drugset / Trial / NCT05130866

Efficacy and Safety of REC-2282 in Patients With Progressive Neurofibromatosis Type 2 (NF2) Mutated Meningiomas

NCT05130866

Phase 2/3 Terminated 25 enrolled Recursion Pharmaceuticals Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a two-staged, Phase 2/3, randomized, multi-center study to investigate the efficacy and safety of REC-2282 in participants with progressive NF2 mutated meningiomas.

Timeline

Start
2022-06-20
Primary completion
2025-08-18
Completion
2025-08-18

Drugs

EvaluationDrugModalityDoseRoute
Subject AR-42 Small molecule 40 mg Oral
Subject AR-42 Small molecule 60 mg Oral