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Alliance A041701

Trial Overview

Official Title

A Randomized Phase II/III Study of Conventional Chemotherapy +/- Uproleselan (GMI-1271) in Older Adults with Acute Myeloid Leukemia Receiving Intensive Induction Chemotherapy

Study Purpose

To compare the usual treatment alone to using uproleselan plus the usual treatment.

Diagnosis

Acute Myeloid Leukemia

Eligibility

No prior chemotherapy for MDS or AML

Patients must sign an approved informed consent and authorization permitting release of personal health information.

Intervention

  • Group 1: Daunorubicin + Cytarabine (usual approach group)
  • Group 2: Daunorubicin + Cytarabine + Uproleselan (study drug)

Patients will either get the usual treatment or the usual treatment plus the study drug for up to 5 months. After treatment is finished the doctor will continue to follow up and watch for side effects for up to 5 years.

For more information, visit the U.S. National Library of Medicine clinical trial database.

Key Participation Requirements
Trial Location(s)
Methodist Estabrook Cancer Center Methodist Jennie Edmundson Hospital
Gender
Male or Female
Age
60 years and older
Enrollment Status
Suspended
Phase
Phase II
Methodist Health System Trial Code
A041701