intelligence infrastructure that life sciences AI and agentic AI require. Its proprietary HYFT system functions as the AI-ready data substrate for life sciences -- a function-aware representation organized around HYFT pattern-objects that span sequence and structural biology, refined over 15 years of curation by a continuously evolving Knowledge Graph of 660 million biological patterns and 25 billion relationships, that enriches data at ingestion and compounds in analytical value with every program run on the platform. The LensAI platform operates on this infrastructure to enable target discovery, candidate diligence, and portfolio decision support, and to host the agentic AI workflows pharma is racing to deploy. MindWalk’s architecture is designed so that the HYFT representation layer -- not any individual AI model -- is the durable, compounding competitive asset. The Company operates antibody discovery sites in Victoria, British Columbia and Fargo, North Dakota. Forward-Looking Statements This press release contains forward-looking statements within the meaning of applicable United States and Canadian securities laws. Forward-looking statements are often identified by terms such as “expects,” “intends,” “plans,” “anticipates,” “believes,” “estimates,” “targets,” or similar expressions, or by statements that certain actions, events, or results are expected to occur or be achieved. Forwardlooking statements in this press release include, without limitation, statements regarding: the current status and anticipated advancement of the Company’s wholly owned pan-serotype Dengue program, which is at the preclinical, in vivo proof-of-concept stage; the anticipated characterization of whether the cross-reactive binding antibodies described in this release neutralize virus and of their relationship to antibody-dependent enhancement (ADE), as to which no results have been disclosed; the interpretation of the preclinical binding data as supporting a computational prediction generated by the HYFT® platform before immunization; the characterization of HYFT® pattern-objects and the LensAI™ platform as capable of identifying functionally constrained biological targets and of supporting a repeatable discovery loop whose resulting evidence can be reused across future programs; the characterization of the experimentally supported dengue target as a persistent asset within the Company’s Biointelligence Platform and The Knowledge Graph; the application of the same predictive capability across the MindWalk Holdings Corp. | Nasdaq: HYFT | Page 4 Company’s influenza program and other announced programs where multi-strain or multi-serotype coverage presents an analogous design challenge; the characterization of The Knowledge Graph’s scale (660 million biological patterns and 25 billion relationships); the anticipated provision of pipeline updates as milestones are reached; and statements regarding the structural, functional, or competitive characteristics of the HYFT® biological pattern system and the LensAI™ platform. Cross-reactive antibody binding observed in preclinical studies does not ensure that such antibodies will neutralize virus, will avoid antibody-dependent enhancement, or will translate into clinical advancement or commercial success of any program. Forward-looking statements are based on management’s current expectations and assumptions and are subject to known and unknown risks, uncertainties, and other factors that may cause actual results to differ materially, including: risks relating to the outcome of ongoing and future in vivo studies, neutralization assays, and ADE characterization; the ability to advance programs from proof-of-concept to clinical development; regulatory determinations; competition; intellectual property risks; the technical performance of AI-based discovery methods; the ability to enter into pharmaceutical or other partnership arrangements; and capital markets conditions. Additional information is available in MindWalk’s Annual Report on Form 20-F and other filings on SEDAR+ (sedarplus.ca) and EDGAR (sec.gov/edgar). Except as required by law, MindWalk undertakes no obligation to update any forwardlooking statement. Nothing in this press release constitutes investment advice. This press release does not constitute an offer to sell or the solicitation of an offer to buy any securities. Trademarks HYFT®, LensAI™, HYFT Base™, HYFT Matrix™, HYFT Prime™, and B cell Llama™ are trademarks of MindWalk Holdings Corp. or its subsidiaries. All other trademarks are the property of their respective owners. Source: MindWalk Holdings Corp. View source version on businesswire.com: https://www.businesswire.com/news/home/20260602948506/en/ Investor Contact
Louie Toma, CPA, CFA
Managing Director, CoreIR
investors@mindwalkai.com Original: MindWalk's Preclinical Dengue Data Support a HYFT® Computational Prediction: Immunogens Designed on the Predicted Target Elicited Cross-Reactive Antibodies Against Antigens of All Four Dengue Serotypes, Reproduced Across Two Independent Campaigns
US Market News
3週前
The Biology Came First.May 18, 2026 8:34 AM
Business Wire Over 20 partner-owned drug programs have reached clinical trials as a result of antibody discovery work performed by MindWalk scientists — ten currently in active Phase 1–3. The same scientific depth and biological intelligence infrastructure behind that record drives the Company's work today. MindWalk Holdings Corp. (NASDAQ: HYFT) today released a systematic report identifying over 20 discovery-originated drug candidates with documented origins in antibody discovery work performed at MindWalk facilities. Ten of these programs are in active clinical trials, spanning Phase 1 through Phase 3 across oncology, immunology, neurology, and infectious disease. In every case, the clinical asset is wholly owned, advanced, and funded by the partner. MindWalk’s contribution was the molecule itself — the immunization strategy, the discovery campaign, the lead identification, and the candidate selection that made clinical entry possible. In select cases that contribution extended into early development. The same wet-lab and AI capabilities that produced these programs are available to MindWalk’s partners today and are the foundation of the Company’s own proprietary portfolio. The full report, available Here, identifies each partner by program. The significance of this record extends beyond the clinical count. The more than 400 peer-reviewed publications and patents produced through this work establish a scientific standard that is rare in this industry: a discovery capability that has consistently produced partner-owned clinical-stage assets across therapeutic areas and modalities. That standard is the measure against which MindWalk holds every subsequent capability, including B cell Llama™ camelid nanobody discovery and the HYFT® biological intelligence infrastructure. The HYFT® system and LensAI™ platform were developed independently as a purpose-built AI architecture — not derived from the wet-lab programs, but subsequently integrated with them, and now embedded in every internal MindWalk program. The Knowledge Graph that underpins HYFT® — 660 million biological patterns, 25 billion relationships, refined over 20 years of curation — is not a general-purpose AI substrate trained on public data. It is a function-aware representation of biological sequence space, built on biological pattern recognition derived from the breadth of the global biosphere, and now operating in direct integration with the wet-lab discovery workflows that produced these programs. “Before AI was a hypothesis in life sciences, our scientists were generating the molecules that are now in clinical trials at our partners. That history is not a credential we display — it is a standard we hold ourselves to. When we bring a new capability into this organization, the question is always the same: can it meet the bar that wet-lab discovery set? HYFT® and LensAI™ were built by world-class scientists pursuing a singular focus: creating the most rigorous biological representation system ever developed. We integrated them because they cleared that bar. The result is a discovery organization where the biology and the AI interrogate each other — and where neither would be as good without the other.” — Dr. Jennifer Bath, PhD, Chief Executive Officer and President, MindWalk Holdings Corp. KEY FACTS 10 programs in active Phase 1–3 clinical trials; over 20 discovery-originated programs documented in total Clinical-stage programs include: ANX005 (Annexon Biosciences, Phase 3, Guilláin-Barré Syndrome, FDA Breakthrough Therapy designation); ARGX-119 (argenx, Phase 2/3, Congenital Myasthenic Syndrome); vudalimab / XmAb20717, XmAb306, XmAb808 (Xencor, Phase 1–2, solid tumors); CIT-013 (Citryll BV, Phase 2, rheumatoid arthritis and hidradenitis suppurativa); PMN310 (ProMIS Neurosciences, Phase 1b, Alzheimer’s disease); CLN-619 (Cullinan Oncology, Phase 1, solid tumors); OR502 (OncoResponse, Phase 1/2, solid tumors) Partners and collaborators include: Annexon Biosciences, argenx (NASDAQ: ARGX), Xencor (NASDAQ: XNCR), Citryll BV, ProMIS Neurosciences, Cullinan Oncology (NASDAQ: CGEM), OncoResponse, Sanofi Pasteur, Janssen Vaccines (Johnson & Johnson), Michael J. Fox Foundation, Perseus Science / ChemBio, IDEXX Laboratories (NASDAQ: IDXX) Discovery capability: Proprietary wet-lab antibody discovery across multiple