drugset / Trial / NCT05085561

The Symptomatic Cerebral Cavernous Malformation Trial of REC-994

NCT05085561 ↗

Phase 2 Completed 62 enrolled Recursion Pharmaceuticals Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a two-part, multi-center, randomized, double-blind, placebo-controlled study to investigate the safety, efficacy and pharmacokinetics of REC-994 (200 mg and 400 mg) compared to placebo in participants with symptomatic cerebral cavernous malformation (CCM).

Timeline

Start
2022-03-17
Primary completion
2025-06-30
Completion
2025-06-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator REC-994 Unknown 200 mg —
Comparator REC-994 Unknown 400 mg —