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Completed Phase 3 Interventional Results available

Phase 3 Study to Evaluate Safety and Efficacy of Iclaprim Versus Vancomycin for ABSSSI: REVIVE-1

ClinicalTrials.gov ID: NCT02600611

Public ClinicalTrials.gov record NCT02600611. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 9:32 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomized, Double-blind, Multicenter Study to Evaluate the Safety and Efficacy of Intravenous Iclaprim Versus Vancomycin in the Treatment of ABSSSI: REVIVE-1

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02600611
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Motif Bio
Industry
Enrollment
600 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 1, 2015 (Actual)
Primary completion
Jan 30, 2017 (Actual)
Completion
Jan 30, 2017 (Actual)
Last update posted
Jun 19, 2018

2015 – 2017

United States locations

U.S. sites
16
U.S. states
8
U.S. cities
15
Facility City State ZIP Site status
California Buena Park California 90620 —
California La Mesa California 91942 —
California Long Beach California 90806 —
California Modesto California 95350-449 —
California Oceanside California 92056 —
California Torrance California 90503 —
District of Columbia Washington D.C. District of Columbia 20017 —
Florida DeLand Florida 32770-0834 —
Florida Miami Florida 33144 —
Indiana Indianapolis Indiana 46260 —
Nebraska Lincoln Nebraska 68510-2462 —
Tennessee Franklin Tennessee 37067 —
Tennessee Franklin Tennessee 37094 —
Texas Channelview Texas 77530 —
Texas McAllen Texas 78503 —
Washington Seattle Washington 98195 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 40 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02600611, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 19, 2018 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02600611 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →