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Clinical trialNCT00687908CompletedPhase 3Interventional

Adapalene-Benzoy Peroxide (BPO) Gel in the Treatment of Acne Vulgaris as a 6-month Maintenance

SponsorGalderma R&DEnrollment243Acne
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to demonstrate the efficacy of Adapalene 0.1% /Benzoyl Peroxide 2.5% Gel compared to its Vehicle Gel as an acne maintenance treatment in Subjects previously treated with Adapalene-BPO Gel or Adapalene-BPO Vehicle Gel both associated with Doxycycline Hyclate 100 mg. The safety of the two investigational treatments will also be assessed.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

33 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • Galderma Investigational Site

    Barrie, Ontario, Canada

  • Galderma Investigational Site

    North Bay, Ontario, Canada

  • Galderma Investigational Site

    Windsor, Ontario, Canada

  • Galderma Investigational Site

    Québec, Quebec, Canada

Puerto Rico
  • Galderma Investigational Site

    Aibonito, Puerto Rico

  • Galderma Investigational Site

    Carolina, Puerto Rico

United States
  • Galderma Investigational Site

    San Diego, California, United States

  • Galderma Investigational Site

    Denver, Colorado, United States

  • Galderma Investigational Site

    Longmont, Colorado, United States

  • Galderma Investigational Site

    Miami, Florida, United States

  • Galderma Investigational Site

    Snellville, Georgia, United States

  • Galderma Investigational Site

    Chicago, Illinois, United States

  • Galderma Investigational Site

    Evansville, Indiana, United States

  • Galderma Investigational Site

    Overland Park, Kansas, United States

  • Galderma Investigational Site

    Louisville, Kentucky, United States

  • Galderma Investigational Site

    Detroit, Michigan, United States

  • Galderma Investigational Site

    Fort Gratiot, Michigan, United States

  • Galderma Investigational Site

    Fridley, Minnesota, United States

  • Galderma Investigational Site

    Omaha, Nebraska, United States

  • Galderma Investigational Site

    Albuquerque, New Mexico, United States

  • Galderma Investigational Site

    Stony Brook, New York, United States

  • Galderma Investigational Site

    Winston-Salem, North Carolina, United States

  • Galderma Investigational Site

    Warren, Ohio, United States

  • Galderma Investigational Site

    Hazleton, Pennsylvania, United States

  • Galderma Investigational Site

    Hershey, Pennsylvania, United States

  • Galderma Investigational Site

    Simpsonville, South Carolina, United States

  • Galderma Investigational Site

    Arlington, Texas, United States

  • Galderma Investigational Site

    Austin, Texas, United States

  • Galderma Investigational Site

    College Station, Texas, United States

  • Galderma Investigational Site

    Houston, Texas, United States

  • Galderma Investigational Site

    Lubbock, Texas, United States

  • Galderma Investigational Site

    San Antonio, Texas, United States

  • Galderma Investigational Site

    Webster, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Adapalene 0.1% / Benzoyl Peroxide 2.5% GelVehicle Gel
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Nov 2008
Primary completion
31 Jul 2009
Completion
31 Jul 2009
Last update posted
18 Feb 2021
Registered enrollment
243
Registry id
NCT00687908

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.