ClinicalTrials.gg
RecruitingNCT07424833Updated Oct 15, 2026

A Study of APG-3288 in Relapsed/Refractory Blood Cancers

A Phase 1 interventional study of APG-3288 in Relapsed/Refractory Hematological Malignancies, Relapsed/Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Leukemia (CLL/SLL and Relapsed/Refractory Diffuse Large B-cell Lymphoma (DLBCL; Including Richter Transformation), sponsored by Ascentage Pharma Group Inc.. Recruiting at 6 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-15.

Sponsored by Ascentage Pharma Group Inc. (part of Ascentage Pharma Group International) · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Started Mar 2026; still recruiting 8 months later.
Updated Oct 15, 2026Site recruiting status changedStart date movedGo to Updates ↓
Phase
Phase 1
Study type
Interventional
Enrollment
180
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This is a Phase I, multicenter, open-label, two-stage study of APG-3288 monotherapy, aiming to determine the Maximum Tolerated Dose (MTD) and Recommended Phase 2 Dose (RP2D) of APG-3288 administered orally once daily in patients with relapsed/refractory (R/R) hematologic malignancies.

Read the detailed description

Part 1 (Dose Escalation Phase): Patients will receive orally administered APG-3288 at specified doses once daily in 28-day cycles. This phase aims to determine the MTD or RP2D of APG-3288 for patients who have failed standard therapy and for whom no standard therapy offering clinical benefit is available.

Part 2 (Dose Expansion Phase): Following the completion of Part 1, Part 2 will be initiated to further evaluate dose safety. Doses will be determined based on a comprehensive assessment of the pharmacokinetic (PK), pharmacodynamic (PD), safety, and efficacy data of APG-3288 from Part 1. In Part 2, up to 60 patients per chosen indication will be enrolled and randomly assigned in equal proportions to 2 or 3 dose cohorts to evaluate dose safety.

02

Conditions studied

  • Relapsed/Refractory Hematological Malignancies
  • Relapsed/Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Leukemia (CLL/SLL
  • Relapsed/Refractory Diffuse Large B-cell Lymphoma (DLBCL; Including Richter Transformation)
  • Relapsed/Refractory Mantle Cell Lymphoma (MCL)
  • Relapsed/Refractory Waldenström Macroglobulinemia (WM)
  • Relapsed/Refractory Marginal Zone Lymphoma (MZL)
  • Relapsed/Refractory Follicular Lymphoma (FL)

Keywords

  • Relapsed/Refractory Hematological Malignancies
  • APG-3288
03

In context

Hematologic Neoplasms

1,444 studies on the registry are indexed under Hematologic Neoplasms; 420 are open to participants now.

This study's planned enrollment of 180 is above the median of 46 across 1,044 interventional studies indexed under Hematologic Neoplasms.

Browse Hematologic Neoplasms studies →

Lead sponsor

Ascentage Pharma Group Inc. is the lead sponsor of 53 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Key Inclusion Criteria:

  • (ECOG) status ≤ 1 in Part 1 (dose escalation), and ≤ 2 in Part 2 (dose expansion).
  • Part 1 (Dose Escalation): or cytologically confirmed diagnosis of R/R CLL/SLL, DLBCL (including Richter Transformation), MCL, WM, MZL, or FL.
  • Prior systemic therapy: at least 2 (including BTK inhibitor for approved indications) and who have failed or are not eligible for available therapies with established clinical benefit.
  • per response criteria specific to the malignant condition.
  • Adequate organ and bone marrow function.

