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Terminated Phase 2 Interventional

A Study of the CDX-1307 Vaccine Regimen in Patients With Newly Diagnosed Muscle-Invasive Bladder Cancer (The "N-ABLE" Study)

ClinicalTrials.gov ID: NCT01094496

Public ClinicalTrials.gov record NCT01094496. 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 Sep 2, 2026, 1:40 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 II, Open-Label Study of the CDX-1307 Vaccine Regimen as Neoadjuvant and Adjuvant Therapy in Patients With Newly Diagnosed Muscle-Invasive Bladder Cancer Expressing hCG-β

Brief summary

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

The major purpose of this study is to examine the anti-tumor activity of the CDX-1307 vaccine regimen when it is given before and after bladder cancer surgery. The study will also provide information about the safety of the vaccine regimen when given in combination with chemotherapy, and how it affects the immune systems.

Study identification

NCT ID
NCT01094496
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celldex Therapeutics
Industry
Enrollment
3 participants

Conditions and interventions

Conditions

Interventions

Biological · 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
Mar 31, 2010
Primary completion
Jun 30, 2011
Completion
Jun 30, 2011
Last update posted
Feb 12, 2020

2010 – 2011

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
BCG Oncology, PC Phoenix Arizona 85032
University of California - San Diego La Jolla California 92093
University of Southern California Norris Comprehensive Cancer Center LA-USC Medical Center Los Angeles California 90033
University of Colorado Cancer Center Aurora Colorado 80045
University of Florida Gainesville Florida 32610
Moffitt Cancer Center Tampa Florida 33612
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
University of Kentucky Markey Cancer Center Clinical Research Organization Lexington Kentucky 40536-0093
University of Maryland Greenebaum Cancer Center Baltimore Maryland 21201
Henry Ford Health System Detroit Michigan 48202
Washington University School of Medicine St Louis Missouri 63110
Roswell Park Cancer Center Buffalo New York 14263
Weill Cornell Medical College New York New York 10021
University of Rochester Rochester New York 14642
SUNY Upstate Medical University Syracuse New York 13210
Syracuse VA Medical Center Syracuse New York 13210
Thomas Jefferson University Philadelphia Pennsylvania 19107

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01094496, 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 Feb 12, 2020 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01094496 live on ClinicalTrials.gov.

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