Key Insights

Highlights

Success Rate

100% trial completion (above average)

Published Results

22 trials with published results (47%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

0.0%

0 terminated out of 47 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

60%

28 trials in Phase 3/4

Results Transparency

52%

22 of 42 completed with results

Key Signals

22 with results100% success

Data Visualizations

Phase Distribution

41Total
P 1 (7)
P 2 (6)
P 3 (25)
P 4 (3)

Trial Status

Completed42
Unknown2
Recruiting1
Active Not Recruiting1
Not Yet Recruiting1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 42 completed trials

Clinical Trials (47)

Showing 20 of 20 trials
NCT07398755CompletedPrimary

Prospective, Non-interventional Study Assessing Periorbital Rejuvenation Procedure

NCT05248880Phase 3CompletedPrimary

A Study to Assess Adverse Events and Change in Disease Activity of Intramuscular AGN-151586 Injection in Toxin-Naïve Adult Participants With Glabellar Lines

NCT07374965CompletedPrimary

A Prospective, Non-Interventional, Single-Centre Study Assessing the Efficacy of a Holistic Upper Face Treatment With Botulinum Neurotoxin A

NCT07321834Phase 2Active Not RecruitingPrimary

A Study to Evaluate AI-09 In Participants With Glabellar Lines

NCT06834789Phase 1CompletedPrimary

A Study to Assess the Adverse Events of Intramuscular Injections of AGN-151586 and OnabotulinumtoxinA in Adult Participants for the Change of Glabellar Lines (GL)

NCT05100199Phase 2CompletedPrimary

A Study to the Assess the Change in Condition and Adverse Events of OnabotulinumtoxinA X Injection in Adult Participants With Glabellar Lines

NCT06246552Phase 2CompletedPrimary

Clinical Trial to Evaluate the Safety and Efficacy of JTM201 to Treat Moderate or Severe Glabellar Lines

NCT05089357CompletedPrimary

Non-interventional Study, Long Term Treatment on Glabellar Lines With Dysport® in Subjects of Chinese Origin

NCT05013424Phase 2CompletedPrimary

A Study of OnabotulinumtoxinA X Injection in Adult Participants With Glabellar Lines

NCT07013279Phase 3Not Yet RecruitingPrimary

Evaluate the Efficacy and Safety of DWP712 With Moderate to Severe Glabellar Lines

NCT06946160Phase 3CompletedPrimary

A Non-inferiority Clinical Trial to Compare Efficacy and Safety of Abobotulinumtoxin A (Espad Pharmed) Versus AbobotulinumtoxinA (Dysport®, Ipsen Co.) for Correction of Moderate to Severe Glabellar Lines

NCT06308198Phase 3CompletedPrimary

A Study to Evaluate AGN-151586 Intramuscular Injections in Adult Participants for Treatment of Glabellar Lines

NCT06205797Phase 3RecruitingPrimary

To Evaluate HU-045 in the Treatment of Glabellar Lines(Phase III)

NCT04157686Phase 3CompletedPrimary

MT10109L in the Long-term, Open-label Treatment of Glabellar Lines (GL) and Lateral Canthal Lines (LCL)

NCT05248893Phase 3CompletedPrimary

A Study to Assess Adverse Events of Intramuscular AGN-151586 Injection in Adult Participants With Glabellar Lines

NCT05248867Phase 3CompletedPrimary

A Study to Assess Adverse Events and Change in Disease Activity of Intramuscular AGN-151586 Injection in Adult Participants With Glabellar Lines

NCT06212960Phase 1CompletedPrimary

Evaluate the Safety and Explore the Efficacy of DWP712 With Moderate to Severe Glabellar Lines

NCT05801146Phase 3UnknownPrimary

Evaluate the Safety and Efficacy of HG102 as Compared to Botox® in Subject With Moderate to Severe Glabellar Lines

NCT05804656Phase 3CompletedPrimary

Efficacy and Safety of CKDB-501A in Subjects With Moderate-to-severe Glabellar Lines in Phase 3 Trial

NCT04096326Phase 2CompletedPrimary

AGN-151586 Dose-Ranging Study for Treatment of Glabellar Lines

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