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Clinical Trial Summary

This is a randomized, double-Blind, placebo-controlled Phase 2 Study of Orelabrutinib in Patients with Relapsing-Remitting Multiple Sclerosis.


Clinical Trial Description

The study contains 2 parts: Core Part and an Open-label Extension (OLE) Part. The Core Part is a randomized, double-blind, placebo-controlled, phase 2 study. Patients with RRMS will be randomly assigned to 1 of 4 treatment groups. placebo, orelabrutinib (low dose), orelabrutinib (medium dose) and orelabrutinib (high dose) at a 1:1:1:1 ratio. The OLE part is an open-label, single treatment arm study to enroll patients who have completed the Week 24 visit in the Core Part for continued treatment and collect additional long-term safety and efficacy data.All patients will receive the low dose of orelabrutinib or any other dose as suggested from the Core part of the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04711148
Study type Interventional
Source Beijing InnoCare Pharma Tech Co., Ltd.
Contact
Status Active, not recruiting
Phase Phase 2
Start date March 1, 2021
Completion date March 1, 2026

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