drugset / Trial / NCT07397468

To studyJUV-161 Administered to Healthy Volunteers Undergoing Unilateral Lower Limb Immobilization (ULLI)

NCT07397468 ↗

Phase 1/2 Recruiting 36 enrolled Juvena Therapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a double-blind, placebo-controlled, randomized study of 96 days total duration to assess the effect of JUV-161 on muscle disuse atrophy. This will be a multicenter study in New Zealand and will include up to 40 healthy volunteers aged between 40 to 65 years of age. Following the screening period, subjects will be randomized to receive either weekly subcutaneous (SC) injections of one of two doses of JUV-161 or matching placebo for a period of approximately 6 weeks.

Timeline

Start
2026-02-28
Primary completion
2026-07-31
Completion
2026-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject JUV-161 Unknown 5 mg/kg Subcutaneous
Subject JUV-161 Unknown 10 mg/kg Subcutaneous

Indications

No indication recorded.