Acute Myeloid Leukemia Clinical Trial

Study of AMG 330 in Combination With Pembrolizumab in Adult With Relapsed or Refractory Acute Myeloid Leukemia

Summary

The primary objective of this study is to evaluate the safety and tolerability of AMG 330, administered in combination with pembrolizumab, in participants with relapsed or refractory acute myeloid leukemia (R/R AML).

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Full Description

This study will assess the safety and tolerability of AMG 330 in combination with pembrolizumab and whether pembrolizumab will enhance the anti-AML activity of AMG 330. Both cohort 1 and 2 will include AMG 330 and pembrolizumab with the difference being the initiation date for pembrolizumab treatment.

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Eligibility Criteria

Key Inclusion criteria

AML as defined by the WHO Classification persisting or recurring following one or more treatment courses. Except APL
Eastern Cooperative Oncology Group (ECOG) ≤1

Key Exclusion criteria

Active extramedullary AML in the central nervous system.
Known hypersensitivity to immunoglobulins.
Non-manageable graft versus host disease.

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 1

Estimated Enrollment:

1

Study ID:

NCT04478695

Recruitment Status:

Terminated

Sponsor:

Amgen

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There are 2 Locations for this study

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City of Hope National Medical Center
Duarte California, 91010, United States
University of Texas MD Anderson Cancer Center
Houston Texas, 77030, United States

How clear is this clinincal trial information?

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 1

Estimated Enrollment:

1

Study ID:

NCT04478695

Recruitment Status:

Terminated

Sponsor:


Amgen

How clear is this clinincal trial information?

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