drugset / Trial / NCT06619847

A Study Evaluating Efficacy and Safety of VX-993 for Acute Pain After a Bunionectomy

NCT06619847 ↗

Phase 2 Completed 367 enrolled Vertex Pharmaceuticals Incorporated
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy, safety, tolerability and pharmacokinetics of VX-993 in treating acute pain after a bunionectomy.

Timeline

Start
2024-10-29
Primary completion
2025-05-27
Completion
2025-05-27

Outcome

Missed primary endpoint

release “Treatment with the selective NaV1.8 pain signal inhibitor VX-993 after bunionectomy surgery did not meet the primary endpoint” vrtx.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Acetaminophen Small molecule — Oral
Comparator Hydrocodone Unknown — Oral
Subject VX-993 Unknown — Oral

Indications

No indication recorded.