A follow-up study to assess the long-term safety of intra-articular (IA) administration of UBX0101 in patients with painful knee osteoarthritis (OA).
This is a blinded, multi-center study to provide approximately 1 additional year of follow-up for patients with knee OA who participated in a randomized placebo-controlled study of IA UBX0101. No intervention is planned and patients will have 4 scheduled visits to collect follow-up assessments. The primary objective is to evaluate long-term safety and tolerability of IA administration of UBX0101 in patients with painful knee OA.
Study Type
OBSERVATIONAL
Enrollment
161
This is an observational study. No intervention is administered.
Coastal Clinical Research, LLC.
Mobile, Alabama, United States
Fiel Family and Sports Medicine
Tempe, Arizona, United States
Incidence of adverse events up to 1 additional year of follow up.
Time frame: 52 weeks
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