Corcept Therapeutics

Ovarian cancer
#Corcept Therapeutics #Oncology #Ovarian cancer #Phase III trial

Combo treatment new SOC in platinum-resistant ovarian cancer

Corcept Therapeutics has shared final overall survival data from its pivotal Phase III ROSELLA trial of Lifyorli (relacorilant) combined with the chemotherapeutic agent nab-paclitaxel in patients with platinum-resistant ovarian cancer.  The results were shared in a late-breaking oral presentation at the Society of Gynecologic Oncology (SGO) 2026… Read More

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#AI / data analytics / healthtech / informatics #ALS #Alzheimer's #Axol Bioscience #Biologics #Centessa Pharmaceuticals #Corcept Therapeutics #Denali Therapeutics #Eli Lilly #FDA #Hunter Syndrome #LifeArc #Mergers and acquisitions #MND #Ovarian cancer #Stanford University

DDW Highlights: 7 April 2026

The latest episode of the DDW Highlights Podcast is now available to listen to below. DDW’s Bruno Quinney narrates five key stories of the previous week to keep DDW subscribers up-to-date on the latest industry news. Last week, there were crucial developments in neuroscience drug discovery. Elsewhere, a new treatment for… Read More

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Ovarian cancer
#Corcept Therapeutics #FDA #Oncology #Ovarian cancer

Platinum-resistant ovarian cancer drug gets FDA green light

The US Food and Drug Administration (FDA) has approved Lifyorli (relacorilant) in combination with nab-paclitaxel for the treatment of adults with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer.  It is approved in patients who have received one to three prior systemic treatment regimens, at least… Read More

#News #Regulatory

Ovarian cancer cells
#Corcept Therapeutics #Oncology #Ovarian cancer #Phase III trial

Ovarian cancer drug reduces risk of death by 35%

Corcept Therapeutics has announced that ROSELLA, the company’s Phase III trial of relacorilant plus nab-paclitaxel to treat patients with platinum-resistant ovarian cancer, met its overall survival primary endpoint.  In ROSELLA, patients treated with relacorilant in addition to nab-paclitaxel chemotherapy experienced a 35% reduction in the risk of… Read More

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#Corcept Therapeutics #FDA #Hypertension

Regulator requests “additional evidence” for hypertension drug 

The US Food and Drug Administration (FDA) has issued a Complete Response Letter (CRL) to Corcept Therapeutics regarding the New Drug Application (NDA) for relacorilant as a treatment for patients with hypertension secondary to hypercortisolism.  While the FDA acknowledged that Corcept’s pivotal GRACE trial met its primary… Read More

#News #Regulatory