Key Exclusion Criteria:

  • Concurrent anti-cancer therapy (chemotherapy, radiation therapy, surgery, immunotherapy, hormonal therapy, targeted therapy, biologic therapy, with the exception of hormones for hypothyroidism or estrogen replacement therapy, anti-estrogen analogs, agonists required to suppress serum testosterone levels).
  • Any therapy within 14 days prior to the first dose of study drug or within 5 half-lives of the respective investigational drug (whichever is shorter).
  • Persistent toxicities from prior radiotherapy, targeted therapy, immunotherapy, or chemotherapy agents that have not recovered to Grade \<2 (except for alopecia or vitiligo).
  • Symptomatic due to tumor involvement of the central nervous system (CNS). Patients with CNS tumors who have been treated, are asymptomatic, and who have discontinued (for the treatment of CNS tumors) for > 28 days may be enrolled.
  • Use of therapeutic-dose anticoagulants or antiplatelet agents. (Use of low-dose anticoagulants to maintain central venous catheter patency is permitted)
  • Biological growth factors within 7 days prior to the first dose of study drug.
  • Patients who, in the investigator's judgment, have not adequately recovered from prior surgery, or have undergone major surgery within 28 days prior to enrollment, or minor surgery within 14 days prior to enrollment.
  • Significant cardiac disease defined as:

    1. class III or IV cardiac disease, including pre-existing uncontrolled, clinically-significant arrhythmia, congestive heart failure, or cardiomyopathy.
    2. Unstable angina, myocardial infarction, or a coronary revascularization procedure within ≤ 3 months prior to initiation of study treatment.
    3. History of \< 50%.
    4. Poorly controlled hypertension, or history of poor compliance with antihypertensive drug regimens.
  • Clinically active and uncontrolled symptomatic infection; well-controlled (HIV), virus (HBV), or virus (HCV) infection may be considered for enrollment.
  • diseases, active inflammatory bowel disease, chronic infections, or any other disease or condition associated with chronic inflammation.
  • Concurrent use of -prolonging medications or history of torsades de pointes.
  • Concurrent other than the one being treated in this study with the exception of the following: cured malignancy without recurrence within 3 years prior to study entry; completely resected basal cell and squamous cell skin cancer; completely resected carcinoma in situ of any type.
  • Any severe and/or uncontrolled medical condition that, in the investigator's opinion, may compromise the individual's safety or the evaluation of study results.
  • Prior treatment with: BTK degrader treatment or stem cell transplant
Terms in these criteria, in plain language(16)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

Line of therapy

A line of therapy is one course of treatment, which may combine several drugs. First-line is the first course given; second-line follows when that stops working or is not tolerated.

“Two prior lines” means two courses that count separately under the study’s rules — not simply two drugs. Ask the study team if you are unsure how yours are counted.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Allogeneic and autologous transplant

Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
180 participants (estimated)

Study arms

  • Experimental
    Part 1 (Dose Escalation Phase)

    APG-3288 at multiple dose levels will be evaluated to determine the recommended phase 2 dose (RP2D) or maximum tolerated dose (MTD).

    Drug: APG-3288

  • Experimental
    Part 2 (Dose Expansion Phase)

    Indications and dose cohorts to be determined from Part 1

    Drug: APG-3288

Interventions

  • DrugAPG-3288

    Orally administered daily; 28 days per cycle.

06

What researchers measure

Primary outcomes

  1. Incidence of dose-limiting toxicities (DLTs) at each dose level

    A DLT is defined as any treatment-related adverse event (TRAE) meeting protocol-specified toxicity criteria occurring during the DLT evaluation period (Cycle 1). DLTs will be assessed in participants receiving escalating dose levels of APG-3288 to evaluate its safety and tolerability.

    Time frame: From first dose through the end of Cycle 1 (e.g., Day 1 to Day 28)

  2. Incidence of treatment emergent adverse events (TEAEs)

    The incidence of treatment emergent adverse events (TEAEs), including Grade 3-5 TEAEs, serious adverse events (SAEs), TEAEs leading to dose interruption, dose reduction, or treatment discontinuation, and deaths, will be assessed in participants receiving APG-3288 in Part 1 (dose escalation) and Part 2 (dose expansion) of the study.

    Time frame: From first dose of study treatment through 30 days after the last dose

  3. Maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of APG 3288

    The MTD and/or RP2D of APG-3288 will be determined during the dose escalation phase based on the incidence of DLTs, overall safety, tolerability, and available pharmacokinetic and pharmacodynamic data.

