Efficacy and Safety of SR1375 in Adult Patients With CAP

Recruiting now · Phase 2 · Has a placebo group

Conditions studied: Community-acquired Pneumonia

In brief

This is a phase 2 study to evaluate the efficacy and safety of SR1375 in hospitalized adult patients with CAP. Patients will receive SR1375 or placebo for 8 weeks. The study duration for each patient is up to 10 weeks.

Key facts

Study ID
NCT06577558
Run by
Shanghai SIMR Biotechnology Co., Ltd.
People needed
240
Starts
2024-09-10
Expected to finish
2025-10-30
Last updated by the study team
2025-07-09

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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