Eight Week Study of Treatment With DFD-07 for Actinic Keratosis of the Face and Scalp

NCT02654717 | Completed Phase 2 Results

• 1 other identifier: DFD-07-CD-001
• Study Type: interventional
• Target: 111
• Locations: 1 country
• Sites: 3

Brief Summary

The purpose of this study is to see how well DFD-07 works in treating actinic keratosis on the face and scalp during 8 weeks of treatment. The study will also look at any unwanted effects of the study drug.

Conditions

Actinic Keratosis

Outcome Measures

Primary Outcomes (1)

• Percent of Patients With Complete Clearance of Lesions

  Percent of patients with complete clearance of actinic keratosis (AK) lesions at the end of treatment (8 weeks)

  8 weeks

Study Arms (2)

DFD-07 cream

EXPERIMENTAL

DFD-07 cream applied twice daily

Drug: DFD-07 Cream

Placebo cream

PLACEBO COMPARATOR

Placebo cream applied twice daily

Drug: Placebo Cream

Interventions

DFD-07 Cream DRUG

DFD-07 cream

Placebo Cream DRUG

Placebo cream

Eligibility Criteria

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

You may qualify if:

• To be eligible for the study, the patients have to fulfil all of the following criteria at Visit 1:
• Written informed consent has been signed and dated prior to any study related procedure or initiation of a wash out period
• Skin type I, II or III according to Fitzpatrick
• Actinic Keratosis (AK) mild to moderate grade lesions in an approximately 25 cm2 region of scalp, forehead or face that are non-hypertrophic and non-hyperkeratotic
• years of age or older
• Female patients of childbearing potential must agree to use contraception during the study which can include abstinence with a secondary contraceptive option should the patient become sexually active. All women of childbearing potential must have a negative urine pregnancy test (test must have a sensitivity of at least 25 IU/ML for human chorionic gonadotropin) at the Baseline Visit. A female is considered of childbearing potential unless she is pre-menarche, postmenopausal with no menses for at least 12 months or surgically sterile. Reliable methods of contraception are hormonal methods or intrauterine devices in use for at least 90 days prior to the Baseline Visit or barrier methods plus spermicide use for at least 14 days prior to the Baseline Visit or a partner who has had a vasectomy at least 3 months prior to the Baseline Visit.
• ≥ 60 days washout from prohibited medications:
• Masoprocol
• Fluorouracil
• Cyclosporine
• Retinoids
• Trichloroacetic Acid/Lactic Acid Peel
• % Glycolic Acid Peel
• Topical or systemic diclofenac, celecoxib or any other non-sterioda anti-inflammatory drug (however daily low-dose aspirin is allowed, as long as the patient has been on a stable dose, ≤ 100 mg once a day, for 60 days prior to the start of the study.) Note: Patients may use acetaminophen/paracetamol as needed
• Photodynamic therapy

You may not qualify if:

• Patients who fulfil one or more of the following criteria, will not be eligible for the study:
• Known or suspected hypersensitivity to any non-steroidal anti-inflammatory drug (NSAID) or a component of the formulation of the study medication
• Clinical evidence of severe, uncontrolled autoimmune, cardiovascular, gastrointestinal, hematological, hepatic, neurologic, pulmonary or renal disease.
• Significant history (within the past year) of alcohol or drug abuse
• Participation in any clinical research study within 60 days of the Baseline Visit.
• Pregnancy, lactation or plans to become pregnant
• Concomitant use of cosmetics or other topical drug products on or near the selected treatment area. However, the use of topical sunscreens is allowed.
• Cosmetic or therapeutic procedures (e.g. laser, peeling, photodynamic therapy) within 2 weeks and within 2 cm of the selected treatment area.
• Other skin conditions within the selected treatment area (e.g. rosacea, psoriasis, atopic dermatitis, eczema, basal or squamous cell carcinoma or albinism)
• Use of sun lamps or tanning beds or booths during the 14 days prior to the Baseline Visit or planned use during the study.
• Any systemic cancer therapy within 6 months of the Baseline Visit

Sponsors & Collaborators

• Promius Pharma, LLC: lead

Study Sites (3)

Site One

Bochum, 44791, Germany

Location

Site Two

Bonn, 53111, Germany

Location

Site Three

Wuppertal, 42287, Germany

Location

MeSH Terms

Conditions

Keratosis, Actinic

Condition Hierarchy (Ancestors)

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

Results Point of Contact

• Title: Dr. Srinivas Sidgiddi
• Organization: Dr. Reddy's Laboratories Inc.

srinivassidgiddi@drreddys.com

6093759900

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

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

Study Record Dates

• First Submitted: December 24, 2015
• First Posted: January 13, 2016
• Study Start: November 1, 2015
• Primary Completion: August 1, 2016
• Study Completion: August 1, 2016
• Last Updated: March 17, 2020
• Results First Posted: February 18, 2019

Record last verified: 2020-03

Data Sharing

• IPD Sharing: Will not share

Locations

DE (3)