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Celcuity Shares Fall Despite Strong Phase 3 Breast Cancer Trial Data (CELC)June 2, 2026 9:40 AM
IH Market News Celcuity Inc. (NASDAQ:CELC) shares dropped 15% on Tuesday even after the company released detailed positive efficacy and safety findings from the PIK3CA-mutant cohort of its Phase 3 VIKTORIA-1 study evaluating gedatolisib in patients with hormone receptor-positive, HER2-negative, PIK3CA-mutated advanced or metastatic breast cancer. The decline came despite data showing significant improvements in progression-free survival and disease control compared with current treatment options. Gedatolisib Triplet Therapy Delivers Strong Efficacy Results According to the study results, treatment with gedatolisib in combination with fulvestrant and palbociclib reduced the risk of disease progression or death by 50% compared with alpelisib plus fulvestrant. Patients receiving the gedatolisib-based triplet therapy achieved a median progression-free survival of 11.1 months, nearly double the 5.6 months reported in the comparator group. The findings suggest the regimen may offer a meaningful improvement for patients with this specific breast cancer subtype. Doublet Therapy Also Shows Significant Benefit The study also evaluated gedatolisib combined with fulvestrant without palbociclib. Results showed that the doublet regimen lowered the risk of disease progression or death by 49% compared with alpelisib plus fulvestrant. Median progression-free survival reached 11.3 months in the gedatolisib-plus-fulvestrant group, compared with 5.6 months for patients treated with alpelisib and fulvestrant. The consistency of the results across both treatment approaches reinforced confidence in the drug’s therapeutic potential. Response Rates and Durability Remain Encouraging Beyond progression-free survival, the trial also demonstrated strong tumor response outcomes. The gedatolisib triplet regimen produced an objective response rate of 48.9%, with a median duration of response of 15.7 months. Meanwhile, the gedatolisib doublet achieved a 35.7% objective response rate and an even longer median duration of response of 24.2 months. These results indicate that many patients experienced sustained clinical benefit from treatment. Favorable Safety Profile Observed Investigators reported that the gedatolisib-based regimens were generally well tolerated. Most treatment-related adverse events were low grade, and discontinuation rates due to treatment-related side effects remained comparatively low. Treatment-related adverse events resulted in discontinuation for 2.6% of patients receiving the gedatolisib triplet, 3.8% of patients receiving the gedatolisib doublet, and 7.1% of patients treated with alpelisib plus fulvestrant. The lower discontinuation rates may strengthen the drug’s competitive position if approved. Regulatory Submissions Planned Celcuity said it plans to submit the new clinical data to the U.S. Food and Drug Administration as part of a supplemental New Drug Application, while also pursuing submissions to regulatory agencies in other markets. The company is already advancing regulatory efforts for gedatolisib in another breast cancer indication. The FDA has granted Priority Review status to Celcuity’s New Drug Application for gedatolisib in patients with HR-positive, HER2-negative, PIK3CA wild-type advanced breast cancer. The application carries a Prescription Drug User Fee Act (PDUFA) target decision date of July 17, 2026. Investors Focus on Future Commercial Prospects Although the latest data demonstrated strong efficacy and a favorable safety profile, investors appeared to take profits following recent gains or reassess expectations around the commercial opportunity and regulatory pathway. Nevertheless, the VIKTORIA-1 results further strengthen the clinical case for gedatolisib and provide additional evidence supporting its potential role in the treatment of advanced breast cancer. With an FDA decision approaching and further regulatory submissions planned, Celcuity remains focused on advancing the therapy toward commercialization and expanding its presence in the oncology market. Celcuity stock price Original: Celcuity Shares Fall Despite Strong Phase 3 Breast Cancer Trial Data (CELC)
INV4
11月前
Celcuity Announces Clinically Meaningful Improvement in Both Progression-Free Survival (“PFS”) Primary Endpoints from PIK3CA Wild-Type Cohort of Phase 3 VIKTORIA-1 Trial
July 28, 2025
Celcuity Inc. (Nasdaq: CELC), a clinical-stage biotechnology company pursuing development of targeted therapies for oncology, today announced positive topline results from the PIK3CA wild-type cohort of the Phase 3 VIKTORIA-1 clinical trial evaluating gedatolisib plus fulvestrant with and without palbociclib versus fulvestrant in adults with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, PIK3CA wild-type, locally advanced or metastatic breast cancer, following progression on, or after, treatment with a CDK4/6 inhibitor and an aromatase inhibitor.
