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Completed Phase 1 Interventional

A Study of Escalating Doses of ASG-22CE Given as Monotherapy in Subjects With Metastatic Urothelial Cancer and Other Malignant Solid Tumors That Express Nectin-4

ClinicalTrials.gov ID: NCT02091999

Public ClinicalTrials.gov record NCT02091999. 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 May 8, 2026, 4:51 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 1 Study of the Safety and Pharmacokinetics of Escalating Doses of ASG-22CE Given as Monotherapy in Subjects With Metastatic Urothelial Cancer and Other Malignant Solid Tumors That Express Nectin-4

Study identification

NCT ID
NCT02091999
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Astellas Pharma Global Development, Inc.
Industry
Enrollment
213 participants

Conditions and interventions

Interventions

  • enfortumab vedotin 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
May 13, 2014
Primary completion
Dec 6, 2022
Completion
Dec 6, 2022
Last update posted
Oct 31, 2024

2014 – 2022

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Site US00012 Los Angeles California 90033
Site US00019 Stanford California 94305
Site US00017 Aurora Colorado 80045
Site US00006 New Haven Connecticut 06520
Site US00007 Miami Florida 33136
Site US00008 Tampa Florida 33612
Site US00004 Fairway Kansas 66205
Site US00005 Ann Arbor Michigan 48109
Site US00003 Detroit Michigan 48201
Site US00021 Las Vegas Nevada 89119
Site US00018 New York New York 10029
Site US00002 New York New York 10065
Site US00023 Chapel Hill North Carolina 27599
Site US00013 Philadelphia Pennsylvania 19111
Site US00020 Pittsburgh Pennsylvania 15232
Site US00024 Fairfax Virginia 22031
Site US00009 Madison Wisconsin 53792
Site US00015 Milwaukee Wisconsin 53226

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02091999, 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 Oct 31, 2024 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02091999 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →