WHO ICTRP trial

Efficacy and Safety Study of Ruxolitinib Cream Followed by an Extension Period…

EUCTR2019-000846-37-FR · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2019-000846-37-FR
Public title Efficacy and Safety Study of Ruxolitinib Cream Followed by an Extension Period in Participants with Vitiligo
Scientific title A Phase 3, Double-Blind, Randomized, Vehicle-Controlled, Efficacy and Safety Study of Ruxolitinib Cream Followed by an Extension Period in Participants With Vitiligo - Topical Ruxolitinib Evaluation in Vitiligo Study 1 (TRuE-V1)
Primary sponsor Incyte Corporation
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no
Countries United States;France;Canada;Spain;Poland;Bulgaria;Netherlands;Germany;United Kingdom;Italy
Conditions Vitiligo MedDRA version: 21.1 Level: PT Classification code 10047642 Term: Vitiligo System Organ Class: 10040785 - Skin and subcutaneous tissue disorders ;Therapeutic area: Diseases [C] - Skin and Connective Tissue Diseases [C17]
Interventions Product Code: INCB018424 PHOSPHATE CREAM 1.5% Pharmaceutical Form: Cream INN or Proposed INN: ruxolitinib (phosphate) CAS Number: 1092939-17-7 Current Sponsor code: INCB018424 phosphate Other descriptive name: RUXOLITINIB PHOSPHATE…
Registration date Dec 13, 2019
Target size 300
Secondary IDs INCB18424-306
Registry page clinicaltrialsregister.eu

At a glance

  • Yes Results available

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

Browse all WHO ICTRP trial registrations