Intercept Announces FDA Acceptance of sNDA for Ocaliva
Dr. Reddy`s Laboratories` Generic Obeticholic Acid Receives Approval in the U.S.
It’s been an uphill battle for Intercept Pharmaceuticals in the three years since the FDA first nixed its attempt to bring Ocaliva to patients with nonalcoholic steatohepatitis (NASH)-related liver fibrosis.
Optimus' Generic Obeticholic Acid Receives Approval in the U.S.
Even after second application attempt, Intercept’s Ocaliva wasn’t the fatty liver disease breakthrough that the company had hoped it would be.
Company to discontinue all NASH-related investment and restructure the Company™s operations to strengthen its focus on rare and serious liver diseasesCompany anticipates achieving profitability in...
MSN's Generic Obeticholic Acid Receives Receives Approval in the U.S.
Apotex's Generic Obeticholic Acid Receives Receives Approval in the U.S.
Though the current conversation about brain-computer interfaces is largely dominated by two companies—Synchron, with a minimally invasive implant already in human trials, and Elon Musk’s Neuralink, which has faced a series of setbacks in its own race to the clinic—they’re not the only ones developing implants aimed at decoding neurological signals.
Intercept Announces FDA Advisory Committee Meeting Date for Obeticholic Acid as a Treatment for Pre-Cirrhotic Liver Fibrosis due to NASH