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NCT03599193 · ClinicalTrials.gov registry record · Phase 2

A Bioavailability Study of DFD-03 Compared to Tazorac® in Patients With Moderate Acne Vulgaris

A Phase 2 study, sponsored by Dr. Reddy's Laboratories Limited.

Completed
Registry status
Phase 2
Development phase
58
Enrollment target

NCT03599193: Completed Phase 2 study, sponsored by Dr. Reddy's Laboratories Limited.

NCT03599193 is a Phase 2 study that has completed, run by Dr. Reddy's Laboratories Limited. The registered enrollment target is 58 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03599193, a Phase 2 study, has completed, sponsored by Dr. Reddy's Laboratories Limited.

COMPLETED
Registry status
Phase 2
Development phase
58 participants
Enrollment target

Study Summary

This was a multicenter, randomized, multiple-dose, laboratory-blinded, open-label, 2-arm, parallel-arm study in subjects with moderate acne vulgaris.

Primary Outcome

The maximum plasma concentration of tazarotenic acid post dosing on Day 21 (Cmax(ss))

Interventions

  • DRUG Tazarotene Cream, 0.1%
  • DRUG Tazarotene Lotion, 0.1%

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2017-10-04
Est. Completion 2018-04-30
Phase Phase 2
Dr. Reddy's Laboratories Limited

52 total trials

What the finished NCT03599193 record still lists

NCT03599193 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 58 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (56% lower).

The record links to 0 conditions, and to 2 interventions - of which Tazarotene Cream, 0.1% is the first listed.

NCT03599193 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03599193 about?

NCT03599193 is a clinical study titled "A Bioavailability Study of DFD-03 Compared to Tazorac® in Patients With Moderate Acne Vulgaris". This was a multicenter, randomized, multiple-dose, laboratory-blinded, open-label, 2-arm, parallel-arm study in subjects with moderate acne vulgaris.

What is the current status of trial NCT03599193?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 58 participants. The study started on 2017-10-04. Estimated completion is 2018-04-30.

What interventions are being tested in trial NCT03599193?

The interventions under investigation include: Tazarotene Cream, 0.1% (DRUG), Tazarotene Lotion, 0.1% (DRUG).

Who is sponsoring clinical trial NCT03599193?

This trial is sponsored by Dr. Reddy's Laboratories Limited, which has 52 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03599193's enrollment target sits among peer trials

58 1135th of 2000 higher than 860 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03599193, the US trial registry maintained by the National Library of Medicine. NCT03599193 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.