A Study to Assess the Efficacy, Safety and Tolerability of DFD-04

Rosacea Clinical Trial

Official title:

A Multi-center, Randomized, Double-Blind, Parallel-group, Placebo-Controlled Study to Assess the Efficacy, Safety and Tolerability of DFD-04 (Itraconazole) Ointment, 5% in Patients With Inflammatory Lesions of Rosacea Over 12 Weeks

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02828241
• Other study ID #: DFD04-CD-002
• Status: Completed
• Phase: Phase 2
• Start date: July 2016
• Est. completion date: November 2017

Study information

• Verified date: January 2019
• Source: Dr. Reddy's Laboratories Limited
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this exploratory study is to assess the efficacy, safety and tolerability of DFD-04 Ointment for topical treatment of rosacea over 12 weeks of treatment.

Description:

Subjects with mild to moderate papulopustular rosacea (Investigator's Global Assessment [IGA] grade 2-3), a Clinician's Erythema Assessment (CEA) score of 2-3 and 6-30 inflammatory lesions (papules and pustules) were randomized to treatment with DFD-04 ointment or Vehicle ointment in a ratio of 2:1.

During the 12-week treatment period subjects used the IMP twice daily with approximately 12 hours between applications. Subjects were instructed to treat affected skin in a defined treatment area on the face.

The investigator assessed efficacy by using an IGA 5-point scale and CEA 4-point scale and by counting the number of inflammatory lesions on the face at Baseline (Day 1) and Weeks 4, 8 and 12 (End of Treatment [EoT], defined as complete clearance of inflammatory lesions or Week 12, whichever was earlier). Furthermore, a non-invasive biomarker assessment was done by using a Transdermal Analysis Patch (TAP) at Baseline (Day 1) and Weeks 4 and 12.

Safety assessments included investigator's assessment of application site reactions at Baseline (Day 1) and Weeks 4, 8, and 12 for all treated areas.

Other safety assessments included vital signs (blood pressure [BP] and pulse rate) and urine pregnancy tests (UPTs) (only for females), clinical laboratory parameters (serum and urine), extent of exposure, and Adverse Events.

In addition, pharmacokinetic (PK) analysis was performed to evaluate the systemic exposures of itraconazole and its active metabolite, hydroxyl-itraconazole, with blood samples drawn from the first 12 subjects at various pre-specified timepoints.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 61
• Est. completion date: November 2017
• Est. primary completion date: January 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 64 Years

Eligibility

Inclusion Criteria:

1. Subjects must be able to understand the requirements of the study and be willing to give written informed consent.

2. Subjects must be willing to provide authorization to use protected health information.

3. Subjects, any gender or race, must be in good general health as determined by the Investigator

4. Subjects must have a clinical diagnosis of papulopustular rosacea, Investigator's Global Assessment (IGA) grade 2 - 3.

5. Subjects must have 6 - 30 inflammatory lesions (papules and pustules) of rosacea over the face.

6. Subjects must have a Clinician`s Erythema Assessment (CEA) score of 2 - 3.

7. Subjects must have no more than 2 nodules.

8. Subjects must agree to only use the study products and to not use any other treatment for rosacea (prescription or over the counter) or any other skin care or cosmetics product (make-up etc.) on the facial skin of the treatment area during the course of the study.

9. Subjects must be free of any systemic or dermatologic disorder, which in the opinion of the Investigator, will interfere with the study results.

10. Females have a negative urine pregnancy test at the Screening and Baseline Visit.

11. Females must either be postmenopausal with no menses for at least 12 months or surgically sterile (hysterectomy or tubal ligation) or agree to use a reliable method of contraception with a failure rate of less than 1 percent per year when used consistently and correctly.

12. Subject must be in good general health as determined by the investigator and supported by the medical history and normal or not clinically significant abnormal vital signs (blood pressure and pulse).

13. Subject is physically able to apply study product to all affected areas.

Exclusion Criteria:

1. Females who are pregnant or nursing or planning to become pregnant during the study.

2. Subjects who have been treated for rosacea within the 30 days prior to the Baseline Visit.

3. Subjects who have been treated with systemic retinoids within 6 months prior to the Baseline visit.

4. Subjects who have participated in a trial involving any investigational product in the 30 days prior to the Baseline Visit.

5. Subjects with any disease or medical condition that would interfere with the study or place the subject at undue risk especially cardiovascular diseases, reduced lung function (including asthma), renal dysfunction or liver dysfunction.

6. Subjects who have been treated within 30 days prior to baseline visit with methadone,disopyramide, dofetilide, dronedarone, quinidine, ergot alkaloids (such as dihydroergotamine, ergometrine (ergonovine), ergotamine, methylergometrine (methylergonovine)), irinotecan, lurasidone, oral midazolam, pimozide, triazolam, felodipine, nisoldipine, ranolazine, eplerenone, cisapride, lovastatin, simvastatin, ticagrelor, terfenadine, astemizole, mizolastine, eletriptan, as well as lovastatin, simvastatin and atorvastatin and, in subjects with varying degrees of renal or hepatic impairment, colchicine, fesoterodine, telithromycin and solifenacin.

7. Subjects who use or have used systemic steroids within the 30 days prior to the Baseline Visit or any other immunosuppressive medication.

8. Subjects positive for human immunodeficiency virus (HIV), hepatitis B and hepatitis C-test at screening.

9. Subjects who are unable to comply with study requirements.

10. Subjects with other skin diseases that may confound the evaluation of rosacea.

11. History of organ transplant requiring immunosuppression, HIV, or other immune compromised state.

12. Subject who in the opinion of the investigator or physician performing the initial examination the subject should not participate in the trial, e.g. due to probable noncompliance or inability to understand the trial and give adequately informed consent

13. Subject with close affiliation with the investigator (e.g. a close relative) or persons working at the respective trial sites or subject who are an employee of sponsor.

14. Subject institutionalized because of legal or regulatory order.

15. History of drug or alcohol abuse in the last year.

Related Conditions & MeSH terms

• Rosacea

Intervention

Drug:
• DFD-04 Ointment

Other:
• Placebo Ointment

Locations

Country	Name	City	State
Germany	Site 201	Berlin
Germany	Site 208	Berlin
Germany	Site 202	Bochum
Germany	Site 205	Hamburg
Germany	Site 203	Mahlow
Germany	Site 204	Munster
Germany	Site 207	Potsdam
Germany	Site 206	Wiesbaden

Sponsors (1)

Lead Sponsor	Collaborator
Dr. Reddy's Laboratories Limited

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Inflammatory Lesion Counts	Mean change from Baseline in the inflammatory lesion count at the End of Treatment. A lower score at the end of the study compared to Baseline is considered a better outcome.	At the end of study (12 weeks)
Primary	Number of Subjects With Investigator's Global Assessment (IGA) Success	Number of subjects with treatment success based on Investigator's Global Assessment (IGA) score at the End of Treatment, defined as an IGA score of 0 (clear) or 1 (almost clear) with composite grade change from Baseline of at least 2 points.	At the end of study (12 weeks)
Primary	Number of Subjects With Treatment Success by Clinician's Erythema Assessment (CEA) Scale	Number of subjects with Treatment Success defined as a score of 0 or 1 and a 2 grade improvement on the CEA scale from Baseline to 12 weeks.	At end of study (12 weeks)