Badalona-barcelone, Spain
- Featured
INCB 18424-303: Topical Ruxolitinib Evaluation in Atopic Dermatitis Study 1 (TRuE-AD1)
NCT03745638 For more information, please contact Incyte Corporation at 1.855.463.3463
Phase
3Span
Sponsor
FOUNTAIN VALLEY, California
Recruiting
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TemPo Studies
**All eligible study participants will receive at no cost:** • Study-related consultation and care • Study visits, tests, assessments, and procedures • Study drugs (investigational drug or placebo)
Phase
N/ASpan
212 weeksSponsor
Cerevel TherapeuticsFountain Valley, California
Recruiting
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Study in Parkinson's Disease Patients With Dyskinesia With Combinations of JM-010 and Its Individual Components
This is a two-part, Phase 2, double-blind, placebo-controlled, randomized, multicentre study. Subjects with a diagnosis of PD and dyskinesias in PD will complete a Screening Visit to assess eligibility to participate in the study.
Phase
2Span
168 weeksSponsor
Bukwang PharmaceuticalFountain Valley, California
Recruiting
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Topical Ruxolitinib Evaluation in Chronic Hand Eczema Study 1 (TRuE-CHE1): A Phase 3, Double-Blind, Randomized, 16-Week, Vehicle-Controlled, Efficacy and Safety Study of Ruxolitinib Cream Followed by an Open-Label Extension Period in Adults With Chronic Hand Eczema
Phase
3Span
86 weeksSponsor
Incyte CorporationFOUNTAIN VALLEY, California
Recruiting
- Featured
We are currently recruiting participants for the BLUEPRINT study. This study investigates the effectiveness, safety, and tolerability of the drug BLU-5937 for chronic itch in people with eczema.
For more information and to register to the study, please visit the study page: **<https://innovaderm.com/studies/blueprint-study-atopic-dermatitis/>**
Phase
2Span
Sponsor
Fountain Valley, California
Recruiting
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Combination Therapies With Adagrasib in Patients With Advanced NSCLC With KRAS G12C Mutation
Phase
2Span
227 weeksSponsor
Mirati Therapeutics Inc.Los Alamitos, California
Recruiting
Fountain Valley, California
Recruiting
A Study of Tildrakizumab in Pediatric Subjects With Chronic Plaque Psoriasis
Phase
2/3Span
621 weeksSponsor
Sun Pharmaceutical Industries LimitedFountain Valley, California
Recruiting
A Safety and Pharmacokinetics Study of IDP-122 Lotion in Pediatric Participants With Plaque Psoriasis
Phase
4Span
245 weeksSponsor
Bausch Health Americas, Inc.Fountain Valley, California
Recruiting
Efficacy and Safety of M281 in Adults With Warm Autoimmune Hemolytic Anemia
The study consists of a 24-week double-blind, placebo control period, a 144-week open-label extension period and follow-up period of 8 weeks after last study drug administration. Eligible participants will be randomized to placebo or nipocalimab (2 dose levels) during the double-blind period and nipocalimab (2 dose levels) during the open-label extension period.
Phase
2/3Span
452 weeksSponsor
Janssen Research & Development, LLCFountain Valley, California
Recruiting