BGT007H Cells for the Treatment of Recurrent/Refractory Gastrointestinal Tumors

NCT06152757 | Recruiting Early Phase 1

• 1 other identifier: BR-BGT-003
• Study Type: interventional
• Target: 14
• Locations: 1 country
• Sites: 1

Brief Summary

This study is an exploratory single-arm, open, modified "3+3" dose escalation study with BGT007H injection. Approximately 11 to 14 subjects with recurrent/refractory gastrointestinal tumors will be enrolled to evaluate the safety of BGT007H injection. Four dose levels were designed for this study: 1.0×10\^8cells, 3.0×10\^8cells, 1.0×10\^9cells, and 3.0×10\^9cells. The primary objective of this study was to evaluate the safety, tolerability and pharmacokinetic profile of BGT007H cell therapy in patients with recurrent/refractory digestive tract tumors, to determine the maximum tolerated dose or the best effective dose, and to initially evaluate the effectiveness of BGT007H cell products.

Conditions

Gastrointestinal Tumors

Outcome Measures

Primary Outcomes (3)

• Dose-Limiting Toxicity (DLT)

  Incidence of adverse events defined as Dose-Limiting Toxicity (DLT).

  From the infusion (Day 0) to Day 28

• Maximum tolerated dose

  The maximum CAR-T dose that can be tolerated in the study.

  From the infusion (Day 0) to Day 28

• AE, SAE, AESI, CRS, ICANS, TEAE

  The incidence of adverse events (AE), serious adverse events (SAE), adverse events of special interest (AESI), cytokine release syndrome (CRS) immune cell associated neurotoxicity syndrome (ICANS) and treatment-emergent adverse events (TEAE).

  The day of leukapheresis to 12 months after infusion

Study Arms (1)

BGT007H injection

EXPERIMENTAL

Intravenous infusion

Biological: First dose; Biological: Second dose; Biological: The third dose; Biological: The fourth dose

Interventions

First dose BIOLOGICAL

1.0×10\^8cells,Intravenous infusion，1 subject is planned to be enrolled

BGT007H injection

Second dose BIOLOGICAL

3.0×10\^8cells,Intravenous infusion，3 subject is planned to be enrolled

BGT007H injection

The third dose BIOLOGICAL

1.0×10\^9cells,Intravenous infusion，3 subject is planned to be enrolled

BGT007H injection

The fourth dose BIOLOGICAL

3.0×10\^9cells,Intravenous infusion，3 subject is planned to be enrolled

BGT007H injection

Eligibility Criteria

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

You may qualify if:

• \. Resources sign written informed consent;
• , age ≥18, male and female can;
• \. Expected survival ≥3 months;
• \. The Eastern Cancer Collaboration (ECOG) physical status score was 0-1;
• \. Biopsy specimen or pathological wax section test (within 3 years before accepting the signed informed consent) : positive target test;
• \. According to RECISTv1.1 solid tumor evaluation criteria, there is at least one measurable lesion;
• \. Patients with advanced gastrointestinal tumors (esophageal cancer, gastric cancer, pancreatic cancer or colorectal cancer, etc.) who have been diagnosed by histology/cytology as having failed the standard of second-line or above treatment or are not suitable for/refuse to accept the standard treatment or cannot tolerate the standard treatment; The definition of intolerance: according to CTCAE V5.0, the occurrence of ≥Ⅳ hematological toxicity or ≥Ⅲ non-hematological toxicity or ≥Ⅱ damage to the heart, liver, kidney and other important organs during treatment; Treatment failure is defined as disease progression (PD) during treatment or recurrence after the end of treatment (including postoperative recurrence);
• , can establish monopexy or venous blood collection venous access, and there are no other contraindications for blood cell separation;
• , with adequate organ and bone marrow function;
• \. During the study period and for 6 months after the end of dosing, fertile subjects (both male and female) must use effective medical contraception. For female subjects of reproductive age, a pregnancy test should be performed within 72 hours before the first dose, and the result is negative.

You may not qualify if:

• \. Active central nervous system metastasis (except stable after treatment);
• , HIV positive, HBsAg positive simultaneously detected HBV DNA copy number positive (quantitative detection ≥1000cps/ml), HCV antibody positive and HCV RNA positive;
• , mental or mental illness can not cooperate with treatment and efficacy evaluation;
• \. Subjects with severe autoimmune diseases and long-term use of immunosuppressants;
• \. Active or uncontrollable infection requiring systemic treatment within 14 days prior to enrollment;
• \. Any unstable systemic disease (including but not limited to: Active infections (except local infections); Unstable angina pectoris Cerebral ischemia or cerebrovascular accident (within 6 months prior to screening) Myocardial infarction (within 6 months prior to screening) Congestive heart failure (New York Heart Association \[NYHA\] classification ≥Ⅲ; Severe arrhythmias requiring medical treatment; Have heart disease that requires treatment or uncontrolled hypertension after treatment (blood pressure \> 160mmHg/100mmHg);
• , combined with lung, brain, kidney and other important organ dysfunction;
• \. The subject has undergone major surgery or severe trauma within 4 weeks prior to receiving cell therapy, or is expected to undergo major surgery during the study period;
• \. Received any systemic chemotherapy, immunotherapy or small molecule targeted therapy within 1-2 weeks or 5 half-lives (whichever is shorter) before anapheresis;
• \. The subject currently has or has had other malignant tumors that cannot be cured within 3 years, except cervical cancer or basal cell carcinoma of the skin, and other malignant tumors with a disease-free survival of more than 5 years;
• , received chimeric antigen receptor modified T cells (including CAR-T, CTT-T) treatment within half a year;
• \. Combined graft-versus-host disease (GVHD)
• \. Subjects who were receiving systemic steroid therapy prior to screening and who were determined by the investigator to require long-term use of systemic steroid therapy during treatment (except for inhalation or topical use); And subjects treated with systemic steroids within 72 hours prior to cell transfusion (except for inhalation or topical use);
• \. Severe allergy or history of allergy;
• \. Subjects requiring anticoagulation therapy;

Sponsors & Collaborators

• BioSyngen Pte Ltd: lead
• The First Affiliated Hospital of Zhengzhou University: collaborator

Study Sites (1)

The First Affiliated Hospital of Zhengzhou University

Zhengzhou, Henan, China

RECRUITING

MeSH Terms

Conditions

Digestive System Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Digestive System Diseases

Study Officials

• Yi Zhang

  The First Affiliated Hospital of Zhengzhou University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Xinfeng Chen

CONTACT

0371-66295320; fengxinchen1985@163.com

Dan Wang

CONTACT

13383812031; wang.dan1002@163.com

Study Design

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

Study Record Dates

• First Submitted: November 22, 2023
• First Posted: December 1, 2023
• Study Start: October 9, 2023
• Primary Completion: July 19, 2025
• Study Completion (Estimated): July 19, 2027
• Last Updated: December 1, 2023

Record last verified: 2023-11

Locations

CN (1)