A Randomized, Double-Blind Study to Assess the Safety, Efficacy and Tolerability of Oral DFD-29 Capsules for the Treatment of Rosacea.

• Status: Recruiting
• Trial end date: 2022-12-31
• Target enrollment: 0
• Participant gender: All

Summary

This is a 16-week, multicenter, randomized, parallel-group, double-blind, controlled study. After assessing eligibility during a screening period of up to 30 days, approximately 320 subjects at least 18 years old who are diagnosed with moderate to severe papulopustular rosacea will be randomized in a 3:3:2 ratio to DFD-29 (40 mg), Doxycycline capsules 40 mg, or Placebo once daily for 16 weeks.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Journey Medical Corporation
• Collaborator: Dr. Reddy's Laboratories Limited
• Treatments: Doxycycline

Criteria

Key Inclusion Criteria:

• Male and female subjects aged 18 years and above.

• Subjects must be in good general health as determined by the investigator and supported by the medical history.

• Subjects must have a clinical diagnosis of papulopustular rosacea with IGA grade 3 (moderate) or IGA grade 4 (severe) at Baseline.

• Subjects must have 15 to 60 (both inclusive) inflammatory lesions (papules and pustules) of rosacea over the face at Baseline.

• Subjects must have not more than 2 nodules or cysts at Baseline.

Key Exclusion Criteria:

• Female subjects who are pregnant or nursing or planning to become pregnant during the study.

• Male subjects whose female partner is planning to conceive a child.

• Clinically significant abnormal laboratory test results that, in the opinion of the investigator, would compromise the subject's safety or ability to participate in the trial.

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

• History of lupus-like syndrome, autoimmune hepatitis, vasculitis, or serum sickness.

• Any clinically significant condition or situation other than the condition being studied that, in the opinion of the investigator, would interfere with the study evaluations or optimal participation in the study.