72 Participants Needed

AZD2962 for Cancer

Recruiting at 16 trial locations
AC
Overseen ByAstraZeneca Clinical Study Information Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new drug, AZD2962, designed to treat certain blood cancers. Researchers aim to determine if AZD2962 is safe and effective both alone and in combination with other treatments. The study targets individuals with myelodysplastic syndromes (MDS) or dysplastic chronic myelomonocytic leukemia (CMML) that have recurred or resisted other treatments. Participants should exhibit noticeable symptoms requiring treatment. As a Phase 1/Phase 2 trial, this research seeks to understand how the treatment works in people and measure its effectiveness in an initial, smaller group, offering participants a chance to be among the first to benefit from this new therapy.

Will I have to stop taking my current medications?

The trial requires that you stop taking certain medications before starting, such as antineoplastic therapies, strong or moderate CYP3A inhibitors, and drugs that prolong QT interval, among others. Please consult with the trial team to see if your current medications are affected.

Is there any evidence suggesting that AZD2962 is likely to be safe for humans?

Studies have shown that AZD2962, the treatment being tested, is in the early stages of clinical trials. The main goal is to assess its safety and tolerability. As the study is just beginning, limited safety information is available. However, similar studies have not reported serious safety issues, suggesting that AZD2962 might be safe. More research is needed to confirm this. Participants in the trial will be closely monitored by the medical team to ensure safety.12345

Why do researchers think this study treatment might be promising?

Unlike the standard treatments for Myelodysplastic Syndromes (MDS) and dysplastic Chronic Myelomonocytic Leukemia (CMML), which often involve chemotherapy or supportive care, AZD2962 offers a novel approach by acting as a monotherapy with a unique mechanism. Researchers are excited about AZD2962 because it targets specific pathways involved in the disease progression, potentially offering a more targeted and less toxic alternative. This innovative drug also employs a dose escalation pattern, which could optimize its effectiveness while minimizing side effects, making it a promising option for patients who have limited choices with current therapies.

What evidence suggests that AZD2962 might be an effective treatment for cancer?

Research has shown that AZD2962 blocks a protein linked to inflammation and cancer growth. Early studies suggest it might help treat blood cancers like myelodysplastic syndromes (MDS) and dysplastic chronic myelomonocytic leukemia (CMML). In this trial, participants will receive AZD2962 as monotherapy in a dose escalation pattern. Although detailed information from human studies remains limited, AZD2962's mechanism gives scientists hope that it could stop cancer cells from surviving. While still in early stages, the potential of this treatment looks promising based on its targeted approach.14678

Are You a Good Fit for This Trial?

This trial is for individuals with blood cancers who can safely receive treatment. Specific details on eligibility are not provided, but typically participants must meet certain health standards and may need to have a particular type or stage of cancer.

Inclusion Criteria

All women of childbearing potential must have a negative serum pregnancy test result at Screening.
I can perform daily activities with minimal assistance.
My condition causes symptoms that need treatment and can be measured to see if the treatment is working.
See 3 more

Exclusion Criteria

I have had cancer before, but it wasn't related to blood.
Concurrent enrolment in another clinical study (with some exceptions).
Known hypersensitivity to study intervention or its excipients.
See 13 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

3 weeks

Treatment

Participants receive AZD2962 monotherapy in 28-day cycles until disease progression, unacceptable toxicity, or withdrawal

Approximately 3 years

Safety Follow-up

Participants are monitored for safety 30 days after the last dose

4 weeks

Follow-up

Participants are monitored for long-term safety and efficacy outcomes

Approximately 3 years

What Are the Treatments Tested in This Trial?

Interventions

  • AZD2962
Trial Overview The study tests AZD2962 alone and combined with other treatments in people with blood cancers. It looks at how safe it is, how the body processes it, its effects on the body (pharmacodynamics), and early signs of effectiveness.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Module 1- AZD2962 (Monotherapy)Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

AstraZeneca

Lead Sponsor

Trials
4,491
Recruited
290,540,000+

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

Parexel

Industry Sponsor

Trials
322
Recruited
137,000+
Peyton Howell profile image

Peyton Howell

Parexel

Chief Executive Officer

Master of Healthcare Administration from The Ohio State University, Bachelor of Arts in Health Communications from the University of Illinois

Dr. Austin Smith profile image

Dr. Austin Smith

Parexel

Chief Medical Officer since 2023

MD from the Royal College of Surgeons in Ireland

Citations

NCT07064122 | A Study of AZD2962, an IRAK4 Inhibitor ...This is a modular study. In Module 1, the study will begin with a dose escalation of AZD2962 monotherapy in participants with myelodysplastic syndromes ...
Real Life Data on Efficacy and Safety of Azacitidine ...Complete remission (CR) was achieved in 14% of MDS, 7% of AML and 10% of CMML patients. Overall response rate was following: 27% for MDS, 20% ...
Real Life Data on Efficacy and Safety of Azacitidine ...Complete remission (CR) was achieved in 14% of MDS, 7% of AML and 10% of CMML patients. Overall response rate was following: 27% for MDS, 20% ...
4.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/30613922/
Real Life Data on Efficacy and Safety of Azacitidine ...Complete remission (CR) was achieved in 14% of MDS, 7% of AML and 10% of CMML patients. Overall response rate was following: 27% for MDS, 20% ...
(PDF) Real Life Data on Efficacy and Safety of Azacitidine ...Complete remission (CR) was achieved in 14% of MDS, 7% of AML and 10% of CMML patients. Overall response rate was following: 27% for MDS, 20% for AML and 20% ...
Study of AZD2962 tablets alone and with other medications ...The main purpose of this research is to understand how safe the medication is and how well patients can tolerate it. The study will evaluate AZD2962 both when ...
A Study of AZD2962, an IRAK4 Inhibitor (IRAK4 [a Body ...The purpose of the study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary efficacy of AZD2962, ...
9M and Q3 2025 results clinical trials appendixBreast cancer, ovarian cancer, endometrial cancer, squamous NSCLC ... • Safety endpoints: safety and tolerability. • FPCD: Q2 2025.
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