Clinical Trials Directory

Trials / Terminated

TerminatedNCT03516760

Dose-escalating Phase I Trial With GEM333 in Patients With Acute Myeloid Leukemia

A Multicenter, Open-label, Dose-escalating, Phase I Trial With GEM333, a CD33 Targeted Bispecific Antibody Engaging T-cells, in Relapsed or Refractory Acute Myeloid Leukemia

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
36 (actual)
Sponsor
AvenCell Europe GmbH · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This dose-escalating phase I trial assesses for the first time the safety, the side effects and the harmlessness, as well as the therapeutical benefit of the new study drug GEM333 in patients with acute myeloid leukemia (AML). This AML was relapsed after previous therapy or was refractory to the standard therapy.

Conditions

Interventions

TypeNameDescription
DRUGGEM333infusion of GEM333; administered intravenously and continuously over 10 days

Timeline

Start date
2018-04-11
Primary completion
2022-06-14
Completion
2022-06-14
First posted
2018-05-04
Last updated
2022-09-29

Locations

7 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT03516760. Inclusion in this directory is not an endorsement.

Dose-escalating Phase I Trial With GEM333 in Patients With Acute Myeloid Leukemia (NCT03516760) · Clinical Trials Directory