NCT05447234Not yet recruitingEarly phase 1
TCRx_T Cells for Advanced or Recurrent Gastric/Gastroesophageal Junction Cancer After Failure of First Chemotherapy
Exploratory Clinical Study of TCRx_T Cells in the Treatment of Advanced or Recurrent Gastric/Gastroesophageal Junction Cancer After Failure of First Chemotherapy
Source: ClinicalTrials.gov · Last updated 16 Feb 2023 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
To observe and determine the safety, tolerability, cellular pharmacokinetics and efficacy of TCRx T cells in patients with advanced or recurrent gastric/gastroesophageal junction cancer after failure of first chemotherapy.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Early phase 1
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- First submitted
- 3 Jul 2022
- Start date
- 1 Mar 2023
- Primary completion date
- 1 Mar 2026
- Lead sponsor
- Second Affiliated Hospital, Zhejiang University, School of Medicine
- Diseases
- Gastric and esophageal cancer
- NCT number
- NCT05447234
What you commit to
- Study type: Interventional · Early phase 1
- Planned participants: 50
- From 1 Mar 2023 to the primary completion date, 1 Mar 2026
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with previous non-gastric/gastroesophageal junction malignant tumor
- Any serious and/or unstable previous medical, psychiatric, or other circumstances that may affect subject safety, provide informed consent, or comply with research procedures
- Unable or unwilling to stop using illicit drugs for at least 14 days or drug half-life (whichever is longer) before and during the first study drug administration
- Treated with any of the following anticancer therapies: radiotherapy, tumor embolization or chemotherapy, immunotherapy, biological therapy within 14 days before the first dose; neoadjuvant chemotherapy or adjuvant chemotherapy must be at least 6 months before the start of the study Finish
- Any persistent toxicity greater than grade 1 and/or worsening in severity from prior anticancer therapy, except for alopecia
- Participate in a clinical trial of another investigational drug within 30 days prior to the start of the study
Other illness
- History of severe acute allergy
- There is an uncontrolled infection
- History of cerebrovascular accident within the past 6 months, including transient ischemic attack (TIA), pulmonary embolism or untreated deep vein thrombosis (DVT)
- History of one or more of the following cardiovascular diseases within the past 6 months: cardiac angioplasty or stenting, myocardial infarction, unstable angina, coronary artery bypass grafting, symptomatic peripheral vascular disease , NYHA type III or IV congestive heart failure
- Poor control of hypertension
- Evidence of active bleeding or bleeding tendency
- Clinically significant gastrointestinal abnormalities, such as bleeding, obstruction, and high risk of perforation
Lab values
- QT interval \>480ms
Other
- History or clinical evidence of central nervous system (CNS) metastasis or leptomeningeal carcinomatosis
- Grade 3 or 4 diarrhea
- Pregnant or lactating women
- Men or women planning to become pregnant within the next six months
Who the study is looking for
- Age 18-70 years old;
- Histologically confirmed advanced/locally advanced or metastatic gastric cancer at the stomach or gastroesophageal junction, progressed after first-line chemotherapy, or recurrence after gastric/gastroesophageal junction surgery combined with neoadjuvant/adjuvant chemotherapy
- Expected survival time ≥ 3 months
- Eastern Cooperative Oncology Group (ECOG) score 0-2
- According to the Response Evaluation Criteria for Solid Tumors (RECIST 1.1), at least one one-dimensional, measurable tumor (short-axis diameter greater than 1 cm)
- Normal bone marrow hematopoietic function: (leukocytes≥4000 cells/㎕, neutrophils≥1500 cells/㎕, platelet counts≥100000 cells/㎕)
- Normal liver and kidney function: serum bilirubin \<1.5mg/dl, AST (SGOT) and ALT (SGPT) \<2.5UNL, alkaline phosphatase \<5UNL; serum creatinine \<1.5mg/dl;
- Men and women must take appropriate contraceptive measures.
Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.