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.

NCT03537482

APG-2575 Study of Safety, Tolerability ,PK/PD in Patients With Hematologic Malignancies

UNKNOWN
EARLY_PHASE1Ages 18+InterventionalTreatment
Ascentage Pharma Group Inc.
~90 participants
Updated 2024-08-19 on ClinicalTrials.gov
What's tested:APG-2575

At a glance

Recruiting sites
4 of 5 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Maximum Tolerated Dose (MTD)
Measured over 28 days
Hematologic Malignancies

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.

  • Yifan Zhai, MD, PhD · STUDY_CHAIR · Ascentage Pharma Group Inc.

Opens a ready-to-send draft in your own email app — review before sending.

  • 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