UPCC 03418: A Phase 1 First in Human Open Label Dose Escalation Study of AMV564 a CD33 x CD3 Tandem Diabody in Patients with Relapsed or Refractory Acute Myeloid Leukemia

Enrolling By Invitation
99 years or below
All
Phase 1
10 participants needed
1 Location

Brief description of study

Amphivena Therapeutics, Inc. (Amphivena) is studying an investigational drug called AMV564, which may help to treat acute myeloid leukemia (AML). The purpose of this clinical research study is to find the highest tolerable dose that can be given to patients with AML, and to recommend a dose to be used in future studies. Another purpose of the study is to learn more about the safety of this drug and how the body processes the study drug.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Leukemia
  • Age: 99 years or below
  • Gender: All
Updated on 19 Feb 2024. Study ID: 829245
If you need help finding a study or have any questions, please contact us at psom-ocr@pobox.upenn.edu

 

Interested in the study?

Message For Enrolling By Invitation Trial

study is selecting its participants from a population, or group of people, decided on by the researchers in advance.

Contact a study center.