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Corcept Therapeutics is conducting a Phase 2 study to evaluate the safety and efficacy of dazucorilant in treating Amyotrophic Lateral Sclerosis (ALS). The study aims to determine the drug's effectiveness in slowing ALS progression, with two doses of 300 mg and 150 mg compared to a placebo. Successful results could significantly impact Corcept Therapeutics' stock and position in the ALS treatment space.
Corcept Therapeutics Incorporated (CORT) has been actively pursuing innovative treatments for various diseases, including Amyotrophic Lateral Sclerosis (ALS). The company recently announced an update on its Phase 2 clinical study evaluating the safety and efficacy of dazucorilant in treating ALS. The study, titled 'A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Evaluating Safety and Efficacy of CORT113176 (Dazucorilant) in Patients With Amyotrophic Lateral Sclerosis (DAZALS)', aims to assess the drug's effectiveness in slowing ALS progression [2].
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