Study to Evaluate PK and Safety With Uproleselan Combined With Chemotherapy to Treat Chinese R/R AML Patients

NCT ID: NCT04839341

Last Updated: 2025-06-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-02-24
• Study Completion Date: 2024-06-28

Brief Summary

This study will evaluate the safety and tolerability of uproleselan(GMI-1271), a specific E-selectin antagonist, and characterize the pharmacokinetic (PK) profile of uproleselan, in combination with chemotherapy to treat Chinese relapsed/refractory AML patients.

Detailed Description

This study is a multicenter open-labelled study conducted in subjects with relapsed or refractory AML in China. The study includes the following phases: screening phase, induction phase, consolidation phase baseline, consolidation phase and follow-up period.

Screening phase:

This study will enroll 12 subjects, who are 18 to 60 years (inclusive) at the time of signing the Informed Consent Form (ICF), and with the diagnosis as relapsed or refractory AML. Screening is conducted 21 days to 2 days before administration, and signed ICF by the subject must be obtained before screening.

Baseline period:

The baseline period is 1 day before study drug administration.

Induction treatment:

During the induction phase, subjects will receive 8 consecutive days of uproleselan treatment and 5 consecutive days of MEC (mitoxantrone, etoposide, and cytarabine combined regimen) chemotherapy.

Consolidation baseline:

The baseline of the consolidation phase is 1 day before the treatment administration of the consolidation phase.

Consolidation treatment:

Subjects who met the criteria for consolidation treatment started the consolidation period at the 29th day of the previous treatment cycle at the earliest and the 65th day at the latest.

Follow-up period:

Each subject should complete the following follow-up stage: (1) Response evaluation to determine remission to the induction treatment (induction period); (2) EOT assessment after completing the last consolidation treatment cycle; (3) Death. Survival and long-term follow-up, including initiation of new anti-leukemia treatment (within 6 months after the last uproleselan/placebo administration), recurrence, HSCT and survival events, monthly (±14 days) for 2 years after the end of treatment, and afterwards quarterly (±14 days). The longest survival follow-up time is 3 years (calculated from the start of treatment).

Conditions

Relapsed/Refractory AML

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

A Phase I, open-labeled multicenter study

Uproleselan in combination with mitoxantrone, etoposide and cytarabine (MEC)

Group Type: EXPERIMENTAL

Uproleselan

Intervention Type: DRUG

A rationally designed E-selectin antagonist used to inhibit binding of cells to E-selectin

Interventions

Uproleselan

A rationally designed E-selectin antagonist used to inhibit binding of cells to E-selectin

Intervention Type: DRUG

Other Intervention Names

GMI-1271

Eligibility Criteria

Inclusion Criteria

1. ≥18 years and ≤60 years in age

2. AML (including secondary AML) diagnosed as per WHO standards (2008).

3. For refractory AML, only cytarabine/daunorubicin(or Idarubicin) as can be applied repeatedly(maximal twice) as induction, no other chemotherapy are allowed to be applied Venatoclax /hypomethylation drug [HMA] can be used before and after chemotherapy.

1. For relapse AML, it must be the first or second relapse, and remain untreated.

2. Certain regimens (Venatoclax/HMA, Venetoclax/LDAC, HMA single agent) and FLT3 inhibitors, tyrosine kinase inhibitors, IDH1/IDH2 inhibitors or similar targeted inhibitors used alone are not considered cytotoxic chemotherapy are allowed.

4. ECOG performance status score is 0 to 2.

5. Stable hemodynamics and good organ function.

Exclusion Criteria

1. Patients with acute promyelocytic leukemia, acute leukemia of ambiguous lineage (biphenotypic leukemia), chronic myeloid leukemia with myeloid blast crisis, or secondary refractory AML.

2. Active signs or symptoms of CNS involvement by malignancy.

3. Stem cell transplantation ≤4 months prior to dosing.

4. Any immunotherapy or radiotherapy therapy within 28 days of dosing; any other experimental therapy or chemotherapy within 14 days of dosing.

5. Prior use of G-CSF, CM-CSF or plerixafor within 7 days of dosing.

6. Inadequate organ function.

7. Abnormal liver function.

8. Known active infection with hepatitis A, B, or C, or human immunodeficiency virus.

9. Moderate kidney dysfunction (glomerular filtration rate <45 mL/min).

10. Uncontrolled acute life-threatening bacterial, viral, or fungal infection.

11. Clinically significant cardiovascular disease.

12. Major surgery within 4 weeks of dosing.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Apollomics Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jianxiang Wang, PhD

Role: PRINCIPAL_INVESTIGATOR

Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences

Locations

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

Tianjin, Tianjin Municipality, China

The First Affiliated Hospital of Zhejiang University

Hangzhou, , China

Countries

China

Other Identifiers

APL-106-01

Identifier Type: -

Identifier Source: org_study_id