A Clinical Study to Observe the Safety and Efficacy of ScTIL210 in the Treatment of Malignant Solid Tumors

NCT04571892 | Unknown Phase 1

• 1 other identifier: ScTIL210-003-2020
• Study Type: interventional
• Target: 58
• Locations: 1 country
• Sites: 2

Brief Summary

An open-label, single-arm, single-dose escalation and multiple-dose expansion clinical study of cell therapy to observe and to evaluate the tolerance, the pharmacokinetic characteristics, the safety, and the efficacy of ScTIL210 in the treatment of malignant

Conditions

Malignant Solid Tumor

Outcome Measures

Primary Outcomes (1)

• The safety of ScTIL210

  To assess if the ScTIL210 product will be safe to the subjects, as assessed by the incidence of treatment-related adverse events, in the treatment of malignant solid tumors.

  24 weeks post infusion

Secondary Outcomes (2)

• The in vivo dynamic variation of reinfused ScTIL210

  24 weeks post infusion

• The efficacy of ScTIL210 in the treatment of malignant solid tumors

  24 weeks post infusion

Study Arms (1)

ScTIL210

EXPERIMENTAL

This trial is designed single arm. All the subjects enrolled will receive the experimental intervention, ScTIL210(Super circulating tumor infiltrating lymphocytes).

Biological: Super circulating tumor infiltrating lymphocytes(ScTIL)

Interventions

Super circulating tumor infiltrating lymphocytes(ScTIL) BIOLOGICAL

Peripheral blood mononuclear cells (PBMCs) are used for cell preparation. PD-1(programmed death 1) positive T cells are isolated from peripheral blood by blood cell apheresis method and transduced with lentivirus loaded with "enhanced receptor" and "superamplification factor". The obtained ScTIL is used for one-time intravenous infusion.

ScTIL210

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• When patients meet ALL of the following requirements, they will be eligible to be recruited, at their own wills, to participate in the clinical study.
• Age ≥ 18 years old and ≤ 75 years old, regardless of gender;
• An expected survival duration of longer than 3 months;
• Patients with malignant solid tumor as confirmed by histology or cytology who failed in their prior standard therapies , or there is no recommended standard treatment, or a standard treatment is not applicable at this time;
• The proportion of PD-1 positive T lymphocytes to the total T lymphocytes is ≥ 18%. For patients who received PD-1 monoclonal antibody treatment within 4 weeks before screening, the proportion of PD-1 positive T to the total T lymphocytes is ≥ 12%;
• In accordance to RECIST version 1.1, there is at least one evaluable tumor focus for dose escalation phase; or there is at least one measurable tumor focus for dose expansion stage;
• ECOG physical status score of between 0 to 1;
• Sufficient bone marrow and organ function; Blood system:no transfusion or hematopoietic stimulating factor treatment within 14 days; Neutrophil count (ANC): ≥ 1.5 × 109/L; Platelet (PLT): ≥ 75 × 109/L; Hemoglobin (HB): ≥ 90 g/L; Absolute lymphocyte count (lym): ≥60% of the lower limit of normal range; Lymphocyte subsets:Percentage of B lymphocyte (CD19+) to the total lymphocyte of ≥9%； Liver function Total bilirubin (TBIL) : ≤ 1.5 × ULN Alanine aminotransferase (ALT): ≤ 3 × ULN; for patients with liver metastasis or liver cancer: ≤ 5 × ULN Aspartate aminotransferase (AST)： ≤ 3 × ULN; for patients with liver metastasis or liver cancer: ≤ 5 × ULN Renal function：Creatinine ≤ 1.5 × ULN Coagulation function：Activated partial thromboplastin time (APTT) ≤ 1.5 × ULN ；International normalized ratio (INR) ≤ 1.5 × ULN
• Eligible fertile patients (male and female) must agree to use reliable contraceptive methods (hormonal or barrier method or abstinence, etc.) with their partners during the trial and at least 90 days after the last medication; women of childbearing age (as defined in Appendix 8) must have a negative blood or urine pregnancy test within 7 days before the first use of the study drug;
• The subjects should be informed of the study before the trial and sign the written informed consent voluntarily.

You may not qualify if:

• When a patient has one of the following conditions, he or she will not be eligible to be recruited to the clinical study.
• Received chemotherapy, radiotherapy, biological therapy, endocrine therapy, immunotherapy, traditional chinese medicine with anti-tumor indications and other anti-tumor treatments within 2 weeks before apheresis procedure, except for the following items:
• Nitrosourea or mitomycin C treatment was within 6 weeks before apheresis;
• Oral administration of fluorouracil and small molecule targeted drugs was one week before apheresis.
• Received other unlisted clinical research drugs or treatments within 4 weeks before ;
• Major organ surgery (excluding puncture biopsy) or significant trauma occurred within 4 weeks before apheresis, or a surgery was scheduled during the trial period;
• Received systemic corticosteroids (prednisone \> 10mg/day or equivalent dose of the similar drugs) or other immunosuppressants within 14 days before apheresis; Except for the following: topical, ocular, intra articular, nasal and inhaled glucocorticoids; short-term use of glucocorticoids for preventive treatment (e.g., prevention of contrast media allergy);
• Received immunomodulatory drugs, including but not limited to thymosin, interleukin-2, interferon, etc. within 14 days apheresis;
• Received live attenuated vaccine within 4 weeks before apheresis;
• The adverse reactions from previous anti-tumor therapy have not yet restored to CTCAE 5.0 grade evaluation of ≤1 (except for the toxicity without safety risk as judged by researchers such as alopecia).
• Central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence indicating that the central nervous system metastasis or meningeal metastasis has not been controlled, as judged by researcher inappropriate to be recruited to the study;
• Patients with active infection within one week before apheresis and a systemic anti-infection treatment is essential at this time;
• History of immunodeficiency, including positive HIV antibody test;
• Hepatitis B (HBsAg positive and/or a positive hepatitis C antibody and/or a positive treponema pallidum antibody;
• Patients with progressive interstitial pneumonitis;

Sponsors & Collaborators

• Shanghai East Hospital: lead

Study Sites (2)

Shanghai East Hospital

Shanghai, Shanghai Municipality, 200126, China

RECRUITING

Shanghai Zhongshan Hospital Affiliated to Fudan University

Shanghai, Shanghai Municipality, China

RECRUITING

Study Officials

• Jin Li, Ph.D.

  Shanghai Oriental Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Jin Li, MD,PhD

CONTACT

+86; lijin@csco.org.cn

Junli Xue, MD,PhD

CONTACT

+86; 13764694939@163.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 18, 2020
• First Posted: October 1, 2020
• Study Start: October 15, 2020
• Primary Completion: December 1, 2023
• Study Completion: December 1, 2024
• Last Updated: April 12, 2023

Record last verified: 2023-04

Locations

CN (2)