Clinical Trial

Study to Assess KN3835 in the Treatment of Flexible/Semi-Flexible Hammertoe (HMT)

Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
The primary purpose of this study is to assess the efficacy, safety, and tolerability of KN3835 compared to placebo in the treatment of flexible/semi-flexible HMT.
Trial Details
NCT Number NCT07759362
Lead Sponsor Endo USA Inc., a Keenova Therapeutics Company
Conditions Flexible Hammertoe, Semi-flexible Hammertoe
Enrollment 554 participants
Start Date 2026-08
Primary Completion 2027-12 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2026-08-12