Safety of Buprenorphine Transdermal Patch (BTDS) in Osteoarthritis Pain: a 52-Week Extension Phase
A Randomized, Double-blind, Multicenter, Active Comparator Study to Determine the Efficacy and Safety of BTDS 20 or OxyIR® Versus BTDS 5 in Subjects With Moderate to Severe Osteoarthritis (OA) Pain: A 52-Week Extension Phase
Sponsor: Purdue Pharma LP
Terminated
This study was terminated early for administrative reasons.
Other terminated trials from Purdue Pharma LP
- Attention Deficit/Hyperactivity Disorder · Phase PHASE4 · Apr 2022
- Attention-Deficit/Hyperactivity Disorder · Phase PHASE4 · Jan 2022
- Osteoarthritis Pain of the Knee · Phase PHASE2 · Nov 2016
- Postsurgical Pain Due to Third Molar Extraction · Phase PHASE2 · Nov 2013
- Back Pain Lower Back Chronic · Phase PHASE3 · Jan 2008
This PHASE3 trial investigates Osteoarthritis and is currently terminated or withdrawn. Purdue Pharma LP leads this study, which shows 8 recorded versions since 2004 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
8 versions recorded-
Sep 2025 — Present [monthly]
Terminated PHASE3
-
Sep 2024 — Sep 2025 [monthly]
Terminated PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Terminated PHASE3
-
Dec 2021 — Jul 2024 [monthly]
Terminated PHASE3
-
Jan 2021 — Dec 2021 [monthly]
Terminated PHASE3
▶ Show 3 earlier versions
-
Jun 2018 — Jan 2021 [monthly]
Terminated PHASE3
-
Feb 2017 — Jun 2018 [monthly]
Terminated PHASE3
-
Jan 2017 — Feb 2017 [monthly]
Terminated PHASE3
First recorded
Apr 2004
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Purdue Pharma LP
For direct contact, visit the study record on ClinicalTrials.gov .