Clin2
NCT06340711Possibly a fitRecruiting

Gene therapy plus Keytruda for advanced stomach or esophageal cancer

Esophageal AdenocarcinomaGastric AdenocarcinomaGastroesophageal Junction Adenocarcinoma

Treatments studied

Part of Cancer, Digestive system clinical trials.

This study tests a new type of gene therapy (OBP-301) injected directly into the tumor, combined with the immunotherapy drug Keytruda (pembrolizumab), for people with advanced stomach, junction, or esophageal cancer. Researchers want to see if this combination can help when standard treatments have stopped working.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
27 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have advanced stomach, gastroesophageal junction, or esophageal cancer that can be injected into with a needle, with a tumor at least 1 cm in size.
  • Your tumor must have been tested for PD-L1 (a protein affecting immune response), and your doctor should know your score.
  • If your PD-L1 score is above 1: you must have already tried at least one line of standard treatment that included an immunotherapy drug (a PD-1 or PD-L1 inhibitor), and your cancer must have progressed during or within 3 months of finishing that treatment.
  • If your PD-L1 score is below 1: you must NOT have had prior immunotherapy, but you must have received at least one line of chemotherapy or other standard therapy for advanced disease.
  • You cannot have an active autoimmune disease that needed strong immune-suppressing drugs in the last 2 years, cannot be on high-dose steroids (more than 20 mg prednisone daily) within the last week, and cannot have had severe immune side effects from prior immunotherapy.
  • No active brain metastases, no uncontrolled infections, no HIV/hepatitis B or C, no other progressing cancer within 3 years, and no organ transplant.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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