Phase 2Completed

A Study to Assess the Safety and Efficacy of a Single Dose of UBX0101 in Patients With Osteoarthritis of the Knee

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Single-Dose Study of UBX0101 in Moderate to Severe, Painful Osteoarthritis of the Knee

Sponsor
Unity Biotechnology, Inc. (Industry)
Enrolment
183 enrolled
Conditions
Osteoarthritis, Knee
Interventions
UBX0101; Placebo
Ages
adults, older adults
Registry
NCT04129944

From the registry

A study to assess efficacy, safety, and tolerability of a single-dose intra-articular administration of UBX0101 in patients with moderate to severe painful knee osteoarthritis (OA).

Primary outcomes

  • Change From Baseline to Week 12 of the Western Ontario and McMaster Universities Osteoarthritis Index Pain Subscale (WOMAC-A) Score in Patients Receiving a Single Dose of UBX0101 Versus Those Receiving Placebo
Full record on ClinicalTrials.gov