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Not Yet RecruitingNCT05497401

A Controlled Study to Evaluate the Efficacy of Allogeneic MesenCure for the Treatment of Patients With ARDS

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
BonusBio Group Ltd · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The efficacy of the allogeneic cell-therapy product MesenCure in addition to standard of care will be evaluated in comparison to placebo control in 300 moderate to severe Covid patients

Conditions

Interventions

TypeNameDescription
BIOLOGICALMesenCureEnhanced mesenchymal cell-based product
OTHERPlaceboSaline

Timeline

Start date
2026-04-01
Primary completion
2028-06-01
Completion
2028-10-01
First posted
2022-08-11
Last updated
2025-08-11

Regulatory

Source: ClinicalTrials.gov record NCT05497401. Inclusion in this directory is not an endorsement.

A Controlled Study to Evaluate the Efficacy of Allogeneic MesenCure for the Treatment of Patients With ARDS (NCT05497401) · Clinical Trials Directory