AZD3632 for Acute Myeloid Leukemia
(MOMENTUM Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests AZD3632, a new oral treatment, to determine its safety and effectiveness for individuals with advanced blood cancers such as acute myeloid leukemia. It explores different doses of AZD3632 alone and in combination with another drug, posaconazole. Individuals with relapsed or hard-to-treat leukemia or myelodysplastic syndrome (a blood disorder) who have specific genetic changes might be suitable candidates. As a Phase 1 trial, this research aims to understand how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment.
Do I have to stop taking my current medications for the trial?
The trial information does not specify if you need to stop taking your current medications. However, it mentions that participants should not have received certain anticancer agents or radiation therapy recently. It's best to discuss your specific medications with the trial team.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that AZD3632 is being tested for safety and tolerability in people with advanced blood cancers. These studies examine how the body processes the drug and its effects. Although detailed safety information is not yet available, the drug remains in the early stages of testing, requiring further research to understand its tolerance.
Similarly, studies are testing the combination of AZD3632 and posaconazole for safety and tolerability. These trials aim to determine the safety of this combination for participants. Like AZD3632 alone, these studies are in the early stages, so researchers are still learning about possible side effects.
With both treatments in early trials, information on side effects is limited. Participants in these studies help scientists learn about the risks and benefits of the treatments, a crucial step in developing new therapies.12345Why are researchers excited about this trial's treatments?
Researchers are excited about AZD3632 for treating acute myeloid leukemia (AML) because it represents a novel approach to tackling this aggressive cancer. Unlike traditional chemotherapy drugs, which often target rapidly dividing cells broadly, AZD3632 is designed to specifically interfere with the cancer cell's ability to survive and proliferate without harming normal cells as much. Additionally, some trial arms explore combining AZD3632 with posaconazole, which might enhance its effectiveness by adding an antifungal agent that could further protect patients with weakened immune systems. This combination approach adds a layer of innovation and potential increased safety and efficacy compared to existing treatment options.
What evidence suggests that this trial's treatments could be effective for acute myeloid leukemia?
Research shows that AZD3632 is being developed to target specific genetic changes found in some blood cancers, such as acute myeloid leukemia (AML). It disrupts the processes that help cancer cells grow. In this trial, participants will receive varying doses of AZD3632 to evaluate its effectiveness. Additionally, some participants will receive AZD3632 combined with posaconazole, which reduces the risk of infections—an important consideration for AML patients. Although data on AZD3632's effectiveness is still being gathered, its targeted approach offers hope for better outcomes in treating advanced blood cancers.14678
Are You a Good Fit for This Trial?
This trial is for adults with advanced blood cancers like Myelodysplastic Syndromes or various types of Leukemia. Participants must have specific genetic markers (KMT2Ar, NPM1m, or others linked to HOX overexpression). The full eligibility criteria are not provided here.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive AZD3632 monotherapy or in combination with posaconazole, with dose escalation in Module 1 and combination treatment in Module 2
Follow-up
Participants are monitored for safety and effectiveness after treatment, including assessment of treatment-emergent adverse events and pharmacokinetics
What Are the Treatments Tested in This Trial?
Interventions
- AZD3632
Find a Clinic Near You
Who Is Running the Clinical Trial?
AstraZeneca
Lead Sponsor
Sir Pascal Soriot
AstraZeneca
Chief Executive Officer since 2012
Veterinary Medicine from École nationale vétérinaire d'Alfort, MBA from HEC Paris
Dr. Cristian Massacesi
AstraZeneca
Chief Medical Officer since 2021
MD from Marche Polytechnic University, Oncology training at Royal Marsden Hospital, Kaplan Comprehensive Cancer Center, and European Institute of Oncology
Pascal Soriot
AstraZeneca
Chief Executive Officer since 2012
Veterinary Medicine from École nationale vétérinaire d'Alfort, MBA from HEC Paris
Cristian Massacesi
AstraZeneca
Chief Medical Officer since 2021
MD from Marche Polytechnic University, Medical Oncology training at Royal Marsden Hospital, Kaplan Comprehensive Cancer Center, and European Institute of Oncology