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Completed

NCT Number: NCT01529476

Study to Evaluate the Efficacy and Safety of Oral Administration With Nemonoxacin and Levofloxacin in Patients With CAP

1. This study will test the safety and efficacy of TG-873870 (Nemonoxacin) compared with Levofloxacin in adult patients with Community-Aquired Pneumonia (CAP) 2. To investigate the population pharmacokinetics (PPK) of nemonoxacin in adult patients with CAP after continuous oral administration and determine the pharmacokinetic (PK)/pharmacodynamic (PD).

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Anzhen Hospital,Beijing Capital Medical University, Anzhen, China

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About this study

Community-acquired Pneumonia (CAP) remains a leading cause of death in both developing and developed countries. In the choice of antibacterial agents used to treat CAP, fluoroquinolones have received considerable attention because of their wide spectrum of bactericidal activity. TG-873870 (Nemonoxacin), a non-fluorinated quinolone (NFQ), is a selective bacterial topoisomerase inhibitor. This study will test the safety and efficacy of TG-873870 (Nemonoxacin) compared with Levofloxacin in adult patients with Community-Aquired Pneumonia (CAP).

Besides,the population pharmacokinetics (PPK) of nemonoxacin in adult patients with CAP after continuous oral administration and determine the pharmacokinetic (PK)/pharmacodynamic (PD).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ages between 18 and 70;
  • Weighs between 40 ~ 100 kg, and BMI ≥ 18 kg/m2;
  • Must have a clinical diagnosis of CAP
  • Chest X-ray shows new or persist/progressive infiltrates
  • If female, non-lactating and at no risk or pregnancy (post-menopausal or must use adequate birth control)
  • The patient is able to take the drug orally.

Exclusion criteria

  • Patients with CAP that, in the investigator's judgment, is severe enough to require hospitalization for intravenous antibiotic therapy and/or supplemental oxygen therapy with ICU support
  • Known or suspected severe bronchiectasis, cystic fibrosis, active pulmonary tuberculosis or infection with other mycobacteria or fungi, known bronchial obstruction, a history of post-obstructive pneumonia, other confounding respiratory diseases, such as lung cancer, malignancy metastatic to the lungs, lung abscess, empyema, suspected aspiration pneumonia due to vomiting, or non-bacterial respiratory infection (chronic obstructive pulmonary disease [COPD] is not exclusionary)
  • Clinically significant conduction or other abnormality on 12-lead ECG, or QTc interval
  • Potassium is < 3.5 mmol/L
  • Any known disease that seriously affect the immune system
  • Active hepatitis or decompensated cirrhosis;
  • Have used quinolones or fluoroquinolones within 14 days before enrollment
  • Patients who are being or will be on a long-term medication of steroids

Treatment and study plan

Levofloxacin

Drug

levofloxacin 500 mg,QD,7~10 days

Nemonoxacin

Drug

Nemonoxacin 500mg,QD,7~10 days

Primary outcomes

  1. Per subject clinical cure rate

    Time frame: 21days

    The clinical cure rate will be evaluated according to signs and symptoms and changes in the chest X-ray.

Secondary outcomes

  1. Safety Evaluation

    Time frame: 24days

    Clinical adverse events and abnormal laboratory or other special test findings during this study should be observed and recorded carefully.

  2. Per subject microbiological cure rate

    Time frame: 14 days

    The microbiological cure rate will be evaluated according to the microbiological identification results of the central laboratory

  3. Per subject overall cure rate

    Time frame: 14 days

    Evaluate the overall efficacy after a comprehensive consideration of the clinical results and the bacteriological results.

Sponsors and collaborators

Lead sponsor

TaiGen Biotechnology Co., Ltd.

Industry

Collaborators

  • PPD Development, LP
  • Parexel
  • Qualitix Clinical Research Co., Ltd.

Registry information

Official study title

A Randomized, Double-Blind, Comparative, Multi-Center Study of the Safety and Efficacy of TG-873870(Nemonoxacin) Versus Levofloxacin in Adult Patients With Community-Acquired Pneumonia (CAP)

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Feb 8, 2012
Registry last updated
Jun 18, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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