Natural Killer(NK) Cell Therapy Targeting CLL1 in Acute Myeloid Leukemia

NCT ID: NCT06027853

Last Updated: 2023-09-07

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-09-10
• Study Completion Date: 2026-08-31

Brief Summary

This is a phase 1, first-in-human (FIH), open-label, multicohort study to evaluate the safety, tolerability and preliminary efficacy of CLL1 target CAR iPSC NK cells in patients with relapsed/refractory AML

Detailed Description

Acute myelogenous leukemia (AML) is a potentially cur-able disease; 70% of newly diagnosed patients achievecomplete remission with first-line therapy, but prognosisworsens for relapsed disease in both pediatric and adultpatients. CLL-1 has attracted the researchers' attention due to its high expression in AML while being absent in normal hematopoietic stem cell. Accumulating evidence have demonstrated CLL-1 is an ideal target for AML.

Conditions

AML, Adult

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

CAR-NK cell therapy in Adult subjects with r/r AML

CAR-NK cell therapy in Adult subjects with r/r AML

Group Type: EXPERIMENTAL

CLL1 CAR-NK cell injection

Intervention Type: DRUG

Drug: CLL1 NK cell therapy Drug: Cyclophosphamid Lympho-conditioning Agent Drug: Fludarabine Lympho-conditioning Agent

Drug: VP-16 Lympho-conditioning Agent

Interventions

CLL1 CAR-NK cell injection

Drug: CLL1 NK cell therapy Drug: Cyclophosphamid Lympho-conditioning Agent Drug: Fludarabine Lympho-conditioning Agent

Drug: VP-16 Lympho-conditioning Agent

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. ≥18 years old.

2. Confirmed diagnosis of r/r AML

3. CLL1 expression is positive in AML blasts.

4. Eastern Cooperative Oncology Group (ECOG) performance status ≤1 and life expectancy greater than 12 weeks.

5. Adequate organ and marrow function, as defined below:

1. Blood creatinine (Cr) ≤ 2 x ULN or calculated creatinine clearance (Cockcroft- Gault formula) ≥ 50 mL/min;

2. Total bilirubin (TBIL) ≤ 2 x the ULN;

3. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 x ULN;

4. International normalized ratio (INR) and activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN

6. Females of childbearing potential must have a negative serum pregnancy test.

7. Donor specific antibody (DSA) is negative: MFI <= 2000.

8. Provision of signed and dated informed consent form (ICF).

Exclusion Criteria

1. Allergic to drug used in this study.

2. Subjects received any antitumor therapy as follows, prior to first NK infusion:

1. Systemic steroid therapy within 3 days (except physiological replacement therapy);

2. Systemic antitumor therapy within 2 weeks or at least 5 half-lives, whichever is less;

3. Radiotherapy within 4 weeks;

4. Donor lymphocyte infusion within 6 weeks;

5. Intrathecal treatment within 1 week;

6. CAR-T therapy, CAR-NK therapy, or any other genetically modified cell therapy product within 6 months;

3. History of allogeneic stem cell transplantation.

4. Received the vaccine within 4 weeks prior to the first infusion and/or expected to require vaccination from the study period to 12 weeks after the last infusion.

5. Active central nervous system Leukemia.

6. Acute Promyelocytic Leukemia (APL).

7. History of other malignant tumors, except for those who have achieved complete remission more than 5 years after radical treatment without any signs of recurrence.

8. Active autoimmune diseases.

9. History of central nervous system disease or meningeal involvement such as epilepsy, paralysis, aphasia, stroke, etc.

10. Serious cardiovascular and cerebrovascular diseases:

1. Severe heart rhythm or conduction abnormalities, corrected QT interval (QTc)≥480 ms;

2. Acute coronary syndrome, congestive heart failure, aortic dissection, stroke, or other grade 3 or higher cardiovascular and cerebrovascular events within 6 months prior to first infusion;

3. New York Heart Association (NYHA) class II or above congestive heart failure or left ventricular ejection fraction (LVEF) <50% in color Doppler echocardiography;

4. Hypertension that cannot be controlled by drug.

11. Active pulmonary infection; SpO2 ≤90%; Pulmonary embolism, chronic obstructive pulmonary disease, or interstitial lung disease.

12. Uncontrolled bacterial, fungal, or viral infection. Known HIV infection, active Hepatitis B (HBV) or Hepatitis C (HCV) infection.

13. History of substance abuse.

14. Toxicity induced by previous therapy not recovered to ≤ grade 2(NCI-CTCAE v5.0).

15. Large surgical treatment within 4 weeks prior to first infusion, not including diagnostic biopsy.

16. Pregnant/breastfeeding women.

17. Investigator-assessed presence of any medical or social issues that are likely to interfere with study conduct or may cause increased risk to subject.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hangzhou Qihangene Biotech Co.,Ltd.

UNKNOWN

Sponsor Role: collaborator

Zhejiang University

OTHER

Sponsor Role: lead

Responsible Party

He Huang

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

He Huang, MD

Role: PRINCIPAL_INVESTIGATOR

First Affiliated Hospital of Zhejiang University

Locations

Clinical research ethics committee of the first affiliated hospital, college of medicine, zhejiang University

Hangzhou, Zhejiang, China

Site Status: RECRUITING

Countries

China

Central Contacts

He Huang, MD

Role: CONTACT

hehuangyu@126.com

+8613605714822

Yongxian Hu, MD

Role: CONTACT

huyongxian2000@aliyun.com

+8615957162012

Facility Contacts

He Huang

Role: primary

hehuang@zju.edu.cn

0571-87233772

Other Identifiers

QH-CLL1-01

Identifier Type: -

Identifier Source: org_study_id