Safety and Efficacy of Metabolically Armed Tumor-lnfiltrating Lymphocytes (Meta10-TIL) for the Treatment of Advanced Solid Tumors

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age19-70
SponsorAnhui Provincial Hospital

About this trial

A Study of Metabolically Armed Tumor-Infiltrating Lymphocytes (Meta10-TIL) Therapy for Patients With Advanced Solid Tumors

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

The patient or his/her guardian voluntarily signed the informed consent;

Age >18 years and ≤70 years, male or female;

Recurrent/metastatic/persistent cervical cancer with prior failure (disease progression or intolerable toxicity) of at least 1 but no more than 3 systemic therapies;

Systemic therapy is defined as any chemotherapy or multi-drug combination chemotherapy regimen recommended by guidelines used for cervical cancer;

Disqualifiers

Presence of bone metastases only.

Active central nervous system (CNS) metastases (except for stable brain metastases not requiring medication or steroid dependence for ≥3 months).

Use of Chinese herbal medicine or botanical drugs with antitumor indications within 1 week before preconditioning.

Systemic corticosteroid therapy (≥10 mg/day prednisone or equivalent) or other immunosuppressive drugs within 2 weeks before preconditioning (excluding inhaled, topical, or physiological replacement therapy).

Trial design

Design model

Sequential

Treatments tested in this trial

  • Metabolically Armed TIL cells

    Drug

    Each subject receive metabolically armed TIL cells by intravenous infusion.

Treatment groups

36 Participants
are divided into 1 treatment group
Group A: Administration of Metabolically Armed tumor-infiltrating lymphocytes(Meta10-TIL)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Adverse Events(AEs)

To characterize the safety profile of Meta10-TIL in patients with advanced solid tumor as assessed by incidence of adverse events. Adverse events will be graded by the National Cancer Institute Common Terminology Criteria for Adverse Events(NCI CTCAE) version 5.0.

Time frame
1 year post Meta10-TIL infusion

Secondary outcomes

1

Objective response rate(ORR)

To evaluate the proportion of participants who have a confirmed partial response (PR) and complete response (CR) per RECIST v1.1 as assessed by the investigator.

Time frame
1 year post Meta10-TIL infusion
2

Overall survival(OS)

OS is measured from the date of the infusion of Meta10-TIL to the date of the subjects' death.

Time frame
1year post Meta10-TIL infusion
3

Duration of Response(DOR)

To evaluate the duration from the time that criteria are met for CR or PR per RECIST v1.1 as assessed by the investigator until disease progression or death due to any cause.

Time frame
1 year post Meta10-TIL infusion
4

Progression-free survival(PFS)

The time from the start of Meta10-TIL treatment for the subjects to the first disease progression or death for any reason.

Time frame
1 year post Meta10-TIL infusion

Other outcomes

Sponsors and contacts

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Anhui Provincial Hospital

Lead sponsor

Leman Biotech Co., Ltd.

Collaborator