modalities and species, including camelid VHH nanobody discovery via the B cell Llama™ platform — operating from MindWalk’s antibody discovery site in Victoria, British Columbia Biological intelligence infrastructure: HYFT® and LensAI™ were developed independently as a purpose-built AI architecture — built on biological pattern recognition derived from the breadth of the global biosphere — and subsequently integrated with MindWalk’s wet-lab discovery engine. The Knowledge Graph indexes 660 million biological patterns and 25 billion relationships, refined over 15 years of curation — enriching biological data at ingestion and compounding in analytical value with every program run on the platform. Publication record: Over 400 peer-reviewed publications and patents, originally published under ImmunoPrecise Antibodies (NASDAQ: IPA), Modiquest Research, and related entities, now operating as MindWalk Holdings Corp. (NASDAQ: HYFT) — reflecting a consistent scientific output across therapeutic areas, modalities, and discovery disciplines. Independent analysis has identified data structure and orchestration as the gating factors for enterprise AI value and named drug discovery as the highest-consequence AI application environment — the category where reliability is paramount and the cost of a wrong answer is too high to absorb. MindWalk occupies that layer for life sciences. The HYFT® representation layer enriches biological data at ingestion and compounds in analytical value with every program run on the platform. That compounding is not a product claim. It is an architectural consequence of a substrate built on biological pattern recognition derived from the breadth of the global biosphere — and now operating in direct integration with the wet-lab discovery workflows that produced these programs. The Company will provide further updates on its biological intelligence infrastructure, commercial programs, and platform development in the coming months. Access the report: Discovery-to-Clinic ABOUT MINDWALK HOLDINGS CORP. MindWalk Holdings Corp. (NASDAQ: HYFT) is a bio-native AI company building the biological intelligence infrastructure that life sciences AI and agentic AI require. Its proprietary HYFT® system functions as the AI-ready data substrate for life sciences — a function-aware representation organized around HYFT pattern-objects that span sequence and structural biology, refined over 20 years of curation by a continuously evolving Knowledge Graph of 660 million biological patterns and 25 billion relationships, that enriches data at ingestion and compounds in analytical value with every program run on the platform. The LensAI™ platform operates on this infrastructure to enable target discovery, candidate diligence, and portfolio decision support, and to host the agentic AI workflows pharma is racing to deploy. MindWalk’s architecture is designed so that the HYFT® representation layer — not any individual AI model — is the durable, compounding competitive asset. The HYFT® system and LensAI™ platform are fully integrated with MindWalk’s antibody discovery engine, operating in direct integration with the wet-lab workflows that have consistently produced clinical-stage assets for partners across therapeutic areas and modalities. The Company operates its antibody discovery laboratory in Victoria, British Columbia; its biological AI and technology operations through BioStrand in Belgium; and United States offices in Fargo, North Dakota, Minneapolis, Minnesota, and Boston, Massachusetts. Trademarks: HYFT®, LensAI™, HYFT Base™, HYFT Matrix™, HYFT Prime™, B cell Llama™, B Cell Select® are trademarks of MindWalk Holdings Corp. or its subsidiaries. All other trademarks are the property of their respective owners. FORWARD-LOOKING STATEMENTS This press release contains forward-looking statements within the meaning of applicable United States and Canadian securities laws. Forward-looking statements are often identified by terms such as “expects,” “intends,” “plans,” “anticipates,” “believes,” “estimates,” “targets,” or similar expressions, or by statements that certain actions, events, or results are expected to occur or be achieved. Forward-looking statements in this press release include, without limitation, statements regarding: the continuation and advancement of partner-owned clinical programs derived from MindWalk antibody discovery work; the characterization of MindWalk’s antibody discovery platform lineage and its translational record; the expected concurrent advancement of MindWalk’s B cell Llama™ camelid nanobody platform and the HYFT® / LensAI™ AI-native platform; the Company’s ability to apply native-repertoire wet-lab discovery and AI-native discovery to produce partner clinical-stage assets in the future; and statements regarding the competitive, structural, or functional characteristics and compounding value of the HYFT® biological pattern system and LensAI™ platform. Past success of one platform generation does not ensure clinical or commercial success of any other generation, including AI-native discovery. Forward-looking statements are based on management’s current expectations and assumptions and are subject to known and unknown risks, uncertainties, and other factors that may cause actual results to differ materially, including: risks relating to clinical trial outcomes at partner companies; partner program continuation or discontinuation; regulatory determinations; competition; intellectual property risks; the technical performance of AI-based discovery methods; and capital markets conditions. Additional information is available in MindWalk’s Annual Report on Form 20-F and other filings on SEDAR+ (sedarplus.ca) and EDGAR (sec.gov/edgar). Except as required by law, MindWalk undertakes no obligation to update any forward-looking statement. Nothing in this press release constitutes investment advice. This press release does not constitute an offer to sell or the solicitation of an offer to buy any securities. View source version on businesswire.com: https://www.businesswire.com/news/home/20260518834439/en/ Investor Relations Contact
Louie Toma, CPA, CFA
Managing Director, CoreIR
investors@mindwalkai.com Original: The Biology Came First.
US Market News
3月前
MindWalk Holdings Corp. publie ses résultats financiers du troisième trimestre 2026March 13, 2026 2:39 PM
Business Wire
Troisième trimestre consécutif de croissance des revenus en glissement annuel | Premier contrat annuel d'entreprise pour la plateforme LensAI™ | Lancement de la plateforme B cell Llama™ de découverte de nanocorps
MindWalk Holdings Corp. (Nasdaq : HYFT), une société d'IA bio-native axée sur la découverte de produits biologiques et le développement de médicaments optimisé par l'IA, annonce aujourd'hui ses résultats financiers pour le troisième trimestre de l'exercice 2026, clos le 31 janvier 2026. MindWalk tiendra sa téléconférence sur les résultats du troisième trimestre de l'exercice 2026 aujourd'hui à 10h30, heure de l'Est.
Le chiffre d'affaires du T3 s'établit à 4,2 millions de dollars, soit une augmentation de 52 % par rapport aux 2,7 millions de dollars du T3 de l'exercice 2025, marquant ainsi le troisième trimestre consécutif de croissance du chiffre d'affaires de MindWalk en glissement annuel. Le chiffre d'affaires aux États-Unis a doublé en glissement annuel pour atteindre 2,6 millions de dollars. Le plus grand client d'IA d'entreprise de la société a signé un contrat de plateforme LensAI d'un an, le premier contrat de revenu récurrent pour la plateforme dans l'histoire de la société, faisant ainsi passer une partie du chiffre d'affaires de MindWalk de revenus basés sur des projets à des revenus contractuels et récurrents.
« Ce trimestre, MindWalk a enregistré sa troisième hausse consécutive du chiffre d'affaires en glissement annuel et a fait avancer trois programmes de pipeline vers des lectures de données. Le chiffre d'affaires aux États-Unis a doublé en glissement annuel, reflétant notre orientation stratégique délibérée sur l'Amérique du Nord, y compris l'établissement d'opérations de services biologiques dans la région de Boston et de Cambridge et l'investissement commercial continu dans ce marché. Récemment, notre plus grand client d'IA d'entreprise a signé un contrat d'un an pour la plateforme LensAI, le premier du genre pour nous. LensAI est activement déployé dans l’ensemble de notre clientèle, et il s’agit d’une structure contractuelle que nous développons. »
— Dre Jennifer Bath, CEO et présidente, MindWalk Holdings Corp.
Faits financiers saillants du T3 2026
Indicateur
T3 2026
Commentaire
Chiffre d'affaires du T3 2026
4,2 millions $
vs 2,7 millions $ au T3 2025 (+52 %)
Chiffre d'affaires aux États-Unis
2,6 millions $
vs 1,3 million $ au T3 2025 (doublé en glissement annuel)
Chiffre d'affaires à ce jour (neuf mois)
11,4 millions $
vs 7,9 millions $ pour la même période de l'exercice précédent (+45 %)
Marge brute à ce jour
58 %
vs 53 % pour la même période de l'exercice précédent (+5 pp)
Marge brute du T3
59 %
vs 65 % pour la même période de l'exercice précédent
Perte nette issue des opérations poursuivies (T3)
3,9 millions $
vs 22,0 millions au T3 2025 (y compris 21,2 millions $ de dépréciation)
Trésorerie et équivalents de trésorerie
14,2 millions $
au 31 janvier 2026
Tous les chiffres sont en dollars canadiens. Relatif à la poursuite des activités, sauf indication contraire. Préparé conformément aux IFRS.
