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NCT04134273 · ClinicalTrials.gov registry record · Phase 1

Bio-equivalence Study With Clinical Endpoints in the Treatment of Acne Vulgaris

A Phase 1 study, sponsored by Sun Pharmaceutical Industries.

Completed
Registry status
Phase 1
Development phase
1,260
Enrollment target

NCT04134273: Completed Phase 1 study, sponsored by Sun Pharmaceutical Industries.

NCT04134273 is a Phase 1 study that has completed, run by Sun Pharmaceutical Industries. The registered enrollment target is 1,260 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (2000% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04134273, a Phase 1 study, has completed, sponsored by Sun Pharmaceutical Industries.

COMPLETED
Registry status
Phase 1
Development phase
1,260 participants
Enrollment target

Study Summary

This study is to evaluate the therapeutic equivalence and safety of Taro Product to RLD in the treatment of acne vulgaris.

Primary Outcome

Demonstration of Bioequivalence in percent change in inflammatory and non-inflammatory lesion counts.

Interventions

  • DRUG Placebo
  • DRUG Clindamycin
  • DRUG CLPG Topical Gel 1%

Trial Details

FieldValue
Enrollment Target 1,260 participants
Start Date 2019-03-20
Est. Completion 2019-10-15
Phase Phase 1
Sun Pharmaceutical Industries

48 total trials

What the finished NCT04134273 record still lists

NCT04134273 is an interventional study that assigns participants to a tested intervention. Its 1,260 participants enrollment target places it among the larger protocols in the corpus, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (2000% higher).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT04134273 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04134273 about?

NCT04134273 is a clinical study titled "Bio-equivalence Study With Clinical Endpoints in the Treatment of Acne Vulgaris". This study is to evaluate the therapeutic equivalence and safety of Taro Product to RLD in the treatment of acne vulgaris.

What is the current status of trial NCT04134273?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 1,260 participants. The study started on 2019-03-20. Estimated completion is 2019-10-15.

What interventions are being tested in trial NCT04134273?

The interventions under investigation include: Placebo (DRUG), Clindamycin (DRUG), CLPG Topical Gel 1% (DRUG).

Who is sponsoring clinical trial NCT04134273?

This trial is sponsored by Sun Pharmaceutical Industries, which has 48 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04134273's enrollment target sits among peer trials

1,260 5th of 2000 higher than 1,996 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04134273, the US trial registry maintained by the National Library of Medicine. NCT04134273 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.