Efficacy and Safety of Faropenem in Bangladeshi Adult Patients With Community-Acquired Bacterial Pneumonia (CABP)
Recruiting
Phase 4
Interventional Study
Pneumonia, Community-Acquired
Bacterial Pneumonia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 160 (estimated)
- Sponsor
- Dr. Md. Alimur Reza · Industry
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About This Trial
The goal of this clinical trial is to evaluate the efficacy and safety of faropenem in comparison to co-amoxiclav and clarithromycin in Bangladeshi adults diagnosed with community-acquired bacterial pneumonia (CABP). Eligible participants will be randomly assigned to one of two treatment arms. The first arm will receive faropenem at a dosage of 200 mg administered three times daily for a duration …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Male or female patients aged between 18 to 65 years.
* Have an acute illness (less than or equal to 7 days duration) with any of the following signs and symptoms consistent with a lower respiratory tract infection (new or worsening):
1. Fever (body temperature \> 38.0 °C (1…
Contacts
Prof. Khan Abul Kalam Azad, MBBS, FCPS, MD(Med), FACP(USA)
+880-1727271414
CONTACT