Safety and Efficacy Study of AM001 Cream in the Treatment of Actinic Keratosis

NCT03210740 | Completed Phase 2 FDA Drug

• 1 other identifier: AD-AM001-AK1
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

To compare the safety and efficacy profiles of AM001 Cream, 7.5% and its vehicle cream in the treatment of Actinic Keratosis (AK) Lesions

Conditions

Actinic Keratosis

Outcome Measures

Primary Outcomes (1)

• Complete clearance of all lesions

  (100 % of all AK lesions cleared) 8 weeks post treatment

  8 weeks post treatment

Secondary Outcomes (3)

• Complete clearance of all baseline lesions weeks of treatment

  16 weeks

• Complete clearance of all lesions

  12 weeks

• Complete clearance of all lesions

  8 weeks

Study Arms (2)

AM001 Cream, 7.5%

EXPERIMENTAL

A white to off-white Cream free from any foreign particles

Drug: AM001 Cream, 7.5%

Vehicle Cream

PLACEBO COMPARATOR

A white to off-white Cream free from any foreign particles

Drug: Vehicle Cream

Interventions

AM001 Cream, 7.5% DRUG

Active Cream

Also known as: Potassium Dobesilate

AM001 Cream, 7.5%

Vehicle Cream DRUG

Placeo

Also known as: Placebo Cream

Vehicle Cream

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Subject must provide written informed consent.
• Subject must be male or non-pregnant females of any race, and any skin type aged 18 to 80 years both inclusive.
• Subject has 4 to 8 clinically typical, visible, discrete, nonhyperkeratotic, nonhypertrophic AK lesions, each at least 4 mm in diameter within a 25cm² contiguous treatment area on the face or the balding scalp.
• Subject is willing to avoid exposure to sunlight, use of tanning booths, sunlamps, or nonprescription UV (ultra-violate) light sources during the study period.ooths, sunlamps, or nonprescription UV (ultra-violate) light sources during the study period.
• If female subject of childbearing potential, the subject must have a negative urine pregnancy test at Visit 1/ Screening and must have been using an acceptable form of birth control for at least 2 months prior to Visit 1/ Screening and is willing to continue birth control during the study.
• Subject must be willing and able to understand and comply with the requirements of the study, apply the assigned investigational product as instructed, return for the required study visits, comply with therapy prohibitions.
• Subject must be in good health, as confirmed by medical history and physical exam, and free from any clinically significant disease/condition, other than actinic keratosis, that might interfere with the study evaluations.

You may not qualify if:

• Subject has very thick and/or hyperkeratotic actinic keratosis AK lesions in the treatment area.
• Subject has used topical treatment of actinic keratosis in the treatment area with 5-fluorouracil, imiquimod, diclofenac, corticosteroids or retinoids within 1 month prior to Visit 2/Baseline or during the study.
• Subject has used treatment with PDT (photodynamic therapy) or physical therapies (e. g. cryotherapy, curettage or surgical treatment) in the treatment area within 1 month prior to Visit 2/Baseline or during the study.
• Subject has used chemical peel, dermabrasion, laser abrasion, PUVA (prosalen plus ultraviolet A) therapy or UVB therapy within 6 months prior to Visit 2/Baseline or during the study.
• Subject has used immunomodulators or immunosuppressive therapies, interferon, oral corticosteroids, oral retinoids or cytotoxic drugs within 1 month prior to Visit 2/Baseline or during the study.
• Subject has untreated basal cell carcinoma, squamous cell carcinoma or melanoma in the treatment area.
• Subject has suntan or tattoos that may interfere with the assessments in the treatment area.
• Subject has dermatological diseases in the treatment area that may interfere with the assessments, e.g. acute skin inflammation, atopic dermatitis, eczema, rosacea, psoriasis, seborrheic dermatitis, peri-oral dermatitis or hyperpigmentation.
• Subject who consumes excessive amount of alcohol, abuse or have any condition that in the investigator's opinion would compromise compliance, with this protocol.
• Subject has history of malignancy not in remission for at least 5 years excluding basal cell carcinoma and nonperiorificial squamous cell carcinoma of the skin.
• Female subject who is pregnant, nursing or planning a pregnancy within the study participation period
• Subject has symptoms of a clinically significant illness that may influence the outcome of the study in the 4 weeks prior to Visit 1/Screening.
• Subject has participated in another clinical trial involving investigational product or device in the 4 weeks prior to Visit 1/Screening.
• Subject has known allergic reactions to components of the investigational product.

Sponsors & Collaborators

• AmDerma: lead

Study Sites (1)

AmDerma Pharmaceuticals, LLC

High Point, North Carolina, 27262, United States

Location

MeSH Terms

Conditions

Keratosis, Actinic

Interventions

potassium dobesilate

Condition Hierarchy (Ancestors)

Precancerous Conditions; Neoplasms; Keratosis; Skin Diseases; Skin and Connective Tissue Diseases

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 5, 2017
• First Posted: July 7, 2017
• Study Start: June 6, 2017
• Primary Completion: February 13, 2018
• Study Completion: April 24, 2018
• Last Updated: April 30, 2019

Record last verified: 2018-09

Locations

US (1)