Last updated: 11/07/2018 13:25:56

An Open, Non-Comparative Multicenter Study to Assess the Efficacy and Safety of Oral Augmentin SR 2000/125 mg Twice Daily for 7 days for the Treatment of Bacterial Community-Acquired Pneumonia in adults.

GSK study ID
25000/547
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: An Open, Non-Comparative Multicenter Study to Assess the Efficacy and Safety of Oral Augmentin SR 2000/125 mg Twice Daily for 7 days for the Treatment of Bacterial Community-Acquired Pneumonia in adults.
Trial description: An Open, Non-Comparative Multicenter Study to Assess the Efficacy and Safety of Oral Augmentin SR 2000/125 mg Twice Daily for 7 days for the Treatment of Bacterial Community-Acquired Pneumonia in adults.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Bhatt K, Kalia V, Berkowitz E, Twynholm M, Abraham-van Parijs B, Hodge R. Efficacy and safety of pharmacokinetically enhanced amoxicillin/clavulanate 2000/125 mg (PKE AMX/CA) in patients with community-acquired pneumonia (CAP), including cases caused by penicillin-resistant S. pneumoniae. Abstracts from the 15th European Congress of Clinical Microbiology and Infectious Diseases, April 2005.
File T, Garau J, Jacobs MR, Wynne B, Berkowitz E, Twynholm M. Pharmacokinetically enhanced amoxicillin/clavulanate 2000/125 mg in the treatment of community-acquired pneumonia (CAP) caused by Streptococcus pneumoniae, including penicillin-resistant strains. Int J Antimicrob Agents 2005; 25(2):110119.
File T, Garau J, Jacobs MR, Wynne B. 2003. Pharmacokinetically enhanced amoxicillin/clavulanate 2000/125 mg in the treatment of community-acquired pneumonia (CAP) caused by Streptococcus pneumoniae, including penicillin-resistant strains. 41st Annual Meeting of the Infectious Disease Society of America, San Francisco, USA. Abstract 303.
File T, Jacobs MR, Poole MD, Wynne B. Clinical efficacy of pharmacokinetically enhanced amoxicillin/clavulanate (AMX/CA) vs comparators against Streptococcus pneumoniae (Sp) in respiratory tract infections (RTIs). Abstracts from the 2nd Forum on Respiratory Tract Infections, Monte Carlo, Monaco. February 2002, page 62, Abstract P4.
File T, Jacobs MR, Poole MD, Wynne B. Pharmacokinetically enhanced amoxicillin/clavulanate against Streptococcus pneumoniae (Sp) in respiratory tract infections (RTIs). Abstracts from the 42nd Interscience Conference on Antimicrobial Agents and Chemotherapy, San Diego, USA. September 2002, page 359, Abstract L-990.
Garau J, File T, Jacobs MR, Poole MD, Wynne B, The 546551, 566, 557 and 592 Clinical Study Groups. Efficacy of amoxicillin/clavulanate (AMX/CA) 2000/125 mg b.i.d. against Streptococcus pneumoniae non-susceptible to AMX. Abstracts from the 4th International Meeting on the Therapy of Infections, Florence, Italy. October 2002, page 71, Abstract A5.
Garau J, Jacobs MR, Wynne B, Berkowitz E, Twynholm M. Pharmacokinetically enhanced amoxicillin/clavulanate (AMX/CA) 2000/125 mg in the treatment of community-acquired pneumonia (CAP) and acute bacterial sinusitis (ABS) caused by Streptococcus pneumoniae. Abstracts from the 43rd Interscience Conference on Antimicrobial Agents and Chemotherapy. Chicago, USA. September 2003, page 422, Abstract L-1382.
Garau J. 2004. Performance in practice: bacteriological efficacy in patients with drug-resistant S. pneumoniae. Clin Microbiol Infect. 10(suppl. 2): 28-35.
S. Miller, M. Twynholm, E. Berkowitz, S. Gormley, A. White, L.A. Miller, C. Jakielaszek. Bacteriological outcomes with pharmacokinetically enhanced amoxicillin/clavulanate (2000/125 mg) in patients with community-acquired respiratory infection caused by Streptococcus pneumoniae, including drug-resistant (DRSP) strains. Abstracts from the 15th European Congress of Clinical Microbiology and Infectious Diseases, April 2005.
Thomas M, File T, Jacobs MR, Poole MD, Wynne B. 2002. Outcome of treatment of respiratory tract infections due to Streptococcus pneumoniae, including drug-resistant strains, with pharmacokinetically enhanced amoxicillin/clavulanate. Int J Antimicrob Agents 20(4):235-47.
Medical condition
Pneumonia, Community-Acquired
Product
amoxicillin/clavulanic acid
Collaborators
Not applicable
Study date(s)
November 1999 to November 2003
Type
Not applicable
Phase
3

Participation criteria

Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable

Trial location(s)

This study does not involve prospective enrollment of participants.

Study documents

Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English

If you wish to request for full study report, please contact - [email protected]

Results overview

Not applicable

Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2003-21-11

Plain language summaries

Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

Additional information about the trial

Not applicable
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