Faits saillants opérationnels et de la plateforme
Plateforme et commercial
Premier contrat pour la plateforme LensAI d'un an signé avec le plus grand client d'IA d'entreprise de MindWalk ; chiffre d'affaires comptabilisé mensuellement
Les services de la plateforme LensAI sont fournis directement aux clients dans toutes les opérations MindWalk
Le chiffre d'affaires pour les États-Unis a doublé en glissement annuel, reflétant l'orientation stratégique délibérée de la société sur l'Amérique du Nord, où la demande de produits biologiques optimisés par l’IA est concentrée et où l’environnement réglementaire est de plus en plus favorable aux partenaires nationaux. Cette orientation stratégique comprenait l'établissement d'opérations de services biologiques dans la région de Boston et de Cambridge et a orienté la décision de la société de céder ses opérations européennes en faveur de la croissance nord-américaine.
Lancement de la plateforme B cell Llama™
MindWalk annonce le lancement de B cell Llama™, une plateforme de découverte de nanocorps conçue sur l'isolement d'une cellule B des lamas immunisés. Les nanocorps VHH n’ont pas de chaîne légère, ce qui élimine le problème de l’appairage des chaînes qui a historiquement limité le développement d’anticorps bispécifiques et multispécifiques, un goulot d’étranglement reconnu sur un marché qui devrait dépasser 50 milliards de dollars d’ici à 2030.
MindWalk possède une expertise approfondie en nanocorps VHH construite après des années de travaux de découverte de produits biologiques. Une étude évaluée par des pairs et financée par des subventions publiée dans Biomacromolecules (American Chemical Society), menée en collaboration avec l'Université de technologie d'Eindhoven et le Centre médical de l'Université Radboud, présente de nouvelles conclusions :
Neutralisation démontrée d'une variante virale contre laquelle aucune thérapie d'anticorps cliniquement approuvée n'a montré d'activité
La molécule présentant l’affinité de liaison la plus forte dans les essais n’a produit aucune activité fonctionnelle, ce qui explique pourquoi la sélection des candidats fondée sur la fonction, et non l’affinité seule, est essentielle plus tôt dans le processus de découverte.
MindWalk détient le premier droit de commercialiser la propriété intellectuelle développée conjointement dans le cadre de la collaboration
Programme de vaccination contre la dengue
La dengue infecte 390 millions de personnes chaque année et est considérée comme l'une des dix principales menaces pour la santé mondiale par l'OMS. Il n'existe pas de vaccin contre la dengue approuvé par la FDA disponible aux États-Unis. Deux vaccins ont été mis le marché, et aucun ne génère d'immunité équilibrée pour les quatre sérotypes, le problème central non résolu en vaccinologie contre la dengue. L'approche de MindWalk identifie un seul épitope conservé partagé entre les quatre sérotypes, conçu pour remédier à cet échec au niveau de la conception.
Achèvement des études d'immunisation in vivo ; validation de la liaison, confirmant que les animaux immunisés ont produit des anticorps ciblant spécifiquement l’épitope de sérotype croisé conservé, avec des résultats attendus cette semaine
Après confirmation de liaison, le programme passe à l'examen des tests de neutralisation avec un collaborateur tiers indépendant pour évaluer la capacité du vaccin à neutraliser les sérotypes de la dengue
LensAI a identifié un seul épitope discontinu conservé dans les quatre sérotypes de la dengue, une cible non détectée par les outils conventionnels d’alignement séquentiel
Programme GLP-1
Activation in vitro du récepteur GLP-1 confirmée par un test indépendant effectué par un tiers ; les résultats démontrent une activité par rapport au sémaglutide, la thérapie GLP-1 leader sur le marché avec environ 29 milliards de dollars de ventes mondiales combinées en 2024.
Un traitement à double voie a été identifié, reliant la biologie du GLP-1 à une seconde voie de longévité non-chevauchante
Le programme progresse grâce aux conseils d'un important collaborateur pharmaceutique possédant une expertise reconnue dans ce domaine, les prochaines étapes confirmant l'élargissement des données in vitro, y compris des tests de stabilité, suivis d'une validation in vivo des profils d'innocuité.
Programme antigrippal
LensAI a maintenant examiné plus de deux mille séquences de grippe très diverses couvrant les types A et B, y compris les séquences d'origine aviaire et porcine, identifiant une seule caractéristique biologique conservée présente dans toutes les séquences analysées
programme progresse dans la fabrication du candidat principal in silico destiné à être utilisé dans les études de neutralisation, afin d’évaluer la capacité du vaccin à prévenir l’infection.
Financement d'actifs
Des conseillers juridiques et financiers ont été engagés pour concevoir des véhicules de financement structurés au niveau de l’actif dans l’ensemble du portefeuille propriétaire de MindWalk (y compris GLP-1, dengue et grippe) permettant des investissements ciblés au niveau du programme tout en préservant les fonds propres de la société mère
Téléconférence et webdiffusion
La webdiffusion en direct aura lieu le jeudi 12 mars 2026, à 10h30, heure de l'Est.
La téléconférence sera retransmise en direct sur le web et pourra être rediffusée via un lien fourni dans la section Événements des pages dédiées aux relations avec les investisseurs de la société à l’adresse suivante :
https://ir.mindwalkai.com/events-and-presentations/default.aspx
* Informations sur la webdiffusion *
Titre de l'événement : MindWalk Holdings Corp. – Third Quarter Fiscal Year 2026 Financial Results
Date de l'événement : 12 mars 2026, 10h30 heure de l'Est (États-Unis et Canada) (4h00 GMT)
URL des participants : https://events.q4inc.com/attendee/486881652
Pour suivre l'événement par téléphone :
États-Unis / international, numéro payant +1 (646) 307-1963
États-Unis, appel gratuit (800) 715-9871
Canada - Toronto (647) 932-3411
Canada - Toll-Free (800) 715-9871
Identifiant de la conférence : 3224490
Toute personne suivant la téléconférence est invitée à lire les rapports périodiques de la société disponibles sur le profil de l’entreprise sur www.sedarplus.ca et sur www.sec.gov, y compris la discussion des facteurs de risque et des résultats historiques des opérations et de la situation financière dans ces rapports.
À propos de MindWalk Holdings Corp.
MindWalk Holdings Corp. (Nasdaq : HYFT) est une société d'IA bio-native axée sur la découverte de produits biologiques et le développement de médicaments optimisé par l'IA. Le système de modèles biologiques HYFT® et la plateforme LensAI™ de la société fonctionnent sur la couche fonctionnelle invariante des séquences biologiques, les sous-séquences conservées essentielles à la fonction biologique, permettant la découverte de cibles, de candidats et d'informations auxquels les approches conventionnelles basées sur les séquences ne peuvent pas accéder. MindWalk opère par l'intermédiaire de filiales telles que MindWalk Biologics (Victoria, C.-B.), BioStrand (Belgique) et Talem Therapeutics (Dakota du Nord).
Déclarations prospectives
Le présent communiqué de presse contient des déclarations prospectives au sens des lois sur les valeurs mobilières applicables aux États-Unis et au Canada. Les déclarations prospectives sont souvent identifiées par des mots tels que « s’attend à », « a l'intention de », « planifie », « anticipe », « pense », « estime », « cible », « cherche à », « potentiel » ou expressions similaires, ou par des déclarations selon lesquelles certaines actions, événements ou résultats sont censés se produire ou être atteints.
