Study of Farnesyl Protein Transferase Inhibitor (FPTI) in Patients With Leukemia (Study P00701)(TERMINATED)

This study has been terminated.

First Received: May 1, 2002 Last Updated: May 31, 2006 History of Changes

Sponsored by:	Schering-Plough
Information provided by:	Schering-Plough
ClinicalTrials.gov Identifier:	NCT00034684

Purpose

The purpose of this study is to determine the safety and tolerability of an oral Farnesyl Protein Transferase Inhibitor (SCH 66336) as a single agent in patients with Advanced Myelodysplastic Syndrome, Acute Myelogenous Leukemia, Chronic Myelogenous Leukemia in Blast Crisis, or Acute Lymphoblastic Leukemia.

Condition	Intervention	Phase
Leukemia Myelodysplastic Syndromes Leukemia, Myeloid, Chronic Blast Crisis Leukemia, Lymphocytic	Drug: Farnesyl Protein Transferase Inhibitor	Phase I Phase II

Study Type:	Interventional
Study Design:	Treatment, Non-Randomized, Open Label, Dose Comparison, Parallel Assignment, Safety Study
Official Title:	Safety and Tolerability Study of Farnesyl Protein Transferase Inhibitor (FPTI) in Patients With Leukemia

Resource links provided by NLM:

MedlinePlus related topics: Leukemia, Adult Acute Leukemia, Adult Chronic

U.S. FDA Resources

Further study details as provided by Schering-Plough:

Estimated Enrollment:	90
Study Start Date:	June 2001
Estimated Study Completion Date:	March 2004

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Pathologically documented chronic myelogenous leukemia in blast crisis, myelodysplasia, acute myelogenous leukemia, or acute lymphocytic leukemia.
Life expectancy of 12 weeks or greater.
ECOG Performance Status less than or equal to 2.
Meets protocol requirements for specified laboratory values.
No manifestations of a malabsorption syndrome.

Exclusion Criteria:

Patients who have received more than three chemotherapy regimens for more than three recurrences of the disease.
Poor medical risks because of nonmalignant systemic disease as well as those with active uncontrolled conditions.
Patients who have received investigational therapy of any type within 30 days prior to administration.

Contacts and Locations

No Contacts or Locations Provided

More Information

No publications provided

Study ID Numbers:	P00701
Study First Received:	May 1, 2002
Last Updated:	May 31, 2006
ClinicalTrials.gov Identifier:	NCT00034684 History of Changes
Health Authority:	United States: Food and Drug Administration

Keywords provided by Schering-Plough:

Leukemia
Myelodysplastic Syndromes
Leukemia, Myeloid
Leukemia, Lymphocytic

Study placed in the following topic categories:

Blast Crisis
Leukemia, Lymphoid
Immunoproliferative Disorders
Precancerous Conditions
Hematologic Diseases
Myelodysplastic Syndromes
Myeloproliferative Disorders

Leukemia, Myeloid
Leukemia
Lymphatic Diseases
Preleukemia
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Bone Marrow Diseases
Lymphoproliferative Disorders

Additional relevant MeSH terms:

Blast Crisis
Leukemia, Lymphoid
Disease
Immunoproliferative Disorders
Neoplasms by Histologic Type
Precancerous Conditions
Immune System Diseases
Hematologic Diseases
Myelodysplastic Syndromes
Myeloproliferative Disorders
Leukemia, Myeloid

Lymphatic Diseases
Leukemia
Preleukemia
Neoplasms
Neoplastic Processes
Pathologic Processes
Syndrome
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Lymphoproliferative Disorders
Bone Marrow Diseases
Cell Transformation, Neoplastic

ClinicalTrials.gov processed this record on July 02, 2009