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NCT Number: NCT06088472

TIL Injection for the Treatment of Metastatic or Recurrent Solid Tumors

This is a single-center, single-arm phase I clinical trial.The study process was divided into: screening period, sampling and production period, NMA-LD chemotherapy , treatment and observation period, and follow-up period.

Recruiting

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Key information

Conditions

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

The Affiliated Hospital of Xuzhou Medical University

Xuzhou, Jiangsu, 221000, China

Location status: Recruiting

Location contact

Zhengxiang Han

PRINCIPAL_INVESTIGATOR

Zhengxiang Han, PHD

CONTACT

[email protected]

+86 18052268612

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. Voluntarily participate in the study, sign the informed consent form, and be willing and able to follow the study protocol ;
  • 2.Must have a confirmed diagnosis of malignancy of their receptive histologies or cytologies: unresectable recurrent or metastatic solid tumor;
  • 3.At least one resectable lesion (preferably superficial metastatic lymph nodes) that has not been treated with radiation and has not received other local therapies, and at least tissue blocks with a volume of≥0.5 cubic centimeter (either of single lesion origin or multiple lesions combined) can be isolated for the preparation of autologous tumor-infiltrating lymphocytes. Minimally invasive treatment where possible;

Exclusion criteria

  • 1. Patients who have symptomatic and/or untreated CNS metastases (Except stable brain metastases, no medication required within 3 months, no hormone dependence);
  • 2.The patient who has any active autoimmune disease, history of autoimmune disease, need for systemic steroid hormones or a condition requiring immunosuppressive drug therapy (>10 mg/day of prednisone or equivalent hormone) within 14 days before lymphocyte depletion chemotherapy;
  • 3. Arterial/venous thrombotic events within 6 months prior to enrollment, such as: cerebrovascular accident, deep vein thrombosis and pulmonary embolism occurring;
  • 4.Active infections requiring treatment with systemic anti-infectives (except for topical antibiotics); or those with unexplained fever > 38.5℃ occurring during the screening period, except for tumor fever;
  • 5. Patients who have refractory or intractable epilepsy, hydrops abdominis, active gastrointestinal bleeding or IL-2 contraindications;
  • 6. Patients who have received allogeneic bone marrow transplantation or an organ allograft;
  • 7.Patients who have a history of hypersensitivity to any component or excipient of study drugs: autologous tumor infiltrating lymphocytes, cyclophosphamide, fludarabine, IL-2, dimethyl sulfoxide (DMSO), human serum albumin (HSA), dextran-40 and antibiotics (beta lactam antibiotics, gentamicin);

Treatment and study plan

TIL injection

Biological

Autologous tumor infiltrating lymphocyte injection

Primary outcomes

  1. Incidence and severity of adverse events per CTCAE 5.0

    Time frame: From TIL infusion to the 24th week

    To characterize the safety profile of autologous TIL injection (GT101) in patients with relapsed/metastatic advanced solid tumor as measured by the incidence and severity of adverse events per CTCAE 5.0

Secondary outcomes

  1. Objective response rate (ORR)

    Time frame: Up to 24 months post infusion

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

  2. Disease control rate (DCR)

    Time frame: Up to 24 months post infusion

    To evaluate the percentage of participants that achieved partial response (PR), complete response (CR), or stable disease (SD) after treatment among total number of evaluable patients.

  3. Progression-free survival (PFS)

    Time frame: Up to 24 months post infusion

    To evaluate the time from the date of TIL infusion until disease progression per RECIST v1.1 and iRECIST as assessed by the investigator or death due to any cause.

  4. Duration of Response (DoR)

    Time frame: Up to 24 months post infusion

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

  5. Overall survival (OS)

    Time frame: From the date of TIL infusion to date of death due to any cause, or up to 24 months post infusion (whichever occurs first)

    To evaluate the time from the date of TIL infusion to death due to any cause.

Study contacts

Contact information is provided by the study sponsor or research team.

Zhengxiang Han, PHD

CONTACT

[email protected]

+86 18052268612

Sponsors and collaborators

Lead sponsor

Grit Biotechnology

Industry

Collaborators

  • The Affiliated Hospital of Xuzhou Medical University

Registry information

Official study title

A Single-arm Phase I Clinical Study of TIL Injection for the Treatment of Metastatic or Recurrent Solid Tumors

Important dates

Study start
2021
Primary completion
2027
Study completion
2027
First posted
Oct 18, 2023
Registry last updated
Sep 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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