Clinical Trial on the Safety, Tolerance and Preliminary Efficacy of XH001 Injection Combined With Neoantigen Vaccine-induced Tumor-specific T-cell Injection in Advanced Gastric Cancer

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-70
SponsorJia Wei

About this trial

The goal of this clinical trial is to learn the safety of tumor neoantigen vaccine combined with neoantigen vaccine induced T-cell in treating advanced gastric cancer in adults. It will also learn if the combined treatment works to treat advanced gastric cancer.

The main questions it aims to answer are:

What medical problems do participants have when using the combined treatment? Does tumor neoantigen vaccine combined with neoantigen vaccine induced T-cell eliminate or shrink the tumor, and can it prolong the patient's survival period?

Eligibility criteria

Qualifiers

Provision of signed and dated informed consent form.

Aged between 18 and 70 years old, male or female.

Advanced gastric cancer that has been diagnosed by histological and/or cellular pathology, and which has failed to respond to second-line standard treatment or is intolerant to it, or is not suitable for standard treatment at this stage.

According to the RECIST 1.1 criteria for evaluating the efficacy of solid tumors, there must be at least one measurable lesion as the target lesion for efficacy evaluation. The total diameter of the overall tumor lesion (excluding bone metastases) should be ≤ 100mm, and the diameter of a single tumor lesion should be ≤ 30mm. If the lesion that has received local treatment (radiotherapy, ablation, vascular intervention, etc.) is the only lesion, then there must be clear imaging evidence of disease progression for this lesion.

Disqualifiers

Requires long-term systemic administration of antiallergic drugs, or has severe hypersensitivity reactions (≥Grade 3) to XH001 injection and/or any of its excipients.

Central nervous system metastases with symptoms and without prior treatment, and/or meningeal metastases.

Having received immunomodulatory drug therapy within 2 weeks prior to the first administration day (D1) of XH001 injection.

Suffer from skin diseases that may prevent the intradermal injection from reaching the target area (such as psoriasis).

Trial design

Treatments tested in this trial

  • XH001 Injection
  • Tumor vaccine-induced specific T-cell injection

Treatment groups

18 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Jia Wei

Lead sponsor

The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Sponsor institution

NeoCura

Collaborator