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Clinical Trial Summary

This is a multicenter, randomized, double-blind study of the efficacy and safety of iclaprim compared to vancomycin for the treatment of skin and skin structure infections.


Clinical Trial Description

This is a multicenter, randomized, double-blind study of the efficacy and safety of IV iclaprim compared to IV vancomycin. Patients will receive either iclaprim or vancomycin for 5 to 14 days. Patients will be evaluated daily up to early time point (ETP), then every 48 to 72 hours through the end of treatment. Patients will also be evaluated at the test of cure (TOC) visit (7 to 14 days post-EOT), and will have a Late Follow-Up (LFU) visit (28 to 32 days post-first dose). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02607618
Study type Interventional
Source Motif Bio
Contact
Status Completed
Phase Phase 3
Start date November 2015
Completion date August 8, 2017

See also
  Status Clinical Trial Phase
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Completed NCT01984684 - Delafloxacin vs Vancomycin and Aztreonam for the Treatment of Acute Bacterial Skin and Skin Structure Infections Phase 3
Completed NCT02378480 - Omadacycline Versus Linezolid for the Treatment of ABSSSI (EudraCT #2013-003644-23) Phase 3
Withdrawn NCT00876850 - Phase 3 Study - Safety and Efficacy of PTK 0796 in Patients With Complicated Skin and Skin Structure Infection (CSSSI) Phase 3
Completed NCT02863874 - The PLUS Study: Comparison of VicrylPlus® Versus Vicryl® for Repair of Perineal Tears N/A
Completed NCT02877927 - Oral Omadacycline vs. Oral Linezolid for the Treatment of ABSSSI Phase 3