drugset / Trial / NCT05211986

Safety and Tolerability of IMM01-STEM in Patients With Muscle Atrophy Related to Knee Osteoarthritis.

NCT05211986 ↗

Phase 1/2 Recruiting 28 enrolled Immunis, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

An open-label dose escalation study to assess the safety and tolerability of IMM01-STEM in participants with muscle atrophy related to knee osteoarthritis

Timeline

Start
2022-09-13
Primary completion
2026-03-30
Completion
2026-06-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator IMM01-STEM Unknown 225 ug Intramuscular
Comparator IMM01-STEM Unknown 450 ug Intramuscular
Comparator IMM01-STEM Unknown 900 ug Intramuscular
Comparator IMM01-STEM Unknown 2000 ug Intramuscular

Indications