Les déclarations prospectives contenues dans le présent communiqué de presse comprennent, sans s'y limiter, des déclarations concernant : l'interprétation et l'importance des observations découlant de l'application de la technologie HYFT® de la société ; l'identification, la caractérisation et la pertinence des modèles fonctionnels conservés et de la contiguïté fonctionnelle ; l'hypothèse que de tels modèles peuvent soutenir une conception rationnelle vers des immunogènes largement protecteurs, y compris dans les programmes de dengue et de grippe de la société ; la pertinence de la contiguïté fonctionnelle pour l'intelligence concurrentielle, la stratégie de propriété intellectuelle, le développement commercial et la prise de décision en matière de portefeuille ; le rôle prévu de l’analyse HYFT dans l’évaluation de la concurrence fonctionnelle, de l’exposition de la PI ou du risque de portefeuille ; l'intégration de HYFT au sein de la plateforme plus large de gestion des données et de raisonnement biologique de la société ; la portée, le calendrier et les résultats d’éventuelles activités de validation futures ; la croissance prévue des revenus, la commercialisation de la plateforme, les tendances des marges brutes et l'évolutivité des engagements de la plateforme LensAI™ ; la transition attendue des revenus liés aux projets vers les revenus contractuels et récurrents ; le calendrier, la conception et les résultats des activités de développement préclinique et clinique dans l'ensemble des programmes pipeliniers de la société, y compris les résultats attendus des tests de confirmation de liaison et de neutralisation multisérotypes pour le programme de vaccination contre la dengue et l'importance potentielle des résultats in vitro de l'agoniste des récepteurs GLP-1 par rapport au sémaglutide ; la portée et l'utilité prévues de la plateforme B cell Llama™ de découverte de nanocorps et sa pertinence pour le marché des thérapies bispécifiques, multispécifiques et CAR-T ; la conception, la structure et l'achèvement des véhicules de financement au niveau de l'actif pour les programmes exclusifs de la société, y compris le GLP-1, la dengue, la grippe et la plateforme B cell Llama™ ; et la capacité de la société à poursuivre, structurer ou compléter des investissements stratégiques, des collaborations, des arrangements commerciaux, des transactions de partenariat ou des opportunités de licence liées aux technologies ou programmes HYFT.
Les déclarations prospectives sont fondées sur les attentes, les hypothèses et les projections actuelles de la direction concernant les événements futurs et le rendement de la société. Les déclarations prospectives impliquent des risques connus et inconnus, des incertitudes et d'autres facteurs qui font en sorte que les résultats, les performances ou les réalisations réels diffèrent considérablement de ceux exprimés ou implicites. Ces facteurs comprennent, entre autres : la nature préliminaire et exploratoire des analyses informatiques et des observations in silico ; les limites des données, des données d'entrée ou des hypothèses analytiques disponibles ; le risque que des études de laboratoire, expérimentales ou de validation ultérieures ne reproduisent pas ou ne corroborent pas les observations rapportées ; incertitude quant à la pertinence biologique, à la robustesse ou à la généralisabilité des modèles fonctionnels identifiés ; le risque que les résultats in vitro , y compris les observations concernant l'activation des récepteurs GLP-1 par rapport au sémaglutide, ne se traduisent pas par des résultats in vivo ou cliniques ; le risque que les résultats du programme de neutralisation de la dengue, y compris la capacité d'obtenir une immunité équilibrée entre les sérotypes, ne soient pas atteints ou fassent l'objet d'une amélioration dépendante des anticorps ou d'autres résultats immunologiques défavorables ; les risques inhérents à la recherche et au développement thérapeutiques, y compris les défis liés à la traduction, à la validation, à la fabrication, à l'innocuité, à l’immunogénicité, à l’amplitude, à la durabilité ou à l’efficacité ; le risque que les décisions futures en matière de développement soient retardées, modifiées ou abandonnées ; les exigences et les incertitudes réglementaires ; la dépendance à l’égard de collaborateurs tiers, de laboratoires, de prestataires de services et de sources de données ; les risques en matière de propriété intellectuelle, y compris la capacité d'obtenir, de maintenir, de défendre et de faire respecter des brevets et d'autres droits de propriété ; développements concurrentiels ; la disponibilité, le calendrier et les modalités des instruments de financement au niveau des actifs ou d’autres solutions de financement, y compris le risque que ces structures ne puissent pas être achevées ou achevées à des conditions acceptables ; la capacité de conclure, de maintenir ou de faire respecter des collaborations, des accords de partenariat ou des accords commerciaux à des conditions acceptables ; et des conditions économiques, de marché, géopolitiques ou réglementaires plus larges.
Des informations supplémentaires sur ces risques et incertitudes ainsi que sur d'autres risques et incertitudes sont présentées dans le rapport annuel de la société sur le formulaire 20-F, tel que modifié, pour l'exercice clos le 30 avril 2025, disponible sur le profil SEDAR+ de la société à l'adresse www.sedarplus.ca et sur le profil EDGAR à l'adresse www.sec.gov/edgar.
Le lecteur est prié de ne pas se fier indûment aux déclarations prospectives. Sauf si la loi applicable l'exige, la société ne s'engage pas à mettre à jour ou à réviser les déclarations prospectives pour refléter de nouvelles informations, des événements futurs ou autrement.
Le présent communiqué de presse ne constitue pas une offre de vente ni la sollicitation d'une offre d'achat de titres.
Tous les chiffres financiers sont déclarés en dollars canadiens et se rapportent aux activités poursuivies, sauf indication contraire. MindWalk prépare ses états financiers conformément aux normes internationales d'information financière (IFRS).
Le rapprochement de la perte nette et du BAIIA ajusté est présenté dans le tableau ci-dessous :
Trimestre clos au
31 janvier
2026
2025
(en milliers)
$
$
Perte nette
(3 930
)
(21 521
)
Impôts sur le revenu
(18
)
(3 013
)
Amortissements
218
705
Désactualisation
—
3
Dépréciation d'actifs
—
21 184
Gain (perte) de change réalisé(e)
64
48
Charges d'intérêts
56
227
Intérêts et autres revenus (charges)
(30
)
183
Perte sur cession d'Europe B.V.
53
—
Gain (perte) de change non réalisé(e)
266
(80
)
Charges sur actions
257
70
BAIIA ajusté
(3 064
)
(2 194
)
*Tous les chiffres financiers sont en dollars canadiens (CAD), sauf indication contraire.
MINDWALK HOLDINGS CORP.
ÉTATS CONSOLIDÉS DE PERTES ÉTENDUES
(non vérifiés, en dollars canadiens)
Trimestre clos au
31 janvier
Neuf mois clos au
31 janvier
(en milliers, sauf pour les données en actions)
2026
$
2025
$
2026
$
2025
$
CHIFFRE D'AFFAIRES
4 158
2 728
11 443
7 879
COÛT DES VENTES
1 694
967
4 790
3 740
BÉNÉFICE BRUT
2 464
1 761
6 653
4 139
CHARGES
R&D
1 214
914
3 362
3 385
Ventes et marketing
1 800
1 138
4 409
2 754
Frais généraux et administratifs
3 124
2 864
9 490
9 072
Amortissement des immobilisations incorporelles
—
520
—
1 530
Dépréciation d'actifs
—
21 184
—
21 184
6 138
26 620
17 261
37 925
Perte avant autres revenus (charges) et impôts sur le revenu
(3 674
)
(24 859
)
(10 608
)
(33 786
)
AUTRES REVENUS (CHARGES)
Désactualisation
—
(3
)
—
(5
)
Revenus des subventions
15
—
34
138
Revenu d'intérêts et autres (charges)
30
(183
)
70
(302
)
Perte sur cession d'Europe B.V.
