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throughline No. 222 October 12, 2026

Ascelia refuses new trial for Orviglance after FDA meeting

The public is reading the company's summary of the minutes, not the FDA complete response letter or the minutes themselves, which is the gap Commissioner Makary has described on camera as corporate spin.

The public is reading the company's summary of the minutes, not the FDA complete response letter or the minutes themselves, which is the gap Commissioner Makary has described on camera as corporate spin.

On October 11, 2026, Ascelia Pharma said FDA's Type A minutes still require a new clinical study for Orviglance, and the company said it will not run one.

Why it matters: People with severe kidney impairment who need liver imaging are waiting on whether a manganese contrast gets a U.S. approval path, and investors are waiting on a date the company has not set.

Date to watch: No next FDA date is posted. Ascelia scheduled a webcast for October 12, 2026, at 8:30 a.m. CEST, and named a cash runway into 2027.

Sources:

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