AZD2962 for Cancer
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
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive AZD2962 monotherapy in 28-day cycles until disease progression, unacceptable toxicity, or withdrawal
Safety Follow-up
Participants are monitored for safety 30 days after the last dose
Follow-up
Participants are monitored for long-term safety and efficacy outcomes
What Are the Treatments Tested in This Trial?
Interventions
- AZD2962
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
Parexel
Industry Sponsor
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
Parexel
Chief Medical Officer since 2023
MD from the Royal College of Surgeons in Ireland