Key Insights

Highlights

Success Rate

100% trial completion (above average)

Published Results

23 trials with published results (46%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

0.0%

0 terminated out of 50 trials

Success Rate

100.0%

+13.4% vs benchmark

Late-Stage Pipeline

60%

30 trials in Phase 3/4

Results Transparency

53%

23 of 43 completed with results

Key Signals

23 with results100% success

Data Visualizations

Phase Distribution

44Total
P 1 (8)
P 2 (6)
P 3 (27)
P 4 (3)

Trial Status

Completed43
Not Yet Recruiting2
Recruiting2
Unknown2
Active Not Recruiting1

Trial Success Rate

100.0%

Benchmark: 86.6%

Based on 43 completed trials

Clinical Trials (50)

Showing 20 of 20 trials
NCT05248893Phase 3CompletedPrimary

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

NCT07756580Phase 1RecruitingPrimary

A Study to Evaluate Sequential Administration of Injections of AGN-151586 Followed by BOTOX in Adult Participants for Treatment of Glabellar Lines

NCT07783763Phase 3Not Yet RecruitingPrimary

Study of DWP450 in Japanese Subjects With Glabellar Lines

NCT06308198Phase 3CompletedPrimary

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

NCT05496335Phase 1CompletedPrimary

A Study to Evaluate Sequential Administration of AGN-151586 and OnabotulinumtoxinA (BOTOX) Injections in Adult Participants for Treatment of Glabellar Lines

NCT07622004Phase 3CompletedPrimary

Evaluate the Efficacy and Safety of INI101 Compared to BOTOX® in Subjects With Moderate to Severe Glabellar Lines.

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

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)

NCT05248867Phase 3CompletedPrimary

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

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