Status:
COMPLETED
A Study of the Safety and Efficacy of DFD-03 for the Treatment of Acne Vulgaris
Lead Sponsor:
Dr. Reddy's Laboratories Limited
Conditions:
Acne Vulgaris
Eligibility:
All Genders
9+ years
Phase:
PHASE3
Brief Summary
Enrollment of subjects with mild to moderate facial acne. Efficacy was assessed by using an Investigator's Global Assessment scale (IGA 5 point scale) and by counting the number of inflammatory and no...
Detailed Description
Enrollment of subjects with mild to moderate facial acne. Subjects with acne lesions of any severity on the chest and/or back (including shoulders) were enrolled provided they had mild to moderate acn...
Eligibility Criteria
Inclusion
- Main
- Subject must be at least 9 years of age.
- A clinical diagnosis of mild to moderate facial acne vulgaris.
- Inflammatory lesion count (papules and pustules) of at least 20 on the face, Non-inflammatory lesion count (closed and open comedones) of at least 25 on the face and No more than 2 nodulocystic lesions on the face.
- Females, regardless of childbearing potential, if sexually active, must be on or use an acceptable method of birth control.
- Subject must be in good general health as determined by the investigator and supported by medical history, physical and Vital Signs exam.
- Main
Exclusion
- Females who are pregnant or lactating or planning to become pregnant.
- Treatment with the following products:
- Topical acne treatments or other topical facial medication on the treatment area.
- Systemic corticosteroids, systemic acne treatments including systemic antibiotics used for treatment of acne.
- Systemic retinoid use.
- Undertaken certain facial procedures such as chemical peel, laser treatment, photodynamic therapy, acne surgery, cryodestruction or chemodestruction, x-ray therapy, intralesional steroids, dermabrasion, or depilation (except eyebrow shaping).
- Treatment with a medication or procedure that, in the opinion of the investigator, would put the subject at unacceptable risk for participation in the study or may interfere with evaluations in the study.
- Treatment with an investigational product or device in the 30 days.
- Known allergic reaction to retinoids or tazarotene.
- Presence of any facial skin disease or condition that would interfere with the study or place the subject at unacceptable risk including sunburn, rosacea, seborrheic dermatitis, perioral dermatitis, lupus, dermatomyositis, psoriasis, eczema, squamous cell carcinoma, acneiform eruptions caused by medications, steroid acne, steroid folliculitis, bacterial folliculitis or any other facial disease or condition.
- Subjects with a serious and/or chronic medical condition such as chronic or active liver disease, renal impairment, heart disease, severe respiratory disease, rheumatoid arthritis, current malignancies, immunocompromised conditions, or any other disease that, in the opinion of the investigator, would interfere with the study or place the subject at unacceptable risk.
- Subjects who have been in another investigational trial within 30 days.
Key Trial Info
Start Date :
July 31 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 19 2018
Estimated Enrollment :
550 Patients enrolled
Trial Details
Trial ID
NCT03290027
Start Date
July 31 2017
End Date
April 19 2018
Last Update
March 1 2021
Active Locations (1)
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1
Dr. Seemal
Plano, Texas, United States, 75024