- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00424190
Comparative Study of Ceftaroline vs. Vancomycin Plus Aztreonam in Adult Subjects With Complicated Skin Infections (cSSSI)
A Phase 3, Multicenter, Randomized, Double-blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline Versus Vancomycin Plus Aztreonam in Adult Subjects With Complicated Skin and Skin Structure Infection
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Phase 3
Contacts and Locations
Study Locations
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Buenos Aires, Argentina
- Invetigational Site
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Buenos Aires, Argentina, 164
- Investigational Site
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Buenos Aires, Argentina
- Investigational Site
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Ciudad Autónoma de Buenos Aires, Argentina, 1240 C1180AAX
- Investigational Site
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Cordoba, Argentina
- Investigational Site
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Cordoba, Argentina
- Invetigational Site
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Entre Rios, Argentina
- Investigational Site
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Santa Fe, Argentina
- Investigational Site
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Curiuba-Parans, Brazil, 1089
- Investigational Site
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Sao Paulo, Brazil, 04039-020
- Investigational Site
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Santiago, Chile
- Investigational Site
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Vina del Mar, Chile
- Investigational Site
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Berlin, Germany, D-10249
- Investigational Site
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Bochum, Germany, 44791
- Investigational Site
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Hanau, Germany
- Investigational Site
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Plauen, Germany, 08529
- Investigational Site
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Quedlinburg, Germany, 06484
- Investigational Site
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Chihuahua, Mexico, 31238
- Investigational Site
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Lima, Peru, 29
- Invetigational Site
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Bytom, Poland, 41-902
- Investigational Site
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Krakow, Poland, 31-913
- Investigational Site
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Lublin, Poland, 20-081
- Investigational Site
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Sosnowiec, Poland, 41-200
- Investigational Site
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Todz, Poland, 91-425
- Investigational Site
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Bucharest, Romania, 010816
- Investigational Site
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Bucharest, Romania, 041915
- Investigational Site
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Timisoara, Romania, 300736
- Investigational Site
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Moscow, Russian Federation, 129327
- Investigational Site
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Moscow, Russian Federation, 105229
- Investigational Site
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Moscow, Russian Federation, 111539
- Investigational Site
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Smolensk, Russian Federation, 214019
- Investigational Site
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St. Petersburg, Russian Federation, 194354
- Investigational Site
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St. Petersburg, Russian Federation, 192242
- Investigational Site
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St. Petersburg, Russian Federation, 196247
- Investigational Site
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Dnipropetrovsk, Ukraine, 49600
- Investigational Site
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Ivano-Frankivsk, Ukraine, 76008
- Investigational Site
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Lviv, Ukraine, 79659
- Investigational Site
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Alabama
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Dothan, Alabama, United States, 36301
- Investigational Site
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California
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Long Beach, California, United States, 90813
- Investigational Site
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Los Angeles, California, United States, 90015
- Investigational Site
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Sacramento, California, United States, 95817
- Investigational Site
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Sacramento, California, United States, 95819
- Investigational Site
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San Diego, California, United States, 92114
- Investigational Site
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San Francisco, California, United States, 94110
- Investigational Site
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Torrance, California, United States, 90509
- Investigational Site
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Georgia
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Savannah, Georgia, United States, 31405
- Investigational Site
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Illinois
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Naperville, Illinois, United States, 60540
- Investigational Site
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Indiana
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Indianapolis, Indiana, United States, 46280
- Investigational Site
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Louisiana
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Shreveport, Louisiana, United States, 71103
- Investigational Site
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Ohio
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Columbus, Ohio, United States, 43215
- Investigational Site
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Pennsylvania
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Landsdale, Pennsylvania, United States, 19446
- Investigational Site
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Washington
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Tacoma, Washington, United States, 98405
- Investigational Site
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Skin and skin structure infection (SSSI) that involves deeper soft tissue or requires significant surgical intervention, or cellulitis or abscess on lower extremity which occurs in subjects with diabetes mellitus or well-documented peripheral vascular disease.
Exclusion Criteria:
- Prior treatment of current cSSSI with an antimicrobial.
