Overview

LYT-100 in Post-acute COVID-19 Respiratory Disease

Status:
Recruiting
Trial end date:
2021-12-01
Target enrollment:
Participant gender:
Summary
This study is being conducted in two parts, A and B. Part A is a randomized, double-blind, parallel arm study to evaluate the safety and efficacy of LYT-100 compared to placebo in adults with post-acute COVID-19 respiratory complications. Part B is an Open Label Extension (OLE) study for patients who complete Part A.
Phase:
Phase 2
Details
Lead Sponsor:
PureTech
Collaborators:
Clinipace Worldwide
Novotech (Australia) Pty Limited