(53
)
—
(511
)
—
Perte de change non réalisée
(266
)
80
(305
)
(164
)
(274
)
(106
)
(712
)
(333
)
Perte avant impôt sur le revenu
(3 948
)
(24 965
)
(11 320
)
(34 119
)
Impôts sur le revenu
18
3 013
83
4 408
PERTE NETTE DES OPÉRATIONS POURSUIVIES
(3 930
)
(21 952
)
(11 237
)
(29 711
)
REVENU NET DES OPÉRATIONS ABANDONNÉES
—
431
1 153
1 638
PERTE NETTE POUR LA PÉRIODE
(3 930
)
(21 521
)
(10 084
)
(28 073
)
AUTRES REVENUS ÉTENDUS (PERTE)
Éléments qui seront reclassés ultérieurement en perte
Différence de change lors de la conversion d'opérations à l'étranger
(224
)
471
(83
)
376
PERTE ÉTENDUE POUR LA PÉRIODE
(4 154
)
(21 050
)
(10 167
)
(27 697
)
PERTE PAR ACTION DES OPÉRATIONS POURSUIVIES — DE BASE ET DILUÉE
(0,08
)
(0,67
)
(0,24
)
(1,01
)
REVENU PAR ACTION DES OPÉRATIONS ABANDONNÉES — DE BASE ET DILUÉ
—
0,01
0,02
0,06
NOMBRE MOYEN PONDÉRÉ D'ACTIONS EN CIRCULATION
46 515 653
32 851 233
46 274 659
29 367 687
MINDWALK HOLDINGS CORP.
ÉTATS CONSOLIDÉS DE LA SITUATION FINANCIÈRE
(non vérifiés, en dollars canadiens)
(en milliers)
31 janvier
2026
$
30 avril
2025
$
ACTIF
Actif à court terme
Trésorerie
14 072
10 665
Montants exigibles, nets
1 883
4 115
Créances fiscales
190
143
Inventaire
490
2 095
Recettes non facturées
936
548
Dépenses payées d'avance
1 244
1 188
18 815
18 754
Encaisse affectée
126
126
Dépôt sur l'équipement
26
502
Immobilisations corporelles
4 020
15 762
Immobilisations incorporelles
—
1 067
Écart d'acquisition
—
8 230
Total de l'actif
22 987
44 441
PASSIF
Passif à court terme
Comptes débiteurs et charges à payer
3 334
5 283
Recettes reportées
941
1 090
Impôts sur le revenu à payer
328
475
Baux
427
1 850
Paiements d'acquisition différés
—
314
5 030
9 012
Baux
3 097
11 553
Impôt différé sur le revenu
—
250
Total du passif
8 127
20 815
CAPITAUX PROPRES
Capital social
137 293
136 371
Excédent de contribution
13 298
12 833
Pertes cumulées et autres pertes étendues
3 133
3 216
Déficit cumulé
(138 864
)
(128 794
)
14 860
23 626
Total passif et capitaux propres
22 987
44 441
MINDWALK HOLDINGS CORP.
ÉTATS CONSOLIDÉS DES FLUX DE TRÉSORERIE
Pour les neuf mois clos au 31 janvier 2026 et 2025
(non vérifiés, en dollars canadiens)
(en milliers)
2026
$
2025
$
Activités d'exploitation :
Perte nette pour la période
(10 084
)
(28 073
)
Éléments n'affectant pas la trésorerie :
Amortissements
1 366
4 206
Impôts différés sur le revenu
12
(3 935
)
Désactualisation
—
8
Taux de change
360
159
Gain sur investissement
—
(7
)
Perte sur la vente d'Europe B.V.
511
—
Dépréciation d'actifs
—
21,184
Charges en actions
465
392
(7 370
)
(6 066
)
Variations de fonds de roulement hors trésorerie liées aux opérations :
Montants à recevoir
(929
)
306
Inventaire
(50
)
253
Recettes non facturées
(1 053
)
(759
)
Dépenses payées d'avance
(839
)
388
Comptes créditeurs et charges à payer
(929
)
(87
)
Impôts sur les ventes et sur le revenu à payer et à recevoir
625
(298
)
Recettes reportées
490
993
Encaisse nette utilisée dans les activités d'exploitation
(10 055
)
(5 270
)
Activités d'investissement :
Achats de biens et d'équipements
(387
)
(440
)
Paiements d'acquisition différés
(312
)
—
Produit de la vente d'Europe B.V.
14 255
—
Encaisse nette utilisée dans les activités d'investissement
13 556
(440
)
Activités de financement :
Produit de l'émission d'actions, net des coûts de transaction (frais ATM)
926
12 211
Remboursement des baux
(526
)
(1 142
)
Produit de l’émission de débentures, déduction faite des coûts de transaction
—
4 242
Encaisse nette issue des activités de financement
400
15 311
Augmentation de la trésorerie au cours de la période
3 901
9 601
Change
(494
)
(141
)
Trésorerie, début de période
10 791
3 545
Trésorerie, fin de période
14 198
13 005
La trésorerie comprend :
Trésorerie
14 072
12 915
Encaisse affectée
126
90
14 198
13 005
Trésorerie payée au titre des intérêts
—
—
Trésorerie payée au titre de l'impôt sur le revenu
—
—
Encaisse issue des activités abandonnées :
Encaisse nette utilisée dans les activités d'exploitation
777
1 587
Encaisse nette utilisée dans les activités d'investissement
(100
)
(253
)
Encaisse nette utilisée dans les activités de financement
(359
)
(638
)
Source: MindWalk Holdings Corp.
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Consultez la version source sur businesswire.com : https://www.businesswire.com/news/home/20260312540743/fr/
Relations avec les investisseurs
Louie Toma, CPA, CFA
Directeur général, CoreIR
investors@mindwalkai.com
Original: MindWalk Holdings Corp. publie ses résultats financiers du troisième trimestre 2026
US Market News
3月前
MindWalk Holdings Corp. Reports Q3 Fiscal 2026 Financial ResultsMarch 12, 2026 8:31 AM
Business Wire
Third Consecutive Quarter of Year-Over-Year Revenue Growth | First Annual Enterprise LensAI™ Platform Contract | Launch of B cell Llama™ Nanobody Discovery Platform
MindWalk Holdings Corp. (Nasdaq: HYFT), a Bio-Native AI company focused on biologics discovery and AI-driven drug development, today reported financial results for the third quarter of fiscal year 2026, ended January 31, 2026. MindWalk will host its Q3 Fiscal 2026 Earnings Call today at 10:30 AM Eastern Time.
Revenue for Q3 was $4.2 million, a 52 percent increase from $2.7 million in Q3 fiscal 2025, marking MindWalk's third consecutive quarter of year-over-year revenue growth. US revenue doubled year over year to $2.6 million. The Company's largest enterprise AI client signed a one-year LensAI platform contract, the first contracted, recurring platform revenue agreement in the Company's history, shifting a part of MindWalk's revenue from project-based to contracted and recurring.
“This quarter, MindWalk reported its third consecutive year-over-year revenue increase and advanced three pipeline programs toward data readouts. US revenue doubled year over year, reflecting our deliberate, strategic focus on North America, including the establishment of biologics services operations in the Boston and Cambridge area and ongoing commercial investment in that market. Recently, our largest enterprise AI client signed a one-year LensAI platform contract, the first of its kind for us. LensAI is actively being rolled out across our broader client base, and this is a contract structure we are scaling.”
— Dr. Jennifer Bath, CEO & President, MindWalk Holdings Corp.
Q3 Fiscal 2026 Financial Highlights
Metric
Q3 FY2026
Commentary
Q3 FY2026 Revenue
$4.2 million
vs. $2.7 million in Q3 FY2025 (+52%)
US Revenue
$2.6 million
vs. $1.3 million in Q3 FY2025 (doubled YoY)
YTD Revenue (9 months)
$11.4 million
vs. $7.9 million in prior year period (+45%)
YTD Gross Margin
58%
vs. 53% in prior year period (+5 pp)
Q3 Gross Margin
59%
vs. 65% in prior year period
Net Loss from Cont. Ops (Q3)
$3.9 million
vs. $22.0 million Q3 FY2025 (incl. $21.2M impairment)
Cash & Equivalents
$14.2 million
as of January 31, 2026
All figures in Canadian dollars. Relate to continuing operations unless otherwise stated. Prepared in accordance with IFRS.
Operational and Platform Highlights
Platform & Commercial
First enterprise one-year LensAI platform contract signed with MindWalk's largest enterprise AI client; revenue recognized monthly
LensAI platform services are delivered directly to clients across all MindWalk operations
US revenue doubled year over year, reflecting the Company's deliberate strategic focus on North America; where AI-driven biologics demand is concentrated and the regulatory environment is increasingly favorable to domestic partners. This strategic direction included the establishment of biologics services operations in the Boston and Cambridge area and guided the Company's decision to divest its European operations in favor of North American growth.