In the trial, the gedatolisib triplet demonstrated a statistically significant and clinically meaningful improvement in PFS among patients, reducing the risk of disease progression or death by 76% compared to fulvestrant (based on a hazard ratio [HR] of 0.24, 95% confidence interval [CI] 0.17-0.35; p<0.0001). The mPFS, as assessed by blinded independent central review (“BICR”), was 9.3 months with the gedatolisib triplet versus 2.0 months with fulvestrant, an incremental improvement of 7.3 months.
The gedatolisib doublet also demonstrated a statistically significant and clinically meaningful improvement in PFS among patients, reducing the risk of disease progression or death by 67% compared to fulvestrant (HR of 0.33, 95% CI 0.24-0.48; p<0.0001). The mPFS, as assessed by BICR, was 7.4 months with the gedatolisib doublet versus 2.0 months with fulvestrant, an incremental improvement of 5.4 months.
The topline efficacy data from the VIKTORIA-1 PIK3CA wild-type cohort established several new milestones in the history of drug development for HR+/HER2- advanced breast cancer:
• The hazard ratios for the gedatolisib triplet and doublet are more favorable than have ever been reported by any Phase 3 trial for patients with HR+/HER2- ABC.
• The 7.3- and 5.4-months incremental improvements in median PFS for the gedatolisib triplet and gedatolisib doublet over fulvestrant, respectively, are higher than have ever been reported by any Phase 3 trial for patients with HR+/HER2- ABC receiving at least their second line of therapy.
• Gedatolisib is the first inhibitor targeting the PI3K/AKT/mTOR pathway to demonstrate positive Phase 3 results in patients with HR+/HER2-/PIK3CA wild-type ABC whose disease progressed on or after treatment with a CDK4/6 inhibitor.
Sara Hurvitz, MD, Senior Vice President, Clinical Research Division, Fred Hutchinson Cancer Center, Professor and Head, Division of Hematology and Oncology, University of Washington, Department of Medicine and co-principal investigator for the trial said: “Patients with HR-positive, HER2-negative, PIK3CA wild-type advanced breast cancer whose disease has progressed while on, or after, treatment with a CDK4/6 inhibitor typically derive limited benefit from subsequent endocrine-based therapy. The topline data for both gedatolisib regimens from VIKTORIA-1 are potentially practice-changing. To my knowledge, we have not seen Phase 3 results in patients with HR-positive, HER2-negative advanced breast cancer before where there was a quadrupling of the likelihood of survival without disease progression relative to the study control.”
Treatment discontinuation due to a treatment-related adverse event for the gedatolisib triplet and gedatolisib doublet was lower than was observed in Arm D of the Phase 1b trial in patients with ABC, and lower than observed in any Phase 3 trials for currently approved drug combinations in HR+/HER2- ABC. Additionally, the gedatolisib triplet and gedatolisib doublet were better tolerated than was observed in the Phase 1b trial in patients with ABC, including lower rates of hyperglycemia and stomatitis.
Igor Gorbatchevsky, MD, Chief Medical Officer of Celcuity said: “The topline data from VIKTORIA-1 demonstrate the potential for gedatolisib to become a transformative new medicine for the treatment of patients with HR-positive, HER2-negative, PIK3CA wild-type advanced breast cancer whose disease progressed on or after treatment with CDK4/6 inhibitors. The 7.3 and 5.4-months incremental improvement in median PFS relative to fulvestrant for the gedatolisib regimens are potentially paradigm shifting results. We are also very excited that treatment with gedatolisib combined with fulvestrant with or without palbociclib was well-tolerated by the VIKTORIA-1 patients and that only a few patients discontinued treatment due to an adverse event.”
Brian Sullivan, Chairman, Chief Executive Officer and co-founder of Celcuity said, “The efficacy improvement relative to the control that each of the gedatolisib regimens demonstrated was historic for this patient population. We are excited about the potential opportunity to provide a breakthrough therapeutic option for patients with HR-positive, HER2-negative, PIK3CA wild-type advanced breast cancer.”
Full data from the PIK3CA wild-type cohort of the VIKTORIA-1 clinical trial will be presented at an upcoming medical conference later this year. Celcuity expects to submit a New Drug Application for gedatolisib to the U.S. Food and Drug Administration in the fourth quarter of 2025. Topline data for the VIKTORIA-1 PIK3CA mutation cohort is expected by the end of 2025.
Webcast and Conference Call Information
The Celcuity management team will host a webcast/conference call on Monday, July 28, 2025, at 8:00 a.m. ET to discuss the topline results from the Phase 3 VIKTORIA-1 trial. Those who would like to participate may access the live webcast here, or register in advance for the teleconference here. A replay of the webcast will be available on the Celcuity website following the live event.
