Efficacy and Safety Study Comparing CPL409116 to Placebo in Participants With Active Rheumatoid Arthritis
Status:
Recruiting
Trial end date:
2023-08-31
Target enrollment:
Participant gender:
Summary
The purpose of the following phase II clinical trial is to determine safety and effectiveness
of Janus kinases and Rho-kinases inhibitor (JAK/ROCKi) in patients with Rheumatoid arthritis
after oral administration of investigational medicinal product (IMP) called CPL409116. JAK
inhibitors are a new class of small molecule drugs that modulate inflammatory pathways by
blocking one or more JAK receptors. In recent years, JAK inhibitors have emerged as a new
option for the treatment of various inflammatory diseases, including rheumatoid arthritis,
psoriatic arthritis, skin disorders and others. CPL409116 inhibits JAK1 and JAK3 with less
inhibitory activity against JAK2 and Tyk2. Inhibition of these kinases decreases inflammatory
cytokine release which in turn decreases lymphocyte activation and proliferation. Moreover,
CPL409116 blocks Rho-kinases (ROCKs), which are involved in diverse cellular processes
including actin cytoskeleton organization, cell adhesion and motility, proliferation,
apoptosis as well as smooth muscle contraction. ROCKs signalling is one of the major pathways
implicated in the pathogenesis of cardiovascular, renal as well as fibrotic diseases. However
recent data indicate their role in immune cell regulation and inflammatory disease
development. CPL409116 was designed predominantly for the therapy of immune-related diseases:
rheumatoid arthritis (RA) or psoriasis but the unique mode of action of this compound may be
beneficial for patients suffering from fibrotic complications developing on the basis of
autoimmune diseases. RA is a chronic systemic autoimmune disease characterised by persistent
joint inflammation leading to loss of joint function as well as cartilage and bone damage.
Chronic, progressive course of the disease results in disability, reduced quality of life, as
well as higher comorbidity and mortality rates. It is well documented that JAK kinases play a
pivotal role in cytokine receptor signalling to phosphorylate and activate signal transducer
and activator of transcription (STAT) proteins. Several of these JAK-controlled cytokine
receptor pathways are immediately involved in the initiation and progression of RA
pathogenesis. After preclinical studies conducted by Celon Pharma, CPL409116 could have been
classified as a good clinical candidate for the treatment of patients with RA and next,
results obtained after the phase I clinical trial in healthy volunteers confirmed its safety
and a good pharmacokinetic profile.
Phase:
Phase 2
Details
Lead Sponsor:
Celon Pharma SA
Collaborator:
National Center for Research and Development, Poland