Autologous Tumor Infiltrating Lymphocytes (GT101 Injection) in Patients with Recurrent or Metastatic Cervical Cancer

Grit Biotechnology

Status and phase

Enrolling

Phase 2

Conditions

Adult

Treatments

Biological: GT101 injection

Drug: Gemcitabine injection

Study type

Interventional

Funder types

Industry

Identifiers

NCT06241781

GT-CD-CHN-101-02

Details and patient eligibility

About

This is a Phase II, multicenter, open-label, randomized, parallel group, treatment study to assess the efficacy and safety of Autologous Tumor Infiltrating Lymphocytes (GT101 injection) compared with Gemcitabine in participants with recurrent or metastatic cervical cancer.

Enrollment

83 estimated patients

Sex

Female

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

1. The Patients (or legally authorized representative) Patients (or legally authorized representative) must have the ability to understand the requirements of the study, have provided written informed consent as evidenced by signature on an informed consent form (ICF) approved by an Institutional Review Board/Independent Ethics Committee (IRB/IEC) ,must have the ability to understand the requirements of the study);
1. The patient must be 18 to 70 years of age at the time of consent;
1. Must have a confirmed diagnosis of malignancy of their receptive histologies or cytology: unresectable recurrent or metastatic cervical carcinomas and previously received≥ 1 prior systemic therapy;
1. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1;
1. Expected survival time of ≥ 12 weeks;
1. Adequate normal organ and marrow function;
1. Before tumor resection, the confirmatory imaging of disease progress since last treatment should be documented.
8.Patients must have measurable disease measured by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria (in addition to the resected lesion).

Exclusion criteria

1.Patients with uncontrollable tumor-related pain as judged by the investigator; participants requiring painkiller must already have had a stable pain management options at the time of study entry; symptomatic lesions suitable for palliative radiotherapy should be completed prior to study entry;
2.Patients who have psychiatric disorders, alcohol, drug or substance abuse;
3.Women who are pregnant or breastfeeding, or planning to become pregnant within 1 year after cell infusion;
4.Participate in other clinical trials within 4 weeks prior to screening, or planning to participate in this study and other clinical trials at the same time;
5.Any other conditions that would make the patient unsuitable candidate for the study at the discretion of the investigator.