    Time frame: During the dose escalation phase (Part 1)

Secondary outcomes

  1. Peak plasma concentration (Cmax) of APG-3288

    The assessment of maximum observed plasma concentration (Cmax) following administration of APG-3288.

    Time frame: From first dose through 24 hours post-dose

  2. Area Under the Plasma Concentration-Time Curve (AUC) of APG-3288

    Area under the plasma concentration vs time curve (AUC0-t and AUC0-inf) of APG-3288 following administration APG-3288 at escalating dose levels.

    Time frame: From first dose through last measurable concentration, assessed up to 24 hours post-dose

  3. Pharmacodynamic (PD) profile of APG 3288

    The pharmacodynamic effects of APG 3288 will be evaluated by changes in Bruton's tyrosine kinase (BTK) levels from baseline over time during treatment.

    Time frame: From baseline of study treatment through 30 days after the last dose

  4. Objective response rate (ORR)

    ORR is defined as the proportion of patients who achieve partial response (PR) or better as assessed by the investigator at each efficacy assessment and upon disease progression or at end-of-treatment

    Time frame: From first dose until the first documented disease progression or end of treatment, assessed up to 24 months

  5. Duration of response (DoR)

    DoR is defined as duration in days from the date of initial documentation of a response (PR or better) to the date of first documented evidence of progressive disease for responders (PR or better) as assessed by the investigator or death due to any cause, whichever occurs first.

    Time frame: From the first documented response until disease progression or death, assessed up to 24 months

  6. Time to response (TTR)

    TTR is defined as the time interval from date of first dose of study drug to the date of initial documentation of a response (PR or better) as assessed by the investigator.

    Time frame: From first dose until the first documented response, assessed up to 24 months

  7. Progression free survival (PFS)

    PFS is defined as the time interval from date of first dose of study drug to the date of initial documentation of disease progression or death due to any cause, whichever occurs first, as assessed by the investigator.

    Time frame: From first dose until the first documented disease progression or death, whichever occurs first, assessed up to 24 months

  8. Overall survival (OS)

    OS is defined as the time interval from date of first dose of study drug to the date of death due to any cause.

    Time frame: From first dose until death from any cause, assessed up to 24 months

07

Study locations

5 of 6 sites recruiting
  • START Los Angele
    Los Angeles, California 90025, United States
    Recruiting
  • Mayo Clinic
    Jacksonville, Florida 32224, United States
    Recruiting
  • START Midwest
    Grand Rapids, Michigan 49546, United States
    Recruiting
  • START New Jersey
    East Brunswick, New Jersey 08816, United States
    Recruiting
  • The University of TX MD Anderson Cancer Center
    Houston, Texas 77030, United States
    Not yet recruiting
  • Henan Cancer Hospital
    Zhengzhou, Henan, China
    Recruiting
    • Keshu Zhou, M.D.,Ph.D. · Contactdr_zkshu23810@163.com · 13674902391
    • Keshu Zhou, M.D.,Ph.D. · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Sites
Mayo Clinic is now Recruiting
Oct 15, 2026
Start date
Aug 2026→Mar 10, 2026 (actual)
Oct 15, 2026
Show all 1 update
  1. Oct 15, 2026
    Mayo Clinic is now Recruiting
    Start date Aug 2026→Mar 10, 2026 (now actual)
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07424833
Responsible party
Sponsor
First posted
Feb 20, 2026
Start date
Mar 10, 2026
Primary completion
Dec 2029 (estimated)
Completion
Dec 2031 (estimated)
Last update
Oct 15, 2026

Study contacts

Yifan Zhai, M.D., Ph.D.
Contact
Yzhai@ascentage.com
18998334688
Qiwei Chen, M.D.
Contact
Qiwei.Chen@ascentage.com
Keshu Zhou, M.D.,Ph.D.
principal investigator · Henan Cancer Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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