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Trial record 45 of 430 for:    ifosfamide

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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01242072
Recruitment Status : Unknown
Verified July 2012 by Ziopharm.
Recruitment status was:  Active, not recruiting
First Posted : November 16, 2010
Last Update Posted : July 18, 2012
Information provided by (Responsible Party):

Brief 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.

Condition or disease Intervention/treatment Phase
Malignancy Cancer Non Small Cell Lung Cancer Small Cell Lung Cancer Testicular Cancer Thymoma Ovarian Cancer Osteosarcoma Drug: palifosfamide-tris Phase 1

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 12 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
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
Study Start Date : November 2010
Estimated Primary Completion Date : December 2012
Estimated Study Completion Date : December 2012

Arm Intervention/treatment
Experimental: PaCE
Palifosfamide, Carboplatin and Etoposide
Drug: palifosfamide-tris
Intravenous on days 1, 2 and 3 of each 21-day cycle for up to 4 cycles

Primary Outcome Measures :
  1. Assess the safety profile [ Time Frame: 21 Days ]
    Adverse events, vital signs, physical examination, laboratory data and concomitant medications

Secondary Outcome Measures :
  1. Determine the maximum tolerated dose [ Time Frame: Up to 21 days ]
    Each dose level cohort will be 3 subjects. After 3 subjects have received a regimen, there will be a minimum observation period of 1 full cycle (21 days) for each of the 3 subjects before enrollment of the group of subjects at the next dose level.

  2. Assess early signs of efficacy [ Time Frame: duration of study ]
    To assess early signs of efficacy using this investigational combination in this patient population

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • 18 years old or greater
  • Malignancy scheduled to receive etoposide and carboplatin therapy
  • Eastern Cooperative Oncology Group (ECOG) performance of 0 or 1
  • Adequate bone marrow, liver, renal function and coagulation status
  • Informed consent
  • Agree to use birth control through 28 days of last treatment dose
  • Pregnancy test for women of child-bearing potential
  • No available standard therapy

Exclusion Criteria:

  • Allergy to the the study treatment drugs
  • Unstable current medical condition
  • Presence or history of injury to the urinary tract
  • Active infection
  • Major surgery within 4 weeks prior to treatment
  • Minor surgery within 2 weeks prior to treatment
  • Current acute steroid therapy or taper
  • Currently pregnant or nursing
  • Substance abuse or condition that may interfere with participation
  • Received other investigational drugs within 30 days
  • Within 4 weeks of their last chemotherapy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01242072

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United States, Indiana
Indiana University Simon Cancer Center
Indianapolis, Indiana, United States, 46202
Horizon Oncology Research
Lafayette, Indiana, United States, 47905
Medical Consultants, PC
Muncie, Indiana, United States, 47303
United States, Missouri
Washington University
St. Louis, Missouri, United States, 63110
Sponsors and Collaborators

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Responsible Party: Ziopharm Identifier: NCT01242072     History of Changes
Other Study ID Numbers: IPM1004
First Posted: November 16, 2010    Key Record Dates
Last Update Posted: July 18, 2012
Last Verified: July 2012

Keywords provided by Ziopharm:
etoposide and carboplatin
non small cell lung cancer
small cell lung cancer
testicular cancer
ovarian cancer

Additional relevant MeSH terms:
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Isophosphamide mustard
Lung Neoplasms
Carcinoma, Non-Small-Cell Lung
Ovarian Neoplasms
Carcinoma, Ovarian Epithelial
Small Cell Lung Carcinoma
Thymus Neoplasms
Testicular Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Lung Diseases
Respiratory Tract Diseases
Carcinoma, Bronchogenic
Bronchial Neoplasms
Endocrine Gland Neoplasms
Ovarian Diseases
Adnexal Diseases
Genital Diseases, Female
Genital Neoplasms, Female
Urogenital Neoplasms
Endocrine System Diseases
Gonadal Disorders
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type