Efficacy and Safety Study of Intravenous to Oral Solithromycin (CEM-101) Compared to Intravenous to Oral Moxifloxacin in Treatment of Patients With Community-Acquired Bacterial Pneumonia

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A RANDOMIZED, DOUBLE-BLIND, MULTI-CENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF INTRAVENOUS TO ORAL SOLITHROMYCIN (CEM-101) COMPARED TO INTRAVENOUS TO ORAL MOXIFLOXACIN IN THE TREATMENT OF ADULT PATIENTS WITH COMMUNITY-ACQUIRED BACTERIAL PNEUMONIA.

Intervention/treatment:
SOLITHROMYCIN (CEM-101)
Medical condition:
PNEUMONIA
Protocol code:
CE01-301
Control number:
170088
Status:
Closed
Approved:
December 06, 2013
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT01968733
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Sponsor
CEMPRA PHARMACEUTICALS INC

Locations

Alberta

Edmonton, Alberta, T6G2B7

British Columbia

Surrey, British Columbia, V3V 1Z2
Vancouver, British Columbia, V6Z 1Y6

Manitoba

Winnipeg, Manitoba, R3E0J9

Quebec

Chicoutimi, Quebec, G7H5H6
Greenfield Park, Quebec, J4V2H1
Montreal, Quebec, H2W 1T8
Sherbrooke, Quebec, JIH-5N4
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