Phase 2Suspended

Study to Evaluate the Safety, Tolerability, and Activity of CM-101 in Patients With Systemic Sclerosis (ABATE)

A Phase 2, Multicenter, Randomized, Double-Blind, Proof of Biology Study to Evaluate the Safety, Tolerability, and Activity of CM-101 in Patients With Systemic Sclerosis

Sponsor
ChemomAb Ltd. (Industry)
Enrolment
45 planned
Conditions
Systemic Sclerosis
Interventions
10 mg/kg CM-101; Placebo
Ages
adults, older adults
Registry
NCT06210945

From the registry

This study is designed to assess the safety and tolerability of the anti-human CCL24 monoclonal antibody CM-101 in adult patients with systemic sclerosis (SSc). Approximately 45 patients at approximately 40 sites will be randomized in a 2:1 ratio to receive either 10 mg/kg CM-101 or placebo.

Primary outcomes

  • Safety and tolerability will be assessed by treatment-emergent adverse events (TEAEs)
Full record on ClinicalTrials.gov