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CompletedNCT01206348Updated Nov 30, 2011

Combination Treatment for Moderate to Severe Acne

A Phase 4 interventional study of Minocycline, Clindamycin, Tretinoin, Benzoyl Peroxide in Acne, sponsored by Medicis Global Service Corporation. Completed at 10 sites in United States. Open to participants aged 12 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-11-30.

Sponsored by Medicis Global Service Corporation · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
97
Allocation
Non-randomized
Ages
12 Years to 30 Years
Sex
All
01

Study summary

To determine if a combination of three currently approved acne products are safe and effective for the treatment of moderate to severe acne

Read the detailed description

A Phase IV, Open-Label Study Evaluating the treatment for Combination Acne Therapy.

02

Conditions studied

  • Acne

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Keywords

  • Acne
03

In context

Acne Vulgaris

730 studies on the registry are indexed under Acne Vulgaris; 86 are open to participants now.

This study's enrollment of 97 is above the median of 69 across 628 interventional studies indexed under Acne Vulgaris.

Browse Acne Vulgaris studies →

Lead sponsor

Medicis Global Service Corporation is the lead sponsor of 12 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • moderate to severe acne, IGA = 3 or 4 (Investigator Global Assessment)

Exclusion criteria

Exclusion Criteria:

  • pregnancy and allergies
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
97 participants (actual)

Study arms

  • Experimental
    Open Label Combination

    Solodyn, Ziana, Triaz FC

    Drug: Minocycline, Clindamycin, Tretinoin, Benzoyl Peroxide

Interventions

  • DrugMinocycline, Clindamycin, Tretinoin, Benzoyl Peroxide

    Solodyn 1 tablet, Q day Ziana Gel, topical Q am Triaz FC, topical Q night

06

What researchers measure

Primary outcomes

  1. Proportion of patients showing improvement from Baseline and Week 12

    Time frame: Week 12

07

Study locations

10 sites
  • Birmingham, Alabama, United States
  • Santa Monica, California, United States
  • Hockessin, Delaware, United States
  • Chestnut Hill, Massachusetts, United States
  • Detroit, Michigan, United States
  • Henderson, Nevada, United States
  • High Point, North Carolina, United States
  • Hershey, Pennsylvania, United States
  • Nashville, Tennessee, United States
  • Salt Lake City, Utah, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 30, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01206348
Lead sponsor
Medicis Global Service Corporation
Responsible party
Sponsor
First posted
Sep 21, 2010
Start date
Sep 2010
Primary completion
Jul 2011
Completion
Jul 2011
Last update
Nov 30, 2011

Study contacts

Mary Sanstead, BSN, CCRP
study chair · Medicis Global Service Corporation

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2011. You cannot join it, but the record below documents what was studied.

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