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A Study to Evaluate PT-523 in Patients With Refractory Leukemia

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Spectrum Pharmaceuticals

Status and phase

Withdrawn
Phase 2
Phase 1

Conditions

Leukemia

Treatments

Drug: PT-523 for Injection

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

This Phase I/II, multi-centered, non-randomized, trial is designed to determine a safe dose of PT-523 for subjects, and to make preliminary evaluations on the activity of PT-523 as therapy in subjects with refractory leukemia.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Relapsed/refractory leukemias including acute non-lymphocytic leukemia (AML), acute lymphocytic leukemia (ALL), chronic lymphocytic leukemia (CLL), and chronic myelogenous leukemia in blastic phase (CML-BP) for which no standard therapies are anticipated to result in a durable remission; or poor-risk myelodysplasia (MDS) patients to include refractory anemia with excess blasts (RAEB) or excess blasts in transformation (RAEBT) and chronic myelomonocytic leukemia (CMML) who are either relapsed/refractory or who refuse/are not eligible for frontline therapy.
  • Only patients with refractory ALL or CML in lymphoid blastic phase are eligible for phase II.
  • ECOG performance status 0 - 2.
  • Adequate organ function and bone marrow reserve.
  • At least 4 weeks must have elapsed from the time of major surgery.
  • Use of appropriate contraceptive method.
  • Signed patient informed consent.

Exclusion criteria

  • Known human immunodeficiency virus (HIV).
  • Active heart disease including myocardial infarction within previous 3 months, symptomatic coronary artery disease, arrhythmias not controlled by medication, or uncontrolled congestive heart failure.
  • Patients receiving any other standard or investigational treatment for their leukemia other than corticosteriods, hydroxyurea, and 6-mercaptopurine.
  • Any medical condition which, in the opinion of the investigator, places the patient at an unacceptably high risk for toxicities.

Trial contacts and locations

6

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Data sourced from clinicaltrials.gov

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