Evaluation of AMG 714 for Vitiligo

PHASE2CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

December 11, 2020

Primary Completion Date

October 16, 2024

Study Completion Date

April 22, 2025

Conditions
Vitiligo
Interventions
BIOLOGICAL

AMG 714

anti-IL-15 monoclonal antibody (Anti-IL-15 MAB)

BIOLOGICAL

Placebo

Placebo for AMG 714

PROCEDURE

nbUVB phototherapy

Participants will undergo narrow band ultraviolet B (nbUVB) phototherapy if their total body Vitiligo Area Scoring Index (T-VASI) does not improve by ≥ 25% at Week 24 compared to Week 0. Phototherapy will be administered in accordance with the Vitiligo Working Group expert recommendations.

Trial Locations (8)

11042

Northwell Health, Lake Success

19104

Perelman School of Medicine, University of Pennsylvania: Department of Dermatology, Philadelphia

48202

Henry Ford Health System, Detroit

92697

University of California, Irvine: Department of Dermatology, Irvine

95816

University of California Davis Health System: Department of Dermatology, Sacramento

06824

Yale University School of Medicine: Department of Dermatology, New Haven

02111

Tufts Medical Center: Department of Dermatology, Boston

01605

University of Massachusetts Medical School, Worcester

Sponsors

Collaborators (2)

All Listed Sponsors
collaborator

Immune Tolerance Network (ITN)

NETWORK

collaborator

PPD Development, LP

INDUSTRY

collaborator

Rho Federal Systems Division, Inc.

INDUSTRY

collaborator

Amgen

INDUSTRY

lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH