A Phase III Study of Faropenem in the Treatment of Adult Community-acquired Bacterial Pneumonia

Phase 3

• Conditions: Community Acquired Pneumonia
• Interventions: Drug: Faropenem; Drug: Ertapenem

• Registration Number: NCT01937832
• Lead Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Brief Summary

The purpose of this study is to evaluate the safety and Efficacy of Faropenem in community-acquired pneumonia (CAP) subjects

Detailed Description

Not available

Study Timeline

• Status Verified: 2013-09
• Study First Submitted: 2013-09-04
• Study First Submitted QC: 2013-09-04
• Last Update Submitted: 2013-09-04
• Study First Posted: 2013-09-10
• Last Update Posted: 2013-09-10
• Study Start: 2013-10
• Primary Completion: 2015-10

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 540

Inclusion Criteria

1. Patients aged between18~73 years, either male or female
2. Patients requiring hospitalization or emergency room observation, and the need to receive intravenous antibiotic treatment
3. Women of childbearing age having negative pregnancy test at the time of enrollment and agreeing to take effective contraceptive measures from the delivery to 7 ~14 days after stopping .(for example: oral contraception, injectable contraception, or implant contraception , spermicides and condoms, or IUDs).
4. Comply with the following clinical, radiological and microbiological criteria of Community-Acquired Pneumonia(CAP)
5. Patients had used ineffective systemic antimicrobial drugs before enrollment or had effective antimicrobial drugs within 72h before enrollment, used <24h
6. Informed consent granted

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Exclusion Criteria

1. Patients with atypical pneumonia infected by the Mycoplasma pneumoniae, Chlamydia pneumoniae, Legionella pneumophila bacteria;
2. Patients infected by pathogens MRSA, Pseudomonas aeruginosa or Acinetobacter baumannii;
3. Viral pneumonia;
4. Aspiration pneumonia;
5. Hospital-acquired pneumonia, including ventilator-associated pneumonia;
6. Patients with Severe pneumonia who meet one primary criterion or three secondary criteria (See Appendix);
7. Patients with a rapid progressive or end-stage disease, and can not survive until the end of the study period by antibiotic treatment;
8. Patients with bronchial obstruction or a history of obstructive pneumonia (not including chronic obstructive pulmonary disease);
9. Suffering from any of the following diseases: active tuberculosis, bronchiectasis, lung abscess, lung cancer, non-infectious interstitial lung disease, pulmonary edema, atelectasis, pulmonary embolism, pulmonary eosinophil infiltration disease and pulmonary vasculitis;
10. Infections acquired from hospitals, nursing homes or other long-term care facilities, or patients hospitalized within 14 days prior to enrollment ;
11. Allergic to penem and carbapenem antibiotic;
12. Pregnancy or lactation in women;
13. Patients with uncontrolled psychiatric history or those at risk of suicide two years prior to enrollment;
14. A history of epilepsy or other central nervous system disorders in patients;
15. Patients with Renal dysfunction, screening serum creatinine values above the upper limit of normal 10%;
16. The Screening alanine aminotransferase (ALT) or aspartate aminotransferase (AST) is 3 times the upper limit of the reference value, or total bilirubin beyond the upper limit of the normal range by 10% ;
17. Serious diseases that affecting the immune system, such as: a human immunodeficiency virus (HIV) infection history, or CD4 + T-lymphocyte count <200/200/mm3, or Neutrophilic granulocytopenia (neutrophil count <1500/mm3), or hematologic malignancies or solid organ or splenectomy, etc;
18. Patients who are taking steroid medications, at least 20mg daily dose of prednisone(or equivalent doses of other glucocorticoids);
19. Patients who are accepting chemotherapy drug therapy or anti-cancer therapy, or plan to accept such treatment during the trial six months prior to enrollment;
20. Alcohol or illicit drug abuse history;
21. Patients who have accepted any other experimental drugs within 3 months prior to enrollment;
22. more than 500ml blood donation within 3 months prior to enrollment;
23. Patients who have participated in this clinical trial ever before;
24. Combined use of other antibacterial drugs in patients;
25. Patients are diagnosed to have potential increased risks, or there may be interference with clinical trials;

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Faropenem	Faropenem	-
Ertapenem	Ertapenem	-

Primary Outcome Measures

Name	Time	Method
Per subject clinical cure rate	7-14 days

Trial Locations

Locations (7)

The Second Hospital of Jilin University; 🇨🇳 Changchun, Jilin, China

The Third Affiliated Hospital of Sun Yat-sen University; 🇨🇳 Guangzhou, Guangdong, China

Anhui Provincial Hospital; 🇨🇳 Hefei, Anhui, China

Taihe Hospital in Shiyan City; 🇨🇳 Shiyan, Hubei, China

Qingdao Municipal Hospital; 🇨🇳 Qingdao, Shandong, China

Huashan Hospital ,Fudan University; 🇨🇳 Shanghai, China

The Second Hospital of Tianjin Medical University; 🇨🇳 Tianjin, China