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Study Description

Brief Summary
The CUV104 study will assess the efficacy and safety of afamelanotide in patients with vitiligo on the face and body as a monotherapy in repigmentation.
Condition or Disease
Vitiligo
Intervention/Treatment
Afamelanotide
Phase
Detailed Description
N/A

Study Design

Study Type
Enrollment
Allocation
Intervention Model
Masking
Primary Purpose
Official Title
Estimated Study Start Date
Estimated Primary Completion Date
Estimated Study Completion Date

Arms & Interventions

Arm
Intervention

Outcome Measures

Primary Outcome Measures
Secondary Outcome Measures
Other Outcome Measures

Eligibility Criteria

Ages Eligible for Study
18 to 75 Years (Adult, Older Adult)T
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No

Criteria

Inclusion Criteria
Exclusion Criteria

Contacts & Locations

Contacts
Head of Clinical Operations
+441372860765 mail@clinuvel.com
Locations
United States, Michigan CLINUVEL Investigational site Detroit
Sponsors and Collaborators
Investigators

More Information

Other Publications
Responsible Party
Interventional
ClinicalTrials.gov Identifier
Other Study ID Numbers
First Posted
Last Update Posted
Last Verified

Individual Participant Data (IPD) Sharing Statement

Plan to Share IPD
Studies a U.S. FDA-regulated Drug
Product
Studies a U.S. FDA-regulated Device
Product
Keywords provided by Hospices Civils de Lyon
Additional relevant MeSH Terms