APG-2575 for Hematologic Malignancies
This study is testing a new oral medication called APG-2575 for people with certain blood cancers (hematologic malignancies), including multiple myeloma, chronic lymphocytic leukemia, and non-Hodgkin's lymphoma. The main goal is to find the highest dose of APG-2575 that can be given safely without causing too many side effects. This is a Phase 1 study, meaning it's one of the first times this drug is being tested in people. You may be eligible if you are at least 18 years old and have one of the specified blood cancers. The study is currently unclear on its recruitment status and plans to enroll about 90 participants.
- Study design
- This is an open-label, single-arm Phase 1 study, meaning all participants will receive APG-2575 and both you and the study team will know which treatment you are getting. The study aims to enroll about 90 participants.
- What's involved
- APG-2575 will be taken as an oral tablet once daily for four consecutive weeks per cycle. The dose may be increased in subsequent cycles.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary endpoint, Maximum Tolerated Dose (MTD), is measured at 28 days.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
APG-2575 Study of Safety, Tolerability ,PK/PD in Patients With Hematologic Malignancies
At a glance
Conditions
NCT03537482
Where you'd take part
This study runs at 5 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Epworth Healthcare
Richmond, Victoria, Australiastudy coordinator listed
Recruiting
Mayo Clinic
Jacksonville, Floridastudy coordinator listed
Recruiting
MDACC
Houston, Texasstudy coordinator listed
Recruiting
St. Vincent Hospital
Fitzroy, Victoria, Australiastudy coordinator listed
Recruiting
Duke Unviersity
Durham, North Carolinano site contact published
Completed
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Yifan Zhai, MD, PhD · STUDY_CHAIR · Ascentage Pharma Group Inc.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Maximum Tolerated Dose (MTD)28 days
Patients with APG-2575 treatment related adverse events (AE), serious adverse events (SAE) will be assessed according NCI CTCAE Version 4.0