A Study of PTX-200 (Triciribine) Plus Cytarabine in Refractory or Relapsed Acute Leukemia

  • STATUS
    Recruiting
  • participants needed
    40
  • sponsor
    Prescient Therapeutics, Ltd.
Updated on 25 January 2022
chronic myeloid leukemia
myeloid leukemia
cytarabine
lymphocytic leukemia

Summary

A phase I-II open label study of PTX-200 in combination with cytarabine in the treatment of relapsed or refractory acute leukemia.

Description

Study design: Phase I/II study The Phase I study is open-label with four increasing dose levels for up to four 21-day cycles. Safety and activity will be evaluated at the end of each cycle.

The Phase II study is open label with administration of the recommended phase dose of PTX-200 for up to four 21-day cycles. PTX-200 will be co-administered with cytarabine in both the Phase I and Phase II parts of the study.

Details
Condition Acute Leukemia, acute leukemias
Treatment cytarabine, PTX-200
Clinical Study IdentifierNCT02930109
SponsorPrescient Therapeutics, Ltd.
Last Modified on25 January 2022

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