Instituto de Reumatologia | Mendoza, Argentina
Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
About
The purpose of this Proof of Concept (PoC) and Dose-finding (DF) basket study is to evaluate the efficacy and safety of orally administered Enpatoran over 24 weeks in systemic lupus erythematosus (SLE) and cutaneous lupus erythematosus (CLE; subacute cutaneous lupus erythematosus [SCLE] and/or discoid lupus erythematosus [DLE]) participants in a randomized, double-blind, placebo-controlled, parallel, adaptive and dose-ranging setting. Study Duration: 33 weeks Visit Frequency: every 2 or 4 weeks Enpatoran is not available through an expanded access program.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
532 participants in 8 patient groups, including a placebo group
Loading...
Central trial contact
Communication Center; US Medical Information
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal