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NCT02899000 · ClinicalTrials.gov registry record · Phase 4

A Treatment for Severe Inflammatory Acne Subjects

A Phase 4 study of Acne Vulgaris, sponsored by Galderma R&D.

Completed
Registry status
Phase 4
Development phase
186
Enrollment target
1
Study location

NCT02899000 is a Phase 4 study of Acne Vulgaris that has completed, run by Galderma R&D. The registered enrollment target is 186 participants, below the 273-participant average among 67 other Acne Vulgaris trials with a reported enrollment target (32% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02899000, a Phase 4 study of Acne Vulgaris, has completed, sponsored by Galderma R&D.

COMPLETED
Registry status
Phase 4
Development phase
186 participants
Enrollment target
1
Study location

Study Summary

Demonstrate that a daily treatment regimen of adapalene 0.3%/benzoyl peroxide 2.5% gel + oral Doxycycline 200 mg is effective and safe in severe inflammatory acne with 3 or fewer nodules or cysts (non-nodulocystic) during a 12-week treatment period.

Conditions Studied

Interventions

  • DRUG Adapalene 0.3% / benzoyl peroxide 2.5% emulsion gel
  • DRUG Oral doxycycline hyclate

Study Locations (1)

Texas

  • Galderma Laboratories, LP - Fort Worth

Trial Details

FieldValue
Enrollment Target 186 participants
Start Date 2016-07-29
Est. Completion 2017-06-27
Phase Phase 4

Sponsor

Galderma R&D

158 total trials

What the Registry Record Tells You About NCT02899000

The ClinicalTrials.gov registry entry for NCT02899000 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 186 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 273-participant average among 67 other Acne Vulgaris trials with a reported enrollment target (32% lower). The listed sponsor is Galderma R&D, which has 158 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Acne Vulgaris appearing as the primary indexed condition, and to 2 interventions - of which Adapalene 0.3% / benzoyl peroxide 2.5% emulsion gel is the first listed.

NCT02899000 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT02899000 about?

NCT02899000 is a clinical study titled "A Treatment for Severe Inflammatory Acne Subjects". Demonstrate that a daily treatment regimen of adapalene 0.3%/benzoyl peroxide 2.5% gel + oral Doxycycline 200 mg is effective and safe in severe inflammatory acne with 3 or fewer nodules or cysts (non-nodulocystic) during a 12-week treatment period.

What is the current status of trial NCT02899000?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 186 participants. The study started on 2016-07-29. Estimated completion is 2017-06-27.

What conditions does trial NCT02899000 study?

This clinical trial studies the following conditions: Acne Vulgaris.

What interventions are being tested in trial NCT02899000?

The interventions under investigation include: Adapalene 0.3% / benzoyl peroxide 2.5% emulsion gel (DRUG), Oral doxycycline hyclate (DRUG).

Who is sponsoring clinical trial NCT02899000?

This trial is sponsored by Galderma R&D, which has 158 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02899000 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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