Omeros Corporation Announces Upcoming Presentations at ASH Annual Meeting
2024年12月2日 - 10:45PM
ビジネスワイヤ(英語)
-- Presentations Highlight Progress in
Late-Stage Development of Lead MASP-3 Inhibitor Zaltenibart --
Omeros Corporation (Nasdaq: OMER) today announced that two
abstracts directed to zaltenibart (OMS906), Omeros’ investigational
inhibitor of MASP-3, the key activator of the alternative pathway
of complement, will be presented at the 66th Annual Meeting of the
American Society of Hematology (ASH), to be held December 7-10,
2024 in San Diego. The zaltenibart abstracts are directed to the
treatment of paroxysmal nocturnal hemoglobinuria (PNH), a rare,
life-threatening hematological disorder. Enrollment for the
zaltenibart Phase 3 clinical trials in PNH is expected to open in
early 2025.
Both abstracts are available on the ASH website at
www.hematology.org. Details of the congress presentations and
direct links to the abstracts are found below.
Monotherapy Treatment with Zaltenibart
(OMS906), an Alternative Pathway Masp-3 Inhibitor, Improved Key
Hematologic Parameters in Patients with PNH with a Suboptimal
Response to Ravulizumab: Interim Results from a Phase 2
Proof-of-Concept Study Abstract Number / Link: 4072 Session:
508. Bone Marrow Failure: Acquired: Poster III Presentation Time:
Monday, December 9, 2024, 6:00 PM-8:00 PM Location: San Diego
Convention Center, Halls G-H Presenting Author: Morag Griffin,
MBChB, MRCP
Population
Pharmacokinetics/Pharmacodynamics and Clinical Pharmacology of
Zaltenibart (OMS906) in Healthy Subjects and Patients with PNH
Abstract Number / Link: 4081 Session: 508. Bone Marrow Failure:
Acquired: Poster III Presentation Time: Monday, December 9, 2024,
6:00 PM-8:00 PM Location: San Diego Convention Center, Halls G-H
Presenting Author: William Pullman, BMedSc, MBBS, PhD, FRACP
The presentation materials associated with each abstract will be
made available on Omeros’ website at www.omeros.com following the
congress presentations.
About OMS906
OMS906 is an investigational human monoclonal antibody targeting
mannan-binding lectin-associated serine protease-3 (MASP-3), the
key and most proximal activator of the complement system’s
alternative pathway. The complement system is a critical part of
innate immunity and plays a central role in host homeostasis and
defense against pathogens. Responsible for the conversion of
pro-complement factor D to complement factor D, MASP-3 is believed
to be the premier target in the alternative pathway – it has the
lowest native circulating level and low relative clearance compared
to the other alternative pathway proteins and, unlike C5 and C3
blockers, MASP-3 inhibition leaves intact the lytic arm of the
classical pathway, important for fighting infection. Also, unlike
other components of the alternative pathway, MASP-3 is believed not
to be an acute phase reactant, which could provide a significant
advantage to MASP-3 inhibitors, like OMS906, over other alternative
pathway inhibitors. MASP-3 inhibitors are thought to have
preventive or therapeutic effects across a broad range of diseases
including paroxysmal nocturnal hemoglobinuria (PNH), hemolytic
uremic syndrome (HUS), atypical HUS, traumatic brain injury,
arthritis, geographic atrophy or “dry” macular degeneration,
ischemia-reperfusion injury, transplant-related complications and
other immune-related disorders.
About Omeros Corporation
Omeros is an innovative biopharmaceutical company committed to
discovering, developing and commercializing first-in-class
small-molecule and protein therapeutics for large-market and orphan
indications targeting immunologic disorders, including
complement-mediated diseases and cancers, as well as addictive and
compulsive disorders. Omeros’ lead MASP-2 inhibitor narsoplimab
targets the lectin pathway of complement and is the subject of a
biologics license application pending before FDA for the treatment
of hematopoietic stem cell transplant-associated thrombotic
microangiopathy. Omeros’ long-acting MASP-2 inhibitor OMS1029 has
successfully completed Phase 1 single- and multiple-ascending dose
clinical studies. OMS906, Omeros’ inhibitor of MASP-3, the key
activator of the alternative pathway of complement, is advancing
toward Phase 3 clinical trials for paroxysmal nocturnal
hemoglobinuria and complement 3 glomerulopathy. Funded by the
National Institute on Drug Abuse, Omeros’ lead phosphodiesterase 7
inhibitor OMS527 is in clinical development for the treatment of
cocaine use disorder. Omeros also is advancing a broad portfolio of
five novel cellular and molecular immuno-oncology programs. For
more information about Omeros and its programs, visit
www.omeros.com.
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version on businesswire.com: https://www.businesswire.com/news/home/20241202587501/en/
Jennifer Cook Williams Cook Williams Communications, Inc.
Investor and Media Relations IR@omeros.com
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