A Phase 2, multicenter, open-label, non-randomized, proof-of-concept study evaluating the efficacy, safety, and tolerability of SAR445088 in adults with chronic inflammatory demyelinating polyneuropathy (CIDP)
| Sponsor: |
Sanofi |
| Enrolling: |
Male and Female Patients |
| IRB Number: |
AAAT9079 |
| U.S. Govt. ID: |
NCT04658472 |
| Contact: |
Raisy Fayerman: 212-305-6035 / rf2632@cumc.columbia.edu |
This study is a global multicenter, Phase 2, open-label, PoC study evaluating the efficacy, safety, and tolerability of SAR445088 administered to 3 subpopulations of patients with chronic inflammatory demyelinating polyneuropathy (CIDP): patients who are being treated with SOC therapies defined as intravenous immunoglobulin (IVIg), subcutaneous immunoglobulin (SCIg), or corticosteroids; patients with CIDP who are refractory to SOC; and patients with CIDP who are nave to SOC. Adults 18 years of age at the time of signing the informed consent.
This study is closed
Investigator
Thomas Brannagan, MD
| Are you at least 18 years old? |
Yes |
No |
| Have you been diagnosed with CIDP? |
Yes |
No |