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Completed Phase 2 Interventional Results available

CD101 Compared to Caspofungin Followed by Oral Step Down in Subjects With Candidemia and/or Invasive Candidiasis-Bridging Extension

ClinicalTrials.gov ID: NCT02734862

Public ClinicalTrials.gov record NCT02734862. 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 Jul 21, 2026, 6:45 PM 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 2, Multicenter, Randomized, Double-blind Study of the Safety, Tolerability, and Efficacy of Intravenous CD101 vs Intravenous Caspofungin Followed by Oral Fluconazole Step-down in the Treatment of Subjects With Candidemia and/or Invasive Candidiasis

Study identification

NCT ID
NCT02734862
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cidara Therapeutics Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
Industry
Enrollment
207 participants

Conditions and interventions

Interventions

  • CD101 Drug
  • Caspofungin Drug
  • Fluconazole Drug
  • intravenous placebo Drug
  • oral placebo Drug

Drug

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
Jul 25, 2016
Primary completion
May 31, 2019
Completion
Jun 30, 2019
Last update posted
Dec 7, 2020

2016 – 2019

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233
University of California - Davis Davis California 95817
University of Miami Miller School of Medicine Miami Florida 33136
Augusta University Augusta Georgia 30912
Brigham and Women's Hospital Boston Massachusetts 02115
Harper University Hospital Detroit Michigan 48201
Henry Ford Health System Detroit Michigan 48202
William Beaumont Hospital Royal Oak Michigan 48073
University of Mississippi Medical Center Jackson Mississippi 39216
Washington University School of Medicine St Louis Missouri 63110
Mercury Street Medical Butte Montana 59701
Albany Medical Center Albany New York 12208
Mercy Health - St. Vincent Medical Center - ID Clinical Research Toledo Ohio 43608
Reading Hospital and Medical Center West Reading Pennsylvania 19611
University of Texas Health Science Center at Houston Houston Texas 77030
Virginia Tech, Carillion School of Medicine Roanoke Virginia 24016

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 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02734862, 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 Dec 7, 2020 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02734862 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →