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Terminated Phase 2 Interventional Results available

Adenoviral Vector Monotherapy or Combination With Chemotherapy in Subjects With Recurrent/Metastatic Breast Cancer.

ClinicalTrials.gov ID: NCT01703754

Public ClinicalTrials.gov record NCT01703754. 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 23, 2026, 6:18 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 Randomized, Open Label Study of Ad-RTS-hIL-12 Monotherapy or Combination With Palifosfamide in Subjects With Recurrent/Metastatic Breast Cancer and Accessible Lesions

Brief summary

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

Phase II, randomized, safety and efficacy study in recurrent/metastatic breast cancer with accessible lesions. Primary End point is rate of Progression Free Survival (PFS) at the 16 week treatment time point. Hypothesis: Adenoviral vector (Ad-RTS-hIL-12) alone and in combination with chemotherapy (palifosfamide) is safe and efficacious.

Study identification

NCT ID
NCT01703754
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alaunos Therapeutics
Industry
Enrollment
12 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
Apr 4, 2013 (Actual)
Primary completion
Aug 7, 2014 (Actual)
Completion
Aug 7, 2014 (Actual)
Last update posted
Aug 28, 2025

2013 – 2014

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Baptist Cancer Institute Jacksonville Florida 32207 —
Henry Ford Health System Detroit Michigan 48202 —
Billings Clinic Billings Montana 59101 —
Signal Point Clinical Research Center Middletown Ohio 45042 —
Greenville Hospital System Greenville South Carolina 29605 —
The Jones Clinic, PC Germantown Tennessee 38138 —
Mary Crowley Medical Research Center Dallas Texas 75201 —
Evergreen Hematology & Oncology Spokane Washington 99218 —

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 NCT01703754, 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 Aug 28, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01703754 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →