Ceftazidime-Avibactam for the Treatment of Infections Due to Ceftazidime Resistant Pathogens



Status:Completed
Conditions:Infectious Disease, Urology
Therapuetic Areas:Immunology / Infectious Diseases, Nephrology / Urology
Healthy:No
Age Range:18 - 90
Updated:10/1/2017
Start Date:January 2013
End Date:September 2014

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An Open-Label, Randomized, Multicenter, Phase III Study of Ceftazidime Avibactam (CAZ-AVI, Formerly CAZ104) and Best Available Therapy for the Treatment of Infections Due to Ceftazidime Resistant Gram Negative Pathogens

To Evaluate the Effects of Ceftazidime-Avibactam and Best Available Therapy in patients with
complicated urinary tract infections and complicated intra-abdominal infections.

An Open-Label, Randomized, Multicenter, Phase III Study of Ceftazidime Avibactam (CAZ-AVI,
formerly CAZ104) and Best Available Therapy for the Treatment of Infections Due to
Ceftazidime Resistant Gram Negative Pathogens

Inclusion Criteria:

- Patient must be ≥18 and ≤90 years of age

- Female patients can participate if they are surgically sterile or completed menopause
or females capable of having children and agree not to attempt pregnancy while
receiving IV study therapy and for a period of 7 days after

- Patient has a ceftazidime-resistant Gram negative pathogen that was isolated from an
appropriate culture within 5 days prior to study entry (ie, within 5 days prior to
Screening; the study-qualifying culture), which was determined to be the causative
agent of the entry infection

Exclusion Criteria:

- Patient has an APACHE II score >30 (cIAI patients only)

- Patient has an infection due to Gram negative pathogen that is unlikely to respond to
CAZ-AVI treatment (eg, Acinetobacter spp., Stenotrophomonas spp.)

- Patient is receiving hemodialysis or peritoneal dialysis or had a renal transplant
Patient is immunocompromised

- Patient has a rapidly progressive or terminal illness with a high risk of mortality
due to any cause, including acute hepatic failure, respiratory failure or severe
septic shock such that they are unlikely to survive the 4- to 5-week study period.
We found this trial at
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El Talar,
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Lima, OH
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Shreveport, LA
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