Therapeutic Equivalence of Diclofenac Sodium Gel 3% vs Solaraze ® in the Treatment of Actinic Keratosis

Completed · Phase 3 · Has a placebo group

Conditions studied: Actinic Keratoses

In brief

Therapeutic Equivalence of Diclofenac Sodium Gel 3% and Solaraze ®, in the treatment of Actinic Keratosis

Key facts

Study ID

NCT03826550

Run by

Encube Ethicals Pvt. Ltd.

People needed

655

Starts

2018-01-12

Expected to finish

2018-07-03

Last updated by the study team

2019-02-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Signed Institutional Review Board (IRB)-approved informed consent form that meets all criteria of current Food and Drug Administration regulations.
• Male or non-pregnant, non-lactating female, 18 years of age or older.
• Diagnosis of AK with at least five and no more than ten clinically typical, visible, discrete, non-hyperkeratotic, non-hypertrophic AK lesions, each at least 4 mm in diameter, contained within a contiguous 25 cm2 treatment area on the face and/or bald scalp.
• Females of childbearing potential must not be pregnant or lactating at Visit 1 (as confirmed by a negative urine pregnancy test with a sensitivity of less than 50 mIU/ mL or equivalent units of human chorionic gonadotropin). Women of childbearing potential must agree to the use of a reliable method of contraception (e.g., total abstinence, intrauterine device, a double-barrier method, oral, transdermal, injected, or implanted non-hormonal or hormonal contraceptive) throughout the study. Female patients using hormonal contraceptives should have been on the same product/dosing regimen for at least 28 days before Visit 1 and should not change this regimen during the study. A sterile sexual partner is not considered an adequate form of birth control.
• Skin pigmentation that will allow discernment of erythema.

You may not qualify if…

• Females who are pregnant, lactating or planning to become pregnant during the study period.
• Active gastrointestinal ulceration or bleeding.
• Current evidence or history of severe renal or hepatic impairment.
• Known allergy or hypersensitivity to diclofenac, benzyl alcohol, polyethylene glycol monomethyl ether 359, hyaluronate sodium or other excipients in the test, reference or vehicle gel.
• Known allergy or hypersensitivity to other NSAIDs, including aspirin.
• Presence of atopic dermatitis, basal cell carcinoma, squamous cell carcinoma, eczema, psoriasis, rosacea, sunburn, exfoliative dermatitis, open or recent skin wounds, active infections or other possible skin conditions on the face or bald scalp that in the Investigator's opinion would interfere with the study assessments or put the patient at risk.
• Use of oral isotretinoin within six months before randomization.
• Use within six months before Visit 1 on the face or bald scalp of 1) chemical peel, 2) dermabrasion, 3) laser abrasion, 4) PUVA (psoralen plus ultraviolet A) therapy, or 5) UVB therapy.
• Use within one month before Visit 1 on the face or bald scalp of 1) cryodestruction or chemodestruction, 2) curettage, 3) photodynamic therapy, 4) surgical excision, 5) topical 5-fluorouracil, 6) topical corticosteroids, 7) topical diclofenac, 8) topical imiquimod, 9) topical retinoids, or 10) other treatments for AK including glycolic acids or over the- counter (OTC) products containing retinol, alpha or beta hydroxy acids. The occasional use of ophthalmic, intranasal or inhaled corticosteroids (e.g., management of allergic conjunctivitis) is acceptable and not reason for exclusion. Use of inhaled corticosteroids for the management of chronic and stable conditions (e.g., persistent asthma and chronic obstructive pulmonary disease [COPD]) is acceptable as long as it has been on a stable dose for a minimum of three months before the start of the study and up to 1 mg/day.
• Use within one month before Visit 1 of 1) immunomodulators or immunosuppressive therapies, 2) interferon, 3) systemic corticosteroids or 4) cytotoxic drugs.
• Receipt of 5-Fluorouracil or other systemic cancer chemotherapy within 6 months before Visit 1.
• Any condition, medical, psychological, or social, that, in the Investigator's opinion, would interfere with participation in the study or put the patient at risk.
• Inability to understand the requirements of the study and the relative information or are unable or not willing to comply with the study protocol.
• Receipt of any drug as part of a research study within 30 days before Visit 1.
• Employees of the Investigator or research center or their immediate family members.
• Patients who have participated in this study previously.

Where it is running

• Dermatology Trial Associates — Bryant, Arkansas, United States
• West Coast Research — San Ramon, California, United States
• Universal Medical and Research Center, LLC — Coral Gables, Florida, United States
• Solutions Through Advanced Research, Inc. — Jacksonville, Florida, United States
• Health Awareness, Inc. — Jupiter, Florida, United States
• Multi-Speciality Research Associates, Inc. — Lake City, Florida, United States
• FXM Research — Miami, Florida, United States
• FXM Research Miramar — Miramar, Florida, United States
• Ormond Medical Arts Pharmaceutical Research Center — Ormond Beach, Florida, United States
• Moore Clinical Research — Tampa, Florida, United States
• Forward Clinical Trials — Tampa, Florida, United States
• Northwest Clinical Trials — Boise, Idaho, United States
• DS Research — New Albany, Indiana, United States
• DS Research — Louisville, Kentucky, United States
• Minnesota Clinical Study Center — Fridley, Minnesota, United States
• DTRL, Inc. — Henderson, Nevada, United States
• Dermatology Consulting Services — High Point, North Carolina, United States
• Sterling Research Group — Cincinnati, Ohio, United States
• DermDox Centers for Dermatology — Hazleton, Pennsylvania, United States
• PEAK Research, LLC — Upper Saint Clair, Pennsylvania, United States
• Anderson Dermatology — Anderson, South Carolina, United States
• Greenville Dermatology, LLC — Greenville, South Carolina, United States
• Sirius Clinical Research, LLC — Austin, Texas, United States
• Health Research of Hampton Roads, Inc. — Newport News, Virginia, United States

Full record on ClinicalTrials.gov

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