Disc Medicine IRON
Disc Medicine announces positive APOLLO trial results
Item 7.01 Investor disclosure, Item 8.01 Other events
- Form
- 8-K
- Filed
- Importance
- Notable
- Accession
- 0001193125-26-424649
- Bitopertin met all primary and secondary endpoints in APOLLO Phase 3 trial
- Reduction in whole-blood PPIX by 41.4% vs. placebo (p<0.0001)
- Increase in average monthly light time without pain by 12.2 hours vs. placebo (p=0.0010)
- Bitopertin was generally well-tolerated with no Grade 3 TEAEs
Written from the 8-K on EDGAR. Check the filing before you rely on it.
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