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COMPLETED
NCT01242072
PHASE1

Intravenous Palifosfamide-tris in Combination With Etoposide and Carboplatin in Patients With Malignancies

Sponsor: Alaunos Therapeutics

View on ClinicalTrials.gov

Summary

This an an open-label study to define the safety profile and the maximum tolerated dose and confirm the clinical effective dose of palifosfamide-tris given intravenously in combination with etoposide and carboplatin in a wide range of cancers which etoposide and carboplatin are normally given. Once the maximum dose of palifosfamide-tris is determined,a Phase II study using the 3 agents combined will begin.

Official title: A Phase I Study of Intravenous (IV) Palifosfamide-tris Administered in Combination With IV Etoposide and IV Carboplatin in Patients With Malignancies for Which Etoposide and Carboplatin Are an Appropriate Choice

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

22

Start Date

2010-12

Completion Date

2012-07-16

Last Updated

2026-09-29

Healthy Volunteers

No

Interventions

DRUG

palifosfamide-tris

Intravenous on days 1, 2 and 3 of each 21-day cycle for up to 4 cycles

Locations (4)

Indiana University Simon Cancer Center

Indianapolis, Indiana, United States

Horizon Oncology Research

Lafayette, Indiana, United States

Medical Consultants, PC

Muncie, Indiana, United States

Washington University

St Louis, Missouri, United States