Skip to main content
Clinical Trials/NCT00064376
NCT00064376
Completed
Phase 2

A Phase II Trial Of Paricalcitol In Myelodysplastic Syndromes

Cedars-Sinai Medical Center1 site in 1 countryMay 2003

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Leukemia
Sponsor
Cedars-Sinai Medical Center
Locations
1
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

RATIONALE: Paricalcitol is a form of vitamin D that may help myelodysplastic cells develop into normal bone marrow cells.

PURPOSE: Phase II trial to study the effectiveness of paricalcitol in treating patients who have myelodysplastic syndrome.

Detailed Description

OBJECTIVES: * Determine the clinical effects of paricalcitol in patients with myelodysplastic syndromes. * Determine whether this drug can improve RBC, WBC, or platelet counts in these patients. * Determine whether this drug can decrease the risk of development of leukemia without causing undue toxicity in these patients. OUTLINE: Patients receive oral paricalcitol daily for 4 months in the absence of disease progression or unacceptable toxicity. Patients are followed at 1 month. PROJECTED ACCRUAL: A total of 20 patients will be accrued for this study within 8 months.

Registry
clinicaltrials.gov
Start Date
May 2003
End Date
November 2005
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

H. Phillip Koeffler

Director, Medicine / Hematology/Oncology

Cedars-Sinai Medical Center

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

Loading locations...

Similar Trials