Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT05147467

Study of APG-2575 in Patients With Relapsed/Refractory CLL/SLL

Led by Ascentage Pharma Group Inc. · Updated on 2026-03-27

75

Participants Needed

11

Research Sites

309 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to assess the efficacy and safety of APG-2575 single agent in patients with relapsed/refractory CLL/SLL.

CONDITIONS

Official Title

Study of APG-2575 in Patients With Relapsed/Refractory CLL/SLL

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Pathologically confirmed Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma with measurable lesions or splenomegaly
  • Expected survival of at least 12 weeks
  • Refractory, recurrent, or intolerant to BTK inhibitors and immunochemotherapy, or first-line BTK inhibitor treatment failure and not suitable for immunochemotherapy
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 2
  • Ability to understand and willingness to sign informed consent
  • Willingness and ability to comply with study procedures and follow-up
Not Eligible

You will not qualify if you...

  • History of allogeneic hematopoietic stem cell transplantation, adoptive cell immunotherapy, or autologous hematopoietic stem cell transplantation within 24 months
  • Incomplete recovery from prior surgery; major surgery within 28 days or minor surgery within 14 days before study entry
  • Prior treatment with Bcl-2 inhibitors
  • Invasive non-Hodgkin lymphoma transformation or central nervous system involvement
  • Pregnancy, lactation, or pregnancy expected during the study or within 3 months after last treatment
  • History of active malignant tumors other than CLL/SLL within 2 years, except fully treated cervical carcinoma in situ or fully resected basal cell or localized squamous cell skin carcinoma
  • Any other condition that investigators consider makes participation unsuitable

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 11 locations

1

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, China, 510060

Actively Recruiting

2

Zhujiang Hospital of Southern Medical University

Guangzhou, Guangdong, China, 510280

Not Yet Recruiting

3

Nanfang Hospital of Southern Medical University

Guangzhou, Guangdong, China, 510515

Actively Recruiting

4

Hainan General Hospital

Haikou, Hainan, China, 570311

Not Yet Recruiting

5

Henan Cancer Hospital

Zhengzhou, Henan, China, 450003

Actively Recruiting

6

Union Hospital medical college Huazhong University of Science and Technology

Wuhan, Hubei, China, 430022

Actively Recruiting

7

The First Affilated Hospital of Soochow University

Suzhou, Jiangsu, China, 215006

Not Yet Recruiting

8

People's hospital of Jiangsu Province

Suzhou, Jiangsu, China

Not Yet Recruiting

9

The First Affilated Hospital of Nanchang University

Nanchang, Jiangxi, China, 330006

Not Yet Recruiting

10

Institute of blood transfusion of Chinese Academy of Medical Sciences

Tianjin, Tianjin Municipality, China, 215127

Not Yet Recruiting

11

The First Affiliated Hospital of Zhejiang University School of Medicine

Hanzhou, Zhejiang, China, 310003

Not Yet Recruiting

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Research Team

Z

Zi Chen, Doctor

CONTACT

M

Min Yu, Doctor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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