B cell Llama™ Platform Launch
MindWalk announces the launch of B cell Llama™, a nanobody discovery platform built on single B cell isolation from immunized llamas. VHH nanobodies carry no light chain, eliminating the chain-pairing problem that has historically limited bispecific and multispecific antibody development — a recognized bottleneck in a market projected to exceed $50 billion by 2030.
MindWalk has deep VHH nanobody expertise built over years of biologics discovery work. A peer-reviewed and grant-funded study published in Biomacromolecules (American Chemical Society), conducted in collaboration with Eindhoven University of Technology and Radboud University Medical Center, demonstrates new findings:
Demonstrated neutralization of a viral variant against which no clinically approved antibody therapies showed activity
The molecule with the strongest binding affinity in assays delivered zero functional activity — underscoring why function-based candidate selection, not affinity alone, is critical earlier in the discovery process.
MindWalk holds first right to commercialize the jointly developed intellectual property from the collaboration
Dengue Vaccine Program
Dengue infects 390 million people annually and is considered a top ten global health threat by the WHO. There is no FDA-approved dengue vaccine available in the United States. Two vaccines have reached market, with both failing to generate balanced immunity across all four serotypes, the central unsolved problem in dengue vaccinology. MindWalk's approach identifies a single conserved epitope shared across all four serotypes, designed to address that failure at the design level.
In vivo immunization studies complete; binding confirmation — confirming that immunized animals generated antibodies specifically targeting the conserved cross-serotype epitope — results anticipated this week
Upon binding confirmation, the program advances to pan neutralization testing with an independent third-party collaborator to assess the ability of the vaccine to neutralize across dengue serotypes
LensAI identified a single discontinuous epitope conserved across all four dengue serotypes — a target not detected by conventional sequence-alignment tools
GLP-1 Program
In vitro GLP-1 receptor activation confirmed by independent third-party assay; results demonstrate activity relative to semaglutide, the market-leading GLP-1 therapy with approximately $29 billion in combined global sales in 2024.
Dual-pathway regimen identified, linking GLP-1 biology to a second, non-overlapping longevity pathway
Program advancing with guidance from a large pharma collaborator with recognized expertise in this area, with next steps confirming expanded in vitro data including stability testing followed by in vivo validation of safety profiles.
Influenza Program
LensAI has now screened over two thousand highly diverse influenza sequences spanning influenza A and B types, including avian and swine-origin sequences, identifying a single conserved biological feature present across all sequences analyzed
Program advancing into manufacturing of the lead in silico candidate for use in neutralization studies – to assess the ability of the vaccine to prevent infection.
Asset Financing
Legal and financial advisors engaged to design structured, asset-level financing vehicles across MindWalk’s proprietary portfolio - including GLP-1, dengue, and influenza - enabling targeted program-level investment while preserving parent company equity
Conference Call and Webcast Details
The live webcast will take place on Thursday, March 12, 2026, at 10:30AM ET.
The conference call will be webcast live and available for replay via a link provided in the Events section of the Company’s IR pages at:
https://ir.mindwalkai.com/events-and-presentations/default.aspx
* Webcast Details *
Event Title: MindWalk Holdings Corp. – Third Quarter Fiscal Year 2026 Financial Results
Event Date: March 12, 2026, 10:30 AM (GMT-04:00) Eastern Time (US and Canada)
Attendee URL: https://events.q4inc.com/attendee/486881652
Participant Dial-in:
USA / International Toll +1 (646) 307-1963
USA - Toll-Free (800) 715-9871
Canada - Toronto (647) 932-3411
Canada - Toll-Free (800) 715-9871
Conference ID: 3224490
Anyone listening to the call is encouraged to read the company’s periodic reports available on the company’s profile at www.sedarplus.ca and www.sec.gov, including the discussion of risk factors and historical results of operations and financial condition in those reports.
About MindWalk Holdings Corp.
MindWalk Holdings Corp. (Nasdaq: HYFT) is a Bio-Native AI company focused on biologics discovery and AI-driven drug development. The Company’s proprietary HYFT® biological pattern system and LensAI™ platform operate on the invariant functional layer of biological sequence space — the conserved subsequences essential to biological function — enabling the discovery of targets, candidates, and insights that conventional sequence-based approaches cannot access. MindWalk operates through subsidiaries including MindWalk Biologics (Victoria, BC), BioStrand (Belgium), and Talem Therapeutics (North Dakota).
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of applicable United States and Canadian securities laws. Forward-looking statements are often identified by words such as "expects," "intends," "plans," "anticipates," "believes," "estimates," "targets," "seeks," "potential," or similar expressions, or by statements that certain actions, events, or results are expected to occur or be achieved.
Forward-looking statements in this press release include, without limitation, statements regarding: the interpretation and significance of observations derived from the application of the Company's HYFT® technology; the identification, characterization, and relevance of conserved functional patterns and functional adjacency; the hypothesis that such patterns may support rational design toward broadly protective immunogens, including in the Company's dengue and influenza programs; the relevance of functional adjacency to competitive intelligence, intellectual property strategy, business development, and portfolio decision-making; the intended role of HYFT-based analysis in evaluating functional competition, IP exposure, or portfolio risk; the integration of HYFT within the Company's broader data management and biological reasoning platform; the scope, timing, and outcome of potential future validation activities; anticipated revenue growth, platform commercialization, gross margin trends, and the scalability of LensAI™ platform engagements; the expected transition from project-based to contracted and recurring revenue; the timing, design, and outcome of preclinical and clinical development activities across the Company's pipeline programs, including the anticipated binding confirmation and multi-serotype neutralization testing results for the dengue vaccine program and the potential significance of the GLP-1 receptor agonist in vitro results relative to semaglutide; the anticipated scope and utility of the B cell Llama™ nanobody discovery platform and its relevance to the bispecific, multispecific, and CAR-T therapeutics market; the design, structure, and completion of asset-level financing vehicles for the Company's proprietary programs, including GLP-1, dengue, influenza, and B cell Llama™; and the Company's ability to pursue, structure, or complete strategic investments, collaborations, commercial arrangements, partnering transactions, or licensing opportunities related to HYFT-based technologies or programs.
Forward-looking statements are based on management's current expectations, assumptions, and projections about future events and Company performance. Forward-looking statements involve known and unknown risks, uncertainties, and other factors that cause actual results, performance, or achievements to differ materially from those expressed or implied. These factors include, among others: the preliminary and exploratory nature of computational analyses and in silico observations; limitations in available data, inputs, or analytical assumptions; the risk that subsequent laboratory, experimental, or validation studies do not replicate or support the reported observations; uncertainty regarding the biological relevance, robustness, or generalizability of identified functional patterns; the risk that in vitro results, including observations regarding GLP-1 receptor activation relative to semaglutide, do not translate to in vivo or clinical outcomes; the risk that dengue program neutralization results, including the ability to achieve balanced cross-serotype immunity, are not achieved or are subject to antibody-dependent enhancement or other adverse immunological outcomes; risks inherent in therapeutic research and development, including challenges related to translation, validation, manufacturability, safety, immunogenicity, breadth, durability, or efficacy; the risk that future development decisions are delayed, modified, or discontinued; regulatory requirements and uncertainties; dependence on third-party collaborators, laboratories, service providers, and data sources; intellectual property risks, including the ability to obtain, maintain, defend, and enforce patent and other proprietary rights; competitive developments; the availability, timing, and terms of asset-level financing vehicles or other financing alternatives, including the risk that such structures cannot be completed on acceptable terms or at all; the ability to enter into, maintain, or enforce collaborations, partnering arrangements, or commercial agreements on acceptable terms; and broader economic, market, geopolitical, or regulatory conditions.
Additional information about these and other risks and uncertainties is set out in the Company's Annual Report on Form 20-F, as amended, for the fiscal year ended April 30, 2025, available on the Company's SEDAR+ profile at www.sedarplus.ca and EDGAR profile at www.sec.gov/edgar.
