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NCT07188610RecruitingPhase 2

PA3-17 Injection in Adult Patients With CD7-positive Relapsed/Refractory T-lymphoblastic Leukemia/Lymphoma

PA3-17 Injection for the Treatment of Subjects With Relapsed/Refractory T-Lymphoblastic Leukemia/Lymphoma: A Single-Arm, Open-Label Phase II Clinical Trial

Source: ClinicalTrials.gov · Last updated 6 Jul 2026

Brief summary (registry, in English)

\*\*Translation:\*\* This clinical trial is designed as a single-arm, open-label, multicenter study. After signing the informed consent form, eligible subjects will undergo a single nucleated cell collection for the preparation of CAR-T cells. Following lymphodepletion pretreatment, a single infusion of PA3-17 injection will be administered. Blood samples will be collected from the subjects before and after the infusion for pharmacokinetic, pharmacodynamic, immunogenicity, and safety evaluations. In addition to the baseline period, the treatment phase will involve efficacy assessments at 4 weeks, 2 months, 3 months, and every 3 months thereafter, up to 24 months post-cell infusion. Tumor assessments will continue until disease progression (PD), initiation of new antitumor treatment, death, unacceptable toxicity, investigator decision, or subject's voluntary withdrawal, whichever occurs first.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
100 (estimated)
First submitted
16 Sept 2025
Start date
25 Sept 2025
Primary completion date
1 Oct 2026
Lead sponsor
PersonGen BioTherapeutics (Suzhou) Co., Ltd.
NCT number
NCT07188610

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 100
  • From 25 Sept 2025 to the primary completion date, 1 Oct 2026
  • 16 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subjects who have received CAR-T therapy or other gene-modified cell therapy before screening;
  • Participation in other clinical studies within 1 month before screening (end date of the last application of unapproved innovative drugs);

Other illness

  • Known to have active or uncontrolled autoimmune diseases;
  • History of malignant tumors other than T-ALL/LBL within the past 5 years, except for adequately treated cervical intraepithelial neoplasia, basal cell or squamous cell skin cancer, locally treated prostate cancer, and ductal carcinoma in situ of the breast after radical surgery;
  • Positive test results for hepatitis B, hepatitis C, syphilis, etc.;
  • Severe heart disease;
  • Unstable systemic diseases as judged by the investigator;
  • Presence of active infection or uncontrollable infection requiring systemic treatment;

Other

  • Presence of GvHD;
  • Pregnant or breastfeeding women, and female subjects planning to conceive within 2 years after cell infusion, or male subjects whose partners plan to conceive within 2 years after cell infusion;
  • Evidence of central nervous system involvement at the time of subject screening;
  • Situations judged by the investigator as not suitable for cell preparation;
  • Other circumstances deemed unsuitable for enrollment by the investigator.

Who the study is looking for

  • Age and Gender: ≥18 years old (inclusive), regardless of gender.
  • Survival Expectancy: ≥3 months.
  • Performance Status: ECOG score 0-1.
  • Diagnosis: Confirmed acute T-cell lymphoblastic leukemia/lymphoma (T-ALL/LBL) according to the WHO fifth edition of the "Classification of Hematopoietic and Lymphoid Tumors," including early T-cell precursor (ETP).
  • Recurrent or Refractory Disease: Subjects with recurrent/refractory T-ALL/LBL (including ETP-ALL/LBL).
  • Screening: Abnormal cells CD7 expression positive.
  • Lesion Assessment: If the subject has only extramedullary lesions, they must have evaluable lesions.
  • Meet the requirements of liver, kidney, heart, and lung functions.
  • No Severe Mental Disorders.
  • Informed Consent: Ability to understand the trial and signed informed consent form.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University People's Hospital
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BeijingChinaRecruiting
Peking University Third Hospital
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BeijingChinaRecruiting
West China Hospital, Sichuan University (WCHSU)
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ChengduChinaRecruiting
Facility Name: Guangdong Provincial People's Hospital
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GuangzhouChinaNot yet recruiting
Sun Yat-sen University Cancer Center (SYSUCC)
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GuangzhouChinaRecruiting
The First Affiliated Hospital Zhejiang University School of Medicine
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HangzhouChinaNot yet recruiting
The First Hospital of Harbin
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HarbinChinaNot yet recruiting
The First Affiliated Hospital of University of Science and Technology of China (Anhui Provincial Hospital)
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HefeiChinaRecruiting
Jiangsu Province Hospital
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NanjingChinaRecruiting
Tongji Hospital Tongji University
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ShanghaiChinaRecruiting
The First Affiliated Hospital of Soochow University
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SuzhouChinaRecruiting
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences
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TianjinChinaRecruiting
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
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WuhanChinaRecruiting
The affiliated hospital of xuzhou medical university
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XuzhouChinaRecruiting
Henan Cancer Hospital
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ZhengzhouChinaRecruiting
The First Affiliated Hospital of Zhengzhou University
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ZhengzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.