Study of AZD9829 in CD123+ Hematological Malignancies
Launched by ASTRAZENECA · Dec 19, 2023
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new treatment called AZD9829 for patients with certain blood cancers that have a specific marker called CD123. This study is in the early phases and aims to find the best dose of AZD9829, which may be given alone or with other treatments. It is currently open to adults aged 18 and older who have specific types of blood cancers, such as relapsed or refractory acute myeloid leukemia (AML) or high-risk myelodysplastic syndromes (HR-MDS). To be eligible, participants should have already tried at least one other treatment that didn’t work and should not have any other treatment options available.
If you join this trial, you will receive AZD9829 through an intravenous (IV) line, and the study team will closely monitor your health and the treatment's effects. It’s important to know that there are some criteria that could exclude you from participating, such as having an active central nervous system leukemia, previous treatments targeting CD123, or certain other serious health issues. This trial is actively recruiting participants, so if you meet the eligibility requirements and are interested, it could be a potential option for you or your loved one.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • ≥18 years of age;
- • CD123+ hematologic malignancy based on flow cytometry or immunohistochemistry by local laboratory;
- • R/R AML (except APL);
- • R/R HR-MDS with ≥5% bone marrow blast at time of inclusion;
- • Had at least 1 prior line of therapy at currents histology, and have no available treatment options;
- • ECOG performance status of ≤ 2.
- • The above is a summary, other inclusion criteria details may apply.
- Exclusion Criteria:
- • Active CNS leukemia;
- • Previous treatment with any CD123 targeting therapy;
- • Prior allogeneic HSCT, within 90 or cell therapy within 60 of start of therapy;
- • Active GVHD that requires immunosuppressive treatment within 4 weeks prior to start of AZD9829;
- • History of other malignancy(with certain exceptions);
- • Active and uncontrolled infections;
- • Unresolved AEs ≥2 Grade, from prior therapies.
- • The above is a summary, other exclusion criteria details may apply.
About Astrazeneca
AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Barcelona, , Spain
New York, New York, United States
Houston, Texas, United States
Salamanca, , Spain
Tainan, , Taiwan
Columbus, Ohio, United States
Heidelberg, , Australia
Saint Louis, Missouri, United States
Milwaukee, Wisconsin, United States
New York, New York, United States
Duarte, California, United States
Frankfurt, , Germany
Bologna, , Italy
Taipei, , Taiwan
Seoul, , Korea, Republic Of
Kashiwa, , Japan
Zhengzhou, , China
Osaka Shi, , Japan
Guangzhou, , China
Tianjian, , China
Chapel Hill, North Carolina, United States
Yoshida Gun, , Japan
Tianjin, , China
Melbourne, , Australia
Chapel Hill, North Carolina, United States
Manchester, , United Kingdom
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported