Bioequivalence Study of Generic Fluorouracil 0.5% Cream and 0.5% Carac® and Placebo

NCT ID: NCT01354717

Last Updated: 2014-10-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 377 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-09-30
• Study Completion Date: 2011-03-31

Brief Summary

This is a double-blind, randomized, placebo-controlled, three treatment parallel study in which normal, healthy men and women (age 45-85) with actinic keratosis will be treated on the face once daily for two weeks with 5-Fluorouracil Cream 0.5%, Spear Pharmaceuticals (Generic), Carac® Cream 0.5% (Brand), or Cream Vehicle (Placebo). Actinic keratoses will be counted at the baseline visit and at the visit four weeks following cessation of treatment.

Detailed Description

actinic keratosis

Conditions

Actinic Keratoses

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Brand Carac

Treatment of actinic keratosis with active ingredient

Group Type: ACTIVE_COMPARATOR

Brand Carac

Intervention Type: DRUG

treatment of actinic keratosis

Generic 0.5% 5-fluorouracil cream

Treatment of actinic keratosis with active ingredient

Group Type: ACTIVE_COMPARATOR

Generic 0.5% 5-fluorouracil cream

Intervention Type: DRUG

treatment of actinic keratosis

Placebo

treatment of actinic keratosis with placebo cream

Group Type: PLACEBO_COMPARATOR

Placebo cream

Intervention Type: OTHER

treatment of actinic keratosis

Interventions

Brand Carac

treatment of actinic keratosis

Intervention Type: DRUG

Generic 0.5% 5-fluorouracil cream

treatment of actinic keratosis

Intervention Type: DRUG

Placebo cream

treatment of actinic keratosis

Intervention Type: OTHER

Other Intervention Names

5-fu; 5-fu

Eligibility Criteria

Inclusion Criteria

Men and women with the presence of actinic keratoses

• Women who have had surgical sterilization or are post-menopausal (absence of menses for at least one year) are eligible. Women of child-bearing potential who are non-pregnant and non-nursing, and willing to avoid pregnancy during the course of the study and during the menstrual cycle following completion of their participation in the study are eligible. (Adequate contraception is defined as regular use of, diaphragm with condoms, IUD with condoms, or systemic contraceptives - if used for at least three months prior to enrollment in the study). A negative pregnancy test is required at entry into the study
• Able to refrain from the use of all other topical medications to the facial area during the treatment period
• Considered reliable and capable of understanding their responsibility and role in the study
• Have provided written informed consent

Exclusion Criteria

• History of allergy or hypersensitivity to 5-fluorouracil

• Known dihydropyrimidine dehydrogenase (DPD) enzyme deficiency
• Clinical evidence of severe, uncontrolled auto-immune, cardiovascular, gastrointestinal, hematological, hepatic, neurological, pancreatic, pulmonary or renal disease
• Dermatologic conditions if present on the face such as: atopic dermatitis, basal cell carcinoma, eczema, psoriasis, rosacea, squamous cell carcinoma, or albinism
• Positive urine pregnancy test in women of child-bearing potential
• Inability to use adequate birth control measures for women of child-bearing potential, as defined above
• Serious psychological illness
• Significant history (within the past year) of alcohol or drug abuse
• Participation in any clinical research study during the 30 day period preceding study initiation
• Medical history which, based on the clinical judgment of the investigator, implies an unlikelihood of successful completion of the study
• Treatment for actinic keratosis or skin cancer in the previous 28 days with the following: topical 5 fluorouracil, cryodestruction (liquid nitrogen spray), curettage (scraping of pre-cancer or skin cancers), surgical removal of skin cancer, photodynamic therapy, surgical excision, topical diclofenac (Solaraze), topical imiquimod (Aldara), topical retinoids if used for actinic keratosis or other treatments for actinic keratoses
• Application of 1) chemical peel, 2) dermabrasion, 3) laser abrasion, 4) PUVA (psoralen plus ultraviolet A) therapy, or 5) UVB therapy to the face or bald scalp within six months prior to randomization
• Use of sun lamps or sun tanning beds or booths during the 2 weeks prior to first application until Day 42 visit
• Any oral (systemic steroids) or topical corticosteroids within 1 month of study entry, except for subjects on chronic low dose corticosteroids less than 5 mg daily for greater than 1 year
• Use within 1 month of any immunomodulators like interferon, or cytotoxic drugs
• Prior treatment with systemic 5-fluorouracil or systemic cancer therapy within 6 months of study entry
• Subjects with lesions suspicious for squamous cell carcinoma

• Minimum Eligible Age: 45 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Spear Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Melanie Appell, M.D.

Role: PRINCIPAL_INVESTIGATOR

Alliance Clinical Research, Inc

Other Identifiers

Spear 0.5%

Identifier Type: -

Identifier Source: org_study_id