- Phase 3 open-label, single-arm study conducted in Japan by BridgeBio licensing partner Alexion, AstraZeneca Rare Disease showed consistency with global ATTRibute-CM Phase III trial
- No mortality was reported over the 30 month acoramidis treatment period
- Acoramidis was well-tolerated, with no safety signals of potential clinical concern identified
- These results support local regulatory submission in Japan
- The findings from this study build upon positive results from BridgeBio’s global ATTRibute-CM Phase 3 trial, where the primary endpoint was met (Win Ratio of 1.8) with a highly statistically significant p-value (p

