A Study Comparing Diclofenac Sodium Gel 3% to Solaraze® Gel 3% in the Treatment of Actinic Keratosis

Phase 1

Completed

• Conditions: Actinic Keratosis
• Interventions: Drug: Diclofenac Sodium Gel 3%; Drug: Vehicle Topical Gel; Drug: Solaraze® (diclofenac sodium) Gel 3%

• Registration Number: NCT01742663
• Lead Sponsor: Taro Pharmaceuticals USA

Brief Summary

The objective of this study is to compare the relative efficacy and safety of the test formulation diclofenac sodium gel 3% (Taro Pharmaceuticals Inc.) to the marketed formulation Solaraze® (diclofenac sodium) Gel 3% (Fougera Pharms) in the treatment of actinic keratosis.

Both the test and reference formulations will also be compared to a placebo formulation to test for superiority.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-10
• Study First Submitted: 2012-12-03
• Study First Submitted QC: 2012-12-04
• Study First Posted: 2012-12-05
• Primary Completion: 2013-07
• Study Completion: 2013-10
• Status Verified: 2014-01
• Last Update Submitted: 2014-01-19
• Last Update Posted: 2014-01-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 435

Inclusion Criteria

• Signed informed consent form.
• Immunocompetent male or non-pregnant, non-lactating female at least 18 years of age.
• Diagnosis of AK with at least 5 and no more than 10 clinically typical, visable, discrete, nonhyperkeratotic, nonhypertrophic AK lesions each at least 4 mm in diameter on the face and/or bald scalp contained within a 25 cm2 treatment area.
• Women either must be 1 year post-menopausal, surgically sterile, or if they are of child-bearing potential they must have been using systemic birth control, IUD or Norplant for at least 28 days prior to treatment start, or used barrier methods consistently at least 14 days before study gel administration, had a normal menstrual cycle for the month prior to the start of treatment, have a negative urine pregnancy test result upon entry into the study and agree to use a medically accepted form of birth control throughout the study period.
• Free from any systemic or dermatologic disorder that, in the opinion of the investigator, will interfere with the study results or increase the risks of AEs.
• Any skin type or race, providing the skin pigmentation will allow discernment of erythema.
• Willingness and capability to cooperate to the extent and degree required by the protocol.

Exclusion Criteria

• Active gastrointestinal ulceration or bleeding.
• Current or history of severe renal or hepatic impairment.
• Presence of atopic dermatitis, basal cell carcinoma, squamous cell carcinoma, eczema, psoriasis, rosacea, sunburn or other possible confounding skin conditions on the face or bald scalp.
• Use within six months prior to randomization of oral isotretinoin.
• Use within six months prior to baseline on the face or bald scalp of chemical peel, dermabrasion, laser abrasion, PUVA therapy or UVB therapy.
• Use within one month prior to baseline on the face or bald scalp of cryodestruction or chemodestruction, curettage, photodynamic therapy, surgical excision, topical 5-fluorouracil, topical corticosteroids, topical diclofenac, topical Imiquimod, topical retinoids or other treatments for actinic keratosis including glycolic acids or over-the-counter products containing retinol, alpha or beta hydroxy acids.
• Use within one month prior to baseline of immunomodulators or immunosuppressive therapies, interferon, systemic corticosteroids or cytotoxic drugs.
• Known allergies to diclofenac sodium, benzyl alcohol, polyethylene glycol monomethyl ether 359, hyaluronate sodium or any excipients in the test or reference gels.
• Receiving 5-Fluorouracil or other systemic cancer chemotherapy within 6 months prior to study entry.
• Any condition, medical, psychological or social, that, in the investigator's opinion, would interfere with participation in the study.
• Women who are pregnant or planning pregnancy or lactating during the study.
• Participation in any investigational drug study within 30 days of enrollment or previous participation in this study.
• Employees or family members of employees of the research center or investigator.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Diclofenac Sodium Gel 3%	Diclofenac Sodium Gel 3%	Diclofenac Sodium Gel 3% (Taro Pharmaceuticals Inc.)
Vehicle Topical Gel	Vehicle Topical Gel	Vehicle Topical Gel (Taro Pharmaceuticals Inc.)
Solaraze® (diclofenac sodium) Gel 3%	Solaraze® (diclofenac sodium) Gel 3%	Solaraze® (diclofenac sodium) Gel 3% (Fougera Pharms)

Primary Outcome Measures

Name	Time	Method
Bioequivalence	Study day 90 (30 days after completion of 60 days of treatment)	Bioequivalence will be determined by evaluating the proportion of patients in the test and reference groups with 100% clearance of all AK lesions in the treatment area.

Secondary Outcome Measures

Name	Time	Method
Superiority to placebo	Study day 90 (30 days after completion of 60 days of treatment)	The superiority of the test and reference gels against the placebo will be tested by the proportion of patients showing 100% clearance of actinic keratosis lesions at Day 90 (30 days after completion of 60 days of treatment)using the modified intent to treat population and last observation carried forward.