Readers are cautioned not to place undue reliance on forward-looking statements. Except as required by applicable law, the Company undertakes no obligation to update or revise any forward-looking statements to reflect new information, future events, or otherwise.
This press release does not constitute an offer to sell or the solicitation of an offer to buy any securities.
All financial figures are reported in Canadian dollars and relate to continuing operations unless otherwise stated. MindWalk prepares its financial statements in accordance with International Financial Reporting Standards (IFRS).
The reconciliation of Net Loss to Adjusted EBITDA is presented in the table below:
Three months ended
January 31,
2026
2025
(in thousands)
$
$
Net loss
(3,930
)
(21,521
)
Income taxes
(18
)
(3,013
)
Amortization and depreciation
218
705
Accretion
—
3
Asset impairment
—
21,184
Foreign exchange realized gain (loss)
64
48
Interest expense
56
227
Interest and other income (expense)
(30
)
183
Loss on disposal of Europe B.V.
53
—
Unrealized foreign exchange gain (loss)
266
(80
)
Share-based expense
257
70
Adjusted EBITDA
(3,064
)
(2,194
)
*All financial figures are in Canadian Dollars (CAD) unless otherwise stated.
MINDWALK HOLDINGS CORP.
CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
(Unaudited - Expressed in Canadian dollars)
Three months ended
January 31,
Nine months ended
January 31,
(in thousands, except share data)
2026
$
2025
$
2026
$
2025
$
REVENUE
4,158
2,728
11,443
7,879
COST OF SALES
1,694
967
4,790
3,740
GROSS PROFIT
2,464
1,761
6,653
4,139
EXPENSES
Research and development
1,214
914
3,362
3,385
Sales and marketing
1,800
1,138
4,409
2,754
General and administrative
3,124
2,864
9,490
9,072
Amortization of intangible assets
—
520
—
1,530
Asset Impairment
—
21,184
—
21,184
6,138
26,620
17,261
37,925
Loss before other income (expenses) and income taxes
(3,674
)
(24,859
)
(10,608
)
(33,786
)
OTHER INCOME (EXPENSES)
Accretion
—
(3
)
—
(5
)
Grant income
15
—
34
138
Interest and other income (expense)
30
(183
)
70
(302
)
Loss on disposal of Europe B.V.
(53
)
—
(511
)
—
Unrealized foreign exchange loss
(266
)
80
(305
)
(164
)
(274
)
(106
)
(712
)
(333
)
Loss before income taxes
(3,948
)
(24,965
)
(11,320
)
(34,119
)
Income taxes
18
3,013
83
4,408
NET LOSS FROM CONTINUING OPERATIONS
(3,930
)
(21,952
)
(11,237
)
(29,711
)
NET INCOME FROM DISCONTINUED OPERATIONS
—
431
1,153
1,638
NET LOSS FOR THE PERIOD
(3,930
)
(21,521
)
(10,084
)
(28,073
)
OTHER COMPREHENSIVE INCOME (LOSS)
Items that will be reclassified subsequently to loss
Exchange difference on translating foreign operations
(224
)
471
(83
)
376
COMPREHENSIVE LOSS FOR THE PERIOD
(4,154
)
(21,050
)
(10,167
)
(27,697
)
LOSS PER SHARE FROM CONTINUING OPERATIONS– BASIC AND DILUTED
(0.08
)
(0.67
)
(0.24
)
(1.01
)
INCOME PER SHARE FROM DISCONTINUED OPERATIONS– BASIC AND DILUTED
—
0.01
0.02
0.06
WEIGHTED AVERAGE NUMBER OF SHARES OUTSTANDING
46,515,653
32,851,233
46,274,659
29,367,687
MINDWALK HOLDINGS CORP.
CONSOLIDATED STATEMENTS OF FINANCIAL POSITION
(Unaudited - Expressed in Canadian dollars)
(in thousands)
January 31,
2026
$
April 30,
2025
$
ASSETS
Current assets
Cash
14,072
10,665
Amounts receivable, net
1,883
4,115
Tax receivable
190
143
Inventory
490
2,095
Unbilled revenue
936
548
Prepaid expenses
1,244
1,188
18,815
18,754
Restricted cash
126
126
Deposit on equipment
26
502
Property and equipment
4,020
15,762
Intangible assets
—
1,067
Goodwill
—
8,230
Total assets
22,987
44,441
LIABILITIES
Current liabilities
Accounts payable and accrued liabilities
3,334
5,283
Deferred revenue
941
1,090
Income taxes payable
328
475
Leases
427
1,850
Deferred acquisition payments
—
314
5,030
9,012
Leases
3,097
11,553
Deferred income tax liability
—
250
Total liabilities
8,127
20,815
SHAREHOLDERS' EQUITY
Share capital
137,293
136,371
Contributed surplus
13,298
12,833
Accumulated other comprehensive loss
3,133
3,216
Accumulated deficit
(138,864
)
(128,794
)
14,860
23,626
Total liabilities and shareholders’ equity
22,987
44,441
MINDWALK HOLDINGS CORP.
CONSOLIDATED STATEMENTS OF CASH FLOWS
For the nine months ended January 31, 2026 and 2025
(Unaudited - Expressed in Canadian dollars)
(in thousands)
2026
$
2025
$
Operating activities:
Net loss for the period
(10,084
)
(28,073
)
Items not affecting cash:
Amortization and depreciation
1,366
4,206
Deferred income taxes
12
(3,935
)
Accretion
—
8
Foreign exchange
360
159
Gain on investment
—
(7
)
Loss on sale of Europe B.V.
511
—
Asset Impairment
—
21,184
Share-based expense
465
392
(7,370
)
(6,066
)
Changes in non-cash working capital related to operations:
Amounts receivable
(929
)
306
Inventory
(50
)
253
Unbilled revenue
(1,053
)
(759
)
Prepaid expenses
(839
)
388
Accounts payable and accrued liabilities
(929
)
(87
)
Sales and income taxes payable and receivable
625
(298
)
Deferred revenue
490
993
Net cash used in operating activities
(10,055
)
(5,270
)
Investing activities:
Purchases of property and equipment
(387
)
(440
)
Deferred acquisition payments
(312
)
—
Proceeds on sale of Europe B.V.
14,255
—
Net cash used in investing activities
13,556
(440
)
Financing activities:
Proceeds on share issuance, net of transaction costs (ATM fees)
926
12,211
Repayment of leases
(526
)
(1,142
)
Proceeds on debenture issuance, net of transaction costs
—
4,242
Net cash provided by financing activities
400
15,311
Increase in cash during the period
3,901
9,601
Foreign exchange
(494
)
(141
)
Cash – beginning of the period
10,791
3,545
Cash – end of the period
14,198
13,005
Cash is comprised of:
Cash
14,072
12,915
Restricted cash
126
90
14,198
13,005
Cash paid for interest
—
—
Cash paid for income tax
—
—
Cash from discontinued operations:
Net cash used in operating activities
777
1,587
Net cash used in investing activities
(100
)
(253
)
Net cash used in financing activities
(359
)
(638
)
Source: MindWalk Holdings Corp.
View source version on businesswire.com: https://www.businesswire.com/news/home/20260312858299/en/
Investor Relations Contact
Louie Toma, CPA, CFA
Managing Director, CoreIR
investors@mindwalkai.com
Original: MindWalk Holdings Corp. Reports Q3 Fiscal 2026 Financial Results
US Market News
4月前
MindWalk Applies HYFT® Technology to Detect Functional Adjacency Linked to Portfolio Risk in AI-Designed TherapeuticsJanuary 27, 2026 5:01 AM
Business Wire
MindWalk Holdings Corp. (NASDAQ:HYFT) (“MindWalk” or the “Company”), a Bio-Native AI therapeutic research and technology company, today announced an application of its proprietary HYFT® technology designed to identify functional adjacency - meaning different molecules can produce the same therapeutic effect even when sequence comparisons suggest they are unrelated - an emerging source of competitive, legal, and valuation risk in modern drug discovery that sequence-alignment-based analysis often fails to capture.
