Clin2
NCT03737955Possibly a fitRecruiting

Gemtuzumab for measurable residual leukemia after initial treatment

Acute Myeloid Leukemia

Treatments studied

Part of Blood & lymphatic, Cancer clinical trials.

This trial studies whether fractionated gemtuzumab can eliminate tiny, hard-to-see leukemia cells left after standard chemotherapy. It targets adults with acute myeloid leukemia (AML) who have measurable residual disease (MRD) rather than active leukemia in the blood.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
36 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have been diagnosed with AML (but not acute promyelocytic leukemia, or APL; and not biphenotypic AML)
  • Your leukemia must be MRD-positive only (less than 5% blast cells in bone marrow) and meet criteria for a response like complete remission or CR with incomplete blood recovery
  • Your MRD must be measurable using specific tests (flow cytometry and/or PCR/molecular tests and/or chromosome/cytogenetic tests)
  • You must have had at least one cycle of standard induction chemotherapy before joining (you can join at different times after that as an adult)
  • Your leukemia cells must have CD33 on them, and you must be age 18+ with good enough general functioning
  • You must be well enough for treatment based on organ lab tests (kidney, liver) and you must be able to sign consent; pregnancy test must be negative if applicable

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT04168502Recruiting· Phase 3
Gemtuzumab added to chemotherapy for certain adult AML

This Phase 3 trial tests whether adding gemtuzumab to standard chemotherapy helps people with newly diagnosed, favorable-intermediate AML reduce “MRD” (very small remaining leukemia cells). If MRD levels drop more, it may lower the chance of relapse.

Alessandria
NCT04385290Recruiting· Phase 1/Phase 2
Testing midostaurin plus gemtuzumab for newly diagnosed AML

This trial studies whether combining two medicines—midostaurin and gemtuzumab (with standard chemotherapy)—can improve outcomes for newly diagnosed acute myeloid leukemia (AML). It is testing a first-line treatment plan tailored to specific genetic changes in the leukemia.

München, Bavaria
NCT06448013Recruiting· Phase 1
Ziftomenib with chemo for pediatric AML

This trial tests a new drug, ziftomenib, combined with two standard chemotherapies (venetoclax and gemtuzumab) for children and young adults with acute myeloid leukemia (AML) that has come back or not responded to treatment. It looks for specific genetic changes in the leukemia cells.

Houston, Texas
NCT05554419Not yet recruiting· Phase 2
Study for persistent low-level AML after initial remission

This Phase 2 trial tests a combination treatment to try to get rid of remaining cancer cells in young adults whose acute myeloid leukemia (AML) is in remission but still detectable at low levels. It may help patients eliminate “minimal residual disease” (small traces of leukemia cells) and reduce relapse risk.

NCT05558124Recruiting· Phase 1
Tested CPX-351 with gemtuzumab for newly diagnosed AML

This Phase 1 trial tests a new combination of CPX-351 plus gemtuzumab ozogamicin for people newly diagnosed with acute myeloid leukemia (AML). It aims to find a safe dose and see how well the treatment works, especially when the leukemia cells carry a target called CD33.

Tampa, Florida
NCT06769490Recruiting· Phase 1
Ziftomenib and Quizartinib combination for AML

This trial tests two targeted drugs, ziftomenib and quizartinib, together for people with a certain type of acute myeloid leukemia (AML) that has come back or not responded to treatment. The goal is to find the best dose and see if the combination helps.

Houston, Texas

Hear when a new Acute Myeloid Leukemia trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.