Pharvaris Announces Statistically Significant And Clinically Meaningful Topline Results From Its CHAPTER-3 Pivotal Phase 3 Study Evaluating Deucrictibant Extended-Release Tablet For Prevention Of HAE Attacks; Primary Endpoint And All Secondary Efficacy Endpoints Were Met With Statistical Significance
Primary endpoint met: 83% attack rate reduction versus placebo (p<0.0001) in the first and only prophylaxis Phase 3 study in all three types of HAE87% attack rate reduction versus placebo observed in people with HAE
Pharvaris's medicine worked really well in testing—it stopped way more attacks than a fake medicine, which is what doctors hoped would happen. When a company proves their medicine actually works, that's important information about whether the business might succeed.
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Source: Benzinga · Read the original report at the publisher. Headline and figures shown for context; data may be delayed.
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