Notes
HR+/HER2- Breast cancer
Breast cancer is the second most common cancer and one of the leading causes of cancer-related deaths worldwide.1 More than two million breast cancer cases were diagnosed globally in 2022.1 While survival rates are high for those diagnosed with early breast cancer, only approximately 30% of patients who are diagnosed with or who progress to metastatic disease are expected to live five years after their diagnosis.2 HR+/HER2- breast cancer is the most common subtype of breast cancer, accounting for approximately 70% of all breast cancers.2
Three interconnected signaling pathways, estrogen, cyclin D1-CDK4/6, and PI3K/AKT/mTOR (PAM), are primary oncogenic drivers of HR+, HER2- breast cancer.3 Therapies inhibiting these pathways are approved and used in various combinations for advanced breast cancer. Currently approved inhibitors of the PAM pathway for breast cancer target a single PAM pathway component, such as PI3Ka, AKT, or mTORC1.4,5,6,7 However, resistance to CDK4/6 inhibitors and current endocrine therapies develops in many patients with advanced disease.8 Survival rates are low with 30% of patients anticipated to live beyond five years after diagnosis.2 Optimizing the inhibition of the PAM pathway is an active area of focus for breast cancer research.
VIKTORIA-1
VIKTORIA-1 is a Phase 3 open-label, randomized clinical trial to evaluate the efficacy and safety of gedatolisib in combination with fulvestrant with or without palbociclib in adults with HR+/HER2- ABC whose disease progressed on or after prior CDK4/6 therapy in combination with an aromatase inhibitor. The clinical trial is enrolling subjects regardless of PIK3CA status while enabling separate evaluation of subjects according to their PIK3CA status. Subjects who meet eligibility criteria and do not have confirmed PI3KCA mutations (WT) were randomly assigned (1:1:1) to receive a regimen of either gedatolisib, palbociclib, and fulvestrant, gedatolisib and fulvestrant, or fulvestrant. Subjects who meet eligibility criteria and have confirmed PI3KCA mutations (MT) are randomly assigned (3:3:1) to receive a regimen of either the gedatolisib triplet, alpelisib and fulvestrant, or the gedatolisib doublet.
Gedatolisib
Gedatolisib is an investigational, multi-target PAM inhibitor that potently targets all four class I PI3K isoforms, mTORC1, and mTORC2 to induce comprehensive blockade of the PAM pathway.9,10,11 As a multi-target PAM inhibitor, gedatolisib’s mechanism of action is highly differentiated from currently approved single-target inhibitors of the PAM pathway.11 Inhibition of only a single PAM component gives tumors an escape mechanism through cross-activation of the uninhibited targets. Gedatolisib’s comprehensive PAM pathway inhibition ensures full suppression of PAM activity by eliminating adaptive resistance cross-activation that occurs with single-target inhibitors. Unlike single-target inhibitors of the PAM pathway, gedatolisib has demonstrated equal potency and comparable cytotoxicity in PIK3CA-mutant and -wild-type breast tumor cells in nonclinical studies and early clinical data.11,12
About Celcuity
Celcuity is a clinical-stage biotechnology company pursuing development of targeted therapies for treatment of multiple solid tumor indications. The company's lead therapeutic candidate is gedatolisib, a potent, pan-PI3K and mTORC1/2 inhibitor that comprehensively blockades the PAM pathway. Its mechanism of action and pharmacokinetic properties are differentiated from other currently approved and investigational therapies that target PI3Ka, AKT, or mTORC1 alone or together. A Phase 3 clinical trial, VIKTORIA-1, evaluating gedatolisib in combination with fulvestrant with or without palbociclib in patients with HR+/HER2- advanced breast cancer is currently enrolling patients. A Phase 1/2 clinical trial, CELC-G-201, evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is ongoing. A Phase 3 clinical trial, VIKTORIA-2, evaluating gedatolisib plus a CDK4/6 inhibitor and fulvestrant as first-line treatment for patients with HR+/HER2- advanced breast cancer is currently enrolling patients. More detailed information about Celcuity’s active clinical trials can be found at ClinicalTrials.gov. Celcuity is headquartered in Minneapolis. Further information about Celcuity can be found at www.celcuity.com. Follow us on LinkedIn and X.
https://ih.advfn.com/stock-market/NASDAQ/celcuity-CELC/stock-news/96505671/celcuity-announces-clinically-meaningful-improveme
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