Celcuity Inc., a clinical-stage biotech, reported a net loss of $177.0 million for FY 2025, up from $111.8 million in FY 2024, driven by elevated operating expenses of $172.2 million versus $113.3 million prior year.
52W $8.21 – $117.25
Celcuity Inc., a clinical-stage biotech, reported a net loss of $177.0 million for FY 2025, up from $111.8 million in FY 2024, driven by elevated operating expenses of $172.2 million versus $113.3 million prior year.
Celcuity Inc., a clinical-stage biotech, reported a net loss of $177.0 million for FY 2025, up from $111.8 million in FY 2024, driven by elevated operating expenses of $172.2 million versus $113.3 million prior year. Research and development costs surged to $145.0 million from $104.2 million, reflecting accelerated clinical trials including VIKTORIA-1 (completed enrollment, topline data reported for PIK3CA WT...
Celcuity Inc., a clinical stage biotechnology company, focuses on the development of molecularly targeted therapies for cancer patients in the United States. The company's CELsignia diagnostic platform uses a patient's living tumor cells to identify the specific abnormal cellular process driving a patient's cancer and the related targeted therapy for the treatment. Its drug candidate includes Gedatolisib, which selectively targets various class I isoforms of PI3K and mammalian target of rapamycin and focus on the treatment of patients with hormone receptor positive, HER2-negative, and advanced or metastatic breast cancer. The company is also developing CELsignia MP test, a qualitative laboratory developed test that measures HER2, c-Met, and PI3K signaling activity in breast and ovarian tumor cells. It had a license agreement with Pfizer, Inc. for the development and commercialization rights to Gedatolisib. Celcuity Inc. was founded in 2011 and is headquartered in Minneapolis, Minnesota.