- Failure of vancomycin or aztreonam as therapy for the current cSSSI, or prior isolation of an organism with in vitro resistance to vancomycin or aztreonam.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Ceftaroline for Injection
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600 mg parenteral infused over 60 minutes, every 12 hours for 5 to 14 days
Other Names:
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Active Comparator: IV Vancomycin and IV Aztreonam
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vancomycin at 1 g parenteral infused over 60 minutes followed by aztreonam 1 g infused over 60 minutes, every 12 hours, for 5 to 14 days.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Clinical Cure Rate at Test of Cure (TOC) (MITT Population)
Time Frame: 8-15 days after the end of treatment
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Cure: Total resolution of all signs and symptoms of the baseline infection, or improvement of the infection such that no further antimicrobial therapy was necessary. Failure: Requirement of alternative antimicrobial therapy for primary infection of cSSSI due to inadequate response, recurrence, new infection at the same site; treatment-limiting adverse event (AE); requirement for surgery due to failure of study drug; diagnosis of osteomyelitis after Study Day 8; or death caused by cSSSI. Indeterminate: Inability to determine an outcome |
8-15 days after the end of treatment
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Clinical Cure Rate of Ceftaroline Compared With That of Vancomycin Plus Aztreonam Treatment at TOC in the Clinically Evaluable (CE) Population
Time Frame: 8-15 days after last dose of study drug
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8-15 days after last dose of study drug
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Microbiological Success Rate at the TOC Visit
Time Frame: 8-15 days after last dose of study drug
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8-15 days after last dose of study drug
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Clinical Response at the End of Therapy (EOT) Visit
Time Frame: Last day of study drug administration
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Last day of study drug administration
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Clinical and Microbiological Response by Pathogen at the TOC Visit
Time Frame: 8-15 days after last dose of study drug
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8-15 days after last dose of study drug
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Clinical Relapse at the Late Follow Up (LFU) Visit
Time Frame: 21 to 35 days after the last dose of study drug
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21 to 35 days after the last dose of study drug
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Microbiological Reinfection or Recurrence at the LFU Visit
Time Frame: 21 to 35 days after the last dose of study drug
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21 to 35 days after the last dose of study drug
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Assess Safety
Time Frame: First dose of study drug through TOC visit
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Comparisons of the number of participants with Adverse Events
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First dose of study drug through TOC visit
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ralph Corey, MD, Duke University
Publications and helpful links
General Publications
- Dryden M, Kantecki M, Yan JL, Stone GG, Leister-Tebbe H, Wilcox M. Treatment outcomes of secondary bacteraemia in patients treated with ceftaroline fosamil: pooled results from six phase III clinical trials. J Glob Antimicrob Resist. 2022 Mar;28:108-114. doi: 10.1016/j.jgar.2021.10.027. Epub 2021 Dec 16.
- Cheng K, Pypstra R, Yan JL, Hammond J. Summary of the safety and tolerability of two treatment regimens of ceftaroline fosamil: 600 mg every 8 h versus 600 mg every 12 h. J Antimicrob Chemother. 2019 Apr 1;74(4):1086-1091. doi: 10.1093/jac/dky519.
- Wilcox M, Yan JL, Gonzalez PL, Dryden M, Stone GG, Kantecki M. Impact of Underlying Comorbidities on Outcomes of Patients Treated with Ceftaroline Fosamil for Complicated Skin and Soft Tissue Infections: Pooled Results from Three Phase III Randomized Clinical Trials. Infect Dis Ther. 2022 Feb;11(1):217-230. doi: 10.1007/s40121-021-00557-w. Epub 2021 Nov 6.
- Corey GR, Wilcox MH, Gonzalez J, Jandourek A, Wilson DJ, Friedland HD, Das S, Iaconis J, Dryden M. Ceftaroline fosamil therapy in patients with acute bacterial skin and skin-structure infections with systemic inflammatory signs: A retrospective dose comparison across three pivotal trials. Int J Antimicrob Agents. 2019 Jun;53(6):830-837. doi: 10.1016/j.ijantimicag.2019.01.016. Epub 2019 Feb 1.
- Corrado ML. Integrated safety summary of CANVAS 1 and 2 trials: Phase III, randomized, double-blind studies evaluating ceftaroline fosamil for the treatment of patients with complicated skin and skin structure infections. J Antimicrob Chemother. 2010 Nov;65 Suppl 4:iv67-iv71. doi: 10.1093/jac/dkq256.
- Corey GR, Wilcox MH, Talbot GH, Thye D, Friedland D, Baculik T; CANVAS 1 investigators. CANVAS 1: the first Phase III, randomized, double-blind study evaluating ceftaroline fosamil for the treatment of patients with complicated skin and skin structure infections. J Antimicrob Chemother. 2010 Nov;65 Suppl 4:iv41-51. doi: 10.1093/jac/dkq254.
- Corey GR, Wilcox M, Talbot GH, Friedland HD, Baculik T, Witherell GW, Critchley I, Das AF, Thye D. Integrated analysis of CANVAS 1 and 2: phase 3, multicenter, randomized, double-blind studies to evaluate the safety and efficacy of ceftaroline versus vancomycin plus aztreonam in complicated skin and skin-structure infection. Clin Infect Dis. 2010 Sep 15;51(6):641-50. doi: 10.1086/655827.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
- Ceftaroline
- Abscess
- cSSSI
- Staphylococcus aureus
- Antibiotic
- Cephalosporin
- Intravenous
- Prodrug
- Surgical site infection
- Cellulitis
- Antimicrobial
- Skin infection
- Antibacterial
- Bacterial infection, skin
- Ceftaroline acetate
- Complicated skin and skin structure infection
- Methicillin-resistant Staphylococcus Aureus (MRSA)
- PPI-0903
- Skin disease, bacterial
- Staphylococcal skin infection
- Streptococcal skin infection
- TAK-599
Additional Relevant MeSH Terms
Other Study ID Numbers
- P903-06
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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