drugset / Trial / NCT05938036

Study of Safety and Efficacy of ALT-100mAb in Participants With Moderate/Severe ARDS

NCT05938036 ↗

Phase 2 Active not recruiting 15 enrolled Aqualung Therapeutics Corp.
RandomizedParallel-groupDouble-blindTreatment

Summary

A Phase 2a, multi-center, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of ALT-100mAb in patients with moderate to severe ARDS.

Timeline

Start
2023-12-01
Primary completion
2027-05-01
Completion
2027-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject ALT-100 Monoclonal antibody 0.4 mg/kg Intravenous
Subject ALT-100 Monoclonal antibody 1 mg/kg Intravenous