Last reviewed · How we verify

NCT06296212

Study of Intravenous TAD® 600 Mg/4 ML Solution for Injection to Evaluate Efficacy and Safety in Preventing Myocardial Injury in Patients with Pneumonia.

Recruiting now Phase 3
What this trial tests

Phase 3 trial testing TAD® 600 mg/4 mL powder and solvent for solution for injection in Pneumonia in 178 participants. Currently enrolling.

Timeline
25 June 2024
30 September 2025

Quick facts

Lead sponsorBiomedica Foscama S.p.A. Industria Chimico-Farmaceutica
PhasePhase 3
StatusRecruiting now
Enrollment178
Start date25 June 2024
Estimated completion30 September 2025

Drugs / interventions tested

Conditions studied

Sponsor

Biomedica Foscama S.p.A. Industria Chimico-Farmaceutica — full company profile →

Who can join

Eligibility, any sex, with Pneumonia or Myocardial Injury.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Pneumonia

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06296212.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing