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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 Oct 20, 2026, 6:34 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 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

Brief summary

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

The purpose of this study is to determine if intravenous CD101 is safe and effective in the treatment of candidemia and/or invasive candidiasis when compared to caspofungin (followed by oral fluconazole).

Study identification

NCT ID
NCT02734862
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
207 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
Jul 26, 2016 (Actual)
Primary completion
Jun 2019 (Actual)
Completion
Jul 2019 (Actual)
Last update posted
Dec 8, 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 8, 2020 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02734862 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →