RecruitingPhase 1Phase 2NCT05186012

APG-1252 Monotherapy or in Combination With Other Therapeutic Agent in Subjects With Relapsed or Refractory Non-Hodgkin Lymphoma

A Phase Ib/II Study of APG-1252 as a Single Agent or in Combination With Other Therapeutic Agent in Patients With Relapsed and/or Refractory Non-Hodgkin Lymphoma(NHL)


Sponsor

Ascentage Pharma Group Inc.

Enrollment

51 participants

Start Date

Jun 14, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to assess the safety, pharmacokinetic, pharmacodynamic and efficacy of APG-1252 single agent and in combination with other therapeutic agent in patients with NHL.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing a drug called APG-1252, either alone or in combination with other cancer drugs, in patients with non-Hodgkin lymphoma (NHL) or peripheral T-cell lymphoma (PTCL) that has come back or stopped responding to treatment. **You may be eligible if...** - You have been diagnosed with relapsed or refractory non-Hodgkin lymphoma or peripheral T-cell lymphoma - You have received at least one prior treatment - You are in reasonably good health (ECOG score 0 or 1) - Your bone marrow, liver, kidney, and heart function are within acceptable ranges - You are willing to use effective contraception during the study **You may NOT be eligible if...** - You have received a stem cell transplant within the past 6 months - You have lymphoma that has spread to the brain - You have significant heart disease or a history of blood clots - You are currently pregnant or breastfeeding - You have uncontrolled infections including active hepatitis B, hepatitis C, or HIV - You have previously been treated with a BCL-xL inhibitor Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAPG-1252

APG-1252 administered via intravenous infusion for 30 minutes weekly (Day 1, 8, 15, 22).Every 28 days as a cycle.

DRUGChidamide

Chidamide 30mg orally BIW. Every 28 days as a cycle.


Locations(4)

Jiangsu Province Hospital

Nanyang, China

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Henan Provincial Oncology Hospital

Zhengzhou, Henanan, China

Shanghai Jiao Tong University school of medicine Ruijin Hospital

Shanghai, China

View Full Details on ClinicalTrials.gov

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NCT05186012


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