Disc Medicine's Bitopertin Meets All Primary and Secondary Endpoints in Phase 3 EPP Trial

Bitget2026/10/19 11:13

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Disc Medicine on Oct. 19, 2026, reported bitopertin met all primary and secondary endpoints in the Phase 3 APOLLO trial.
Results in erythropoietic protoporphyria showed increased pain-free time in light, fewer phototoxic reactions and improved quality of life versus placebo.
Bitopertin was generally well tolerated, with no new safety signals; dizziness was the most common treatment-related adverse event.
An FDA application resubmission is planned by year-end 2026, with a decision anticipated by mid-2027.
Topline results were announced; more detailed findings will be presented at a future medical conference.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Disc Medicine Inc. i published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202610190700PRIMZONEFULLFEED9848066) on October 19, 2026, and is solely responsible for the information contained therein.

Disclaimer: The content of this article solely reflects the author's opinion and does not represent the platform in any capacity. This article is not intended to serve as a reference for making investment decisions.

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Disc Medicine's Bitopertin Meets All Primary and Secondary Endpoints in Phase 3 EPP Trial

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