Using HYFT® technology, MindWalk found a shared biological “signature” in influenza that stays consistent even when the virus’s genetic code changes a lot. This supports MindWalk’s approach to designing vaccine targets aimed at broader protection across strains and shows how HYFT identifies meaningful similarities in biology even when molecules do not look alike at first glance.
“Functional adjacency is now one of the most under-appreciated risks in pharmaceutical R&D,” said Jennifer Bath, Ph.D., Chief Executive Officer of MindWalk. “If two molecules deliver the same biological effect, they may compete for the same patient, pursue similar regulatory labels, and undermine perceived differentiation even if their sequences appear unrelated. As AI accelerates protein design, teams can generate many distinct sequences that converge on the same functional outcome, increasing the likelihood of competitive overlap, IP vulnerability, and valuation compression. HYFT is intended to help identify this convergence early by evaluating similarity at the functional level, not only at the sequence level.”
The Functional Adjacency Problem: An Emerging IP Risk for Pharma
Functional adjacency, where distinct molecular entities produce the same biological effect despite limited or no sequence similarity, has emerged as a material legal, competitive, and valuation risk in pharmaceutical development. Recent U.S. patent decisions have increased scrutiny on broadly drafted, functionally defined claim scope and underscore the need for disclosure and support proportional to what a patent claims.
In Amgen v. Sanofi, the U.S. Supreme Court found certain broad, functionally defined antibody claims directed to PCSK9 inhibition invalid for lack of enablement, meaning the patent did not teach others how to make and use the full claimed scope without undue experimentation. The decision reinforced a critical reality for biologics, competitive overlap often follows functional equivalence, not sequence similarity, and durable patent protection requires enabling disclosure consistent with the breadth of the claim.
Similarly, in Juno Therapeutics v. Kite Pharma, the Federal Circuit found certain CAR-T claims invalid for lack of written description, meaning the patent did not adequately describe the full claimed class of binding elements. The court’s analysis highlighted the risk of claiming broad functional territory without sufficient support, such as representative examples and shared defining features, across the claimed range.
Together, these decisions reflect an industry shift:
Multiple molecules achieve the same therapeutic effect through different sequences
Sequence novelty alone often proves insufficient as a proxy for competitive or legal differentiation
Competitive landscapes, deal valuations, and IP strategies built primarily on sequence similarity may face increasing fragility
As AI-driven protein design accelerates, this challenge intensifies. High-throughput platforms rapidly explore functional space and produce diverse sequences that converge on similar activity, creating blind spots in competitive intelligence and asset valuation when evaluation relies heavily on sequence similarity alone. Functional adjacency is no longer theoretical; it is increasingly recognized as an economically material risk, and recent case law underscores its IP implications.
HYFT Technology: Functional Intelligence Beyond Sequence Alignment
HYFT technology is designed to help close this gap by identifying conserved functional patterns shaped by biophysical constraints such as structure, charge, and binding interactions, even when evolutionary relationships are unclear and sequence similarity is low.
“HYFT technology lets us step outside sequence thinking and identify a functional constraint influenza appears to preserve for infection,” said Dirk Van Hyfte, MD, Ph.D., Chief Technology Officer of MindWalk.
In MindWalk’s influenza study, HYFT-based analysis identified functional architecture that persisted despite viral mutation, showing how influenza can change its sequence while preserving features required for infection. The same principle applies to AI-designed therapeutics, where optimization can generate diverse sequences that converge on similar functional outcomes.
HYFT technology is designed to help organizations evaluate competition, IP exposure, and portfolio risk based on functional similarity, where clinical and commercial overlap often occurs.
Strategic Implications for Pharma and Investors
The influenza observation, together with MindWalk’s previously disclosed HYFT-enabled dengue epitope program, shows HYFT as a cross-pathogen platform for identifying conserved functional design rules in biology, even when targets look different at the sequence level.
Taken together, these programs support the view that HYFT is not a single-asset discovery tool. It is positioned as a scalable strategic intelligence capability within MindWalk’s broader data management and biological reasoning platform.
As deployed, HYFT is intended to help pharmaceutical and biotechnology organizations:
Identify potential functional competitors earlier, including AI-designed or convergently evolved assets that sequence-based comparisons may miss
Strengthen in-licensing and M&A diligence efforts by assessing functional overlap, not only sequence similarity
Inform patent strategy under heightened scrutiny of function-based claims by grounding how functional space is characterized and supported
Improve R&D portfolio choices and capital allocation by prioritizing differentiated opportunities and identifying crowded functional areas earlier
MindWalk plans to engage pharmaceutical, biotechnology, and other organizations to explore collaborations and commercial arrangements that deploy HYFT-based functional intelligence across discovery, diligence, and portfolio decision workflows. This is designed to integrate with MindWalk’s end-to-end data platform, which unifies sequence, structure, function, and literature within a single operational framework.
This approach is designed to shift organizations from backward-looking analysis to forward-looking functional decision-making, aligning scientific discovery, competitive intelligence, IP strategy, and capital deployment as AI accelerates therapeutic design.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of applicable United States and Canadian securities laws. Forward-looking statements are often identified by words such as “expects,” “intends,” “plans,” “anticipates,” “believes,” “estimates,” “targets,” “seeks,” “potential,” or similar expressions, or by statements that certain actions, events, or results are expected to occur or be achieved.
Forward-looking statements in this press release include, without limitation, statements regarding: the interpretation and significance of observations derived from the application of the Company’s HYFT® technology; the identification, characterization, and relevance of conserved functional patterns and functional adjacency; the hypothesis that such patterns may support rational design toward broadly protective influenza immunogens; the relevance of functional adjacency to competitive intelligence, intellectual property strategy, business development, and portfolio decision-making; the intended role of HYFT-based analysis in evaluating functional competition, IP exposure, or portfolio risk; the integration of HYFT within the Company’s broader data management and biological reasoning platform; the scope, timing, and outcome of potential future validation activities; and the Company’s ability to pursue, structure, or complete strategic investments, collaborations, commercial arrangements, partnering transactions, or licensing opportunities related to HYFT-based technologies or programs.
Forward-looking statements are based on management’s current expectations, assumptions, and projections about future events and Company performance. Forward-looking statements involve known and unknown risks, uncertainties, and other factors that cause actual results, performance, or achievements to differ materially from those expressed or implied. These factors include, among others: the preliminary and exploratory nature of computational analyses and in silico observations; limitations in available data, inputs, or analytical assumptions; the risk that subsequent laboratory, experimental, or validation studies do not replicate or support the reported observations; uncertainty regarding the biological relevance, robustness, or generalizability of identified functional patterns; risks inherent in therapeutic research and development, including challenges related to translation, validation, manufacturability, safety, immunogenicity, breadth, durability, or efficacy; the risk that future development decisions are delayed, modified, or discontinued; regulatory requirements and uncertainties; dependence on third-party collaborators, laboratories, service providers, and data sources; intellectual property risks, including the ability to obtain, maintain, defend, and enforce patent and other proprietary rights; competitive developments; the availability, timing, and terms of strategic investments or other financing alternatives; the ability to enter into, maintain, or enforce collaborations, partnering arrangements, or commercial agreements on acceptable terms; and broader economic, market, geopolitical, or regulatory conditions.
Additional information about these and other risks and uncertainties is set out in the Company’s Annual Report on Form 20-F, as amended, for the fiscal year ended April 30, 2025, available on the Company’s SEDAR+ profile at www.sedarplus.ca and EDGAR profile at www.sec.gov/edgar.
Readers are cautioned not to place undue reliance on forward-looking statements. Except as required by applicable law, the Company undertakes no obligation to update or revise any forward-looking statements to reflect new information, future events, or otherwise.
This press release does not constitute an offer to sell or the solicitation of an offer to buy any securities.
View source version on businesswire.com: https://www.businesswire.com/news/home/20260126561251/en/
Investor Contact
Louie Toma, CPA, CFA
Managing Director, CoreIR
investors@mindwalkAI.com
Original: MindWalk Applies HYFT® Technology to Detect Functional Adjacency Linked to Portfolio Risk in AI-Designed Therapeutics