Success Metrics

Clinical Success Rate
72.2%

Based on 13 completed trials

Completion Rate
72%(13/18)
Active Trials
1(5%)
Results Posted
131%(17 trials)
Terminated
5(25%)

Phase Distribution

Ph phase_1
5
25%
Ph phase_4
4
20%
Ph phase_3
10
50%
Ph phase_2
1
5%

Phase Distribution

5

Early Stage

1

Mid Stage

14

Late Stage

Phase Distribution20 total trials
Phase 1Safety & dosage
5(25.0%)
Phase 2Efficacy & side effects
1(5.0%)
Phase 3Large-scale testing
10(50.0%)
Phase 4Post-market surveillance
4(20.0%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

72.2%

13 of 18 finished

Non-Completion Rate

27.8%

5 ended early

Currently Active

1

trials recruiting

Total Trials

20

all time

Status Distribution
Active(1)
Completed(13)
Terminated(5)
Other(1)

Detailed Status

Completed13
Terminated5
Active, not recruiting1
unknown1

Development Timeline

Analytics

Development Status

Total Trials
20
Active
1
Success Rate
72.2%
Most Advanced
Phase 4

Trials by Phase

Phase 15 (25.0%)
Phase 21 (5.0%)
Phase 310 (50.0%)
Phase 44 (20.0%)

Trials by Status

active_not_recruiting15%
completed1365%
terminated525%
unknown15%

Recent Activity

Clinical Trials (20)

Showing 20 of 20 trials
NCT06742554Phase 4

Comparative Efficacy of Buprenorphine Transdermal Patch Versus Tramadol in Postoperative Analgesia for Shoulder Arthroscopy

Active Not Recruiting
NCT03975010Phase 1

Buprenorphine Transdermal Patches Pharmacokinetic Study

Unknown
NCT01999114Phase 1

The Effect of Buprenorphine Delivered by Buprenorphine Transdermal System (BTDS) at Doses up to 80 Micrograms/Hour (mcg/hr) and Naltrexone on Electrocardiogram (ECG) Intervals in Healthy Volunteers

Completed
NCT01961271Phase 4

Evaluation Of Efficacy And Safety Of Norspan In Moderate To Severe Pain Due To Osteoarthritis, Rheumatoid Arthritis, Joint/Muscle Pain

Completed
NCT02519387Phase 4

Efficacy and Safety of Buprenorphine Transdermal Patch in Non-cancer Pain of Moderate Intensity

Completed
NCT01259115Phase 1

Buprenorphine Accumulation and Description of Its Metabolites During Co-Medication of Buprenorphine Transdermal System (BTDS) and Ketoconazole

Completed
NCT01276431Phase 4

Norspan Efficacy and Safety Among Elderly Subjects

Completed
NCT01151098Phase 3

Safety of Buprenorphine Transdermal Systems in Subjects With Chronic Nonmalignant Pain - a 28-week Extension Study

Completed
NCT00312195Phase 3

Safety and Efficacy of Buprenorphine Transdermal System (BTDS) in Subjects With Chronic Nonmalignant Pain

Completed
NCT01135524Phase 3

Safety of Buprenorphine Transdermal Patch (BTDS) in Osteoarthritis Pain: a 52-Week Extension Phase

Terminated
NCT01125917Phase 3

Safety of BTDS in Subjects With Low Back Pain: A 52-Week Extension Phase of BUP3015

Terminated
NCT00315445Phase 3

The Safety and Efficacy of the Buprenorphine Transdermal System (BTDS) in Subjects With Chronic Back Pain.

Completed
NCT01148537Phase 1

The Effect of Buprenorphine Delivered by Buprenorphine Transdermal System (BTDS) on QT Intervals in Healthy Volunteers

Completed
NCT00320801Phase 3

Buprenorphine Transdermal Patches (BTDS) in Subjects With Osteoarthritis Pain. Includes a 52-week Extension Phase.

Terminated
NCT00312572Phase 3

Safety and Efficacy of Dose Conversion From Vicodin® to Buprenorphine Transdermal System (Butrans™) in Subjects With OA Pain

Completed
NCT00313846Phase 3

Safety and Efficacy of Buprenorphine Transdermal System in Subjects With Moderate to Severe Osteoarthritis of Hip or Knee

Completed
NCT00315458Phase 3

Buprenorphine Transdermal Patch in Subjects With Osteoarthritis Pain Requiring Opioids. Includes a 52-Week Safety Extension.

Terminated
NCT00403234Phase 2

Safety of Buprenorphine Transdermal System (BTDS) in Subjects With Acute Postoperative Pain After Total Knee Replacement

Terminated
NCT01141283Phase 3

Safety of BTDS in Subjects With Osteoarthritic (OA) Pain of Hip or Knee: A 6-Month Open-label Extension Phase

Completed
NCT01259102Phase 1

Examine Plasma Concentrations of Buprenorphine Following Reapplication of Buprenorphine Transdermal System (BTDS) After Variable Application Site Rest Periods

Completed

All 20 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
20