drugset / Trial / NCT03598751

Clinical Study of Efficacy and Safety of BCD-085 (Monoclonal Anti-IL-17 Antibody) in Psoriatic Arthritis

NCT03598751 ↗

Phase 3 Completed 194 enrolled Biocad
RandomizedParallel-groupDouble-blindTreatment

Summary

Study BCD-085-8/PATERA is a multicentre double-blind placebo-controlled Phase 3 study in patients with psoriatic arthritis (PsA). The objective of the study is to evaluate the efficacy and safety of BCD-085 comparing to placebo in patients with PsA.

Timeline

Start
2018-07-25
Primary completion
2019-06-26
Completion
2022-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject BCD-085 Monoclonal antibody 120 mg Subcutaneous

Indications