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OncoMatch/Clinical Trials/NCT06251973

A Study of agenT-797 in Combination With Botensilimab, Balstilimab, Ramucirumab, and Paclitaxel for People With Esophageal, Gastric, or Gastro-esophageal Junction Cancer

Is NCT06251973 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments for metastatic esophageal carcinoma.

Phase 2RecruitingMemorial Sloan Kettering Cancer CenterNCT06251973Data as of May 2026

Treatment: AgenT-797 · Botensilimab · Balstilimab · Ramucirumab · PaclitaxelParticipants will receive study treatment with agenT-797, botensilimab, balstilimab, ramucirumab, and paclitaxel. When participants start each agent will depend on how their disease is affecting them.

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Extracted eligibility criteria

Cancer type

Esophageal Carcinoma

Gastric Cancer

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 1 prior line
Min 1 prior line

Must have received: systemic therapy — metastatic

Disease progression on one prior line of therapy for metastatic disease. Patients with previously untreated advanced unresectable or metastatic disease may be included if disease progressed or recurred during neoadjuvant or adjuvant therapy or within 6 months of completion of those treatments.

Cannot have received: VEGFR inhibitor (ramucirumab)

Received prior therapy with ramucirumab at any time

Cannot have received: taxane (paclitaxel, docetaxel)

Exception: within 6 month of study enrollment

Received paclitaxel or docetaxel-based therapy within 6 month of study enrollment

Cannot have received: anti-PD-1 therapy

Exception: prior grade >3 immune related adverse event due to anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA4 therapy at any time

Had a prior grade >3 immune related adverse event due to anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA4 therapy at any time

Lab requirements

Blood counts

absolute neutrophil count: ≥1000/mcl; platelets: ≥90,000/mcl; hemoglobin: ≥8 g/dl

Kidney function

serum creatinine: ≤1.5x uln

Liver function

serum total bilirubin: ≤1.5x uln or direct bilirubin ≤uln for subjects with total bilirubin levels >1.5x uln, except patients with gilbert's disease (≤3x uln); ast and alt: ≤2.5x uln; albumin: ≥3 mg/dl

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities) · Basking Ridge, New Jersey
  • Memorial Sloan Kettering Monmouth (Limited Protocol Activities) · Middletown, New Jersey
  • Memorial Sloan Kettering Bergen (Limited Protocol Activities) · Montvale, New Jersey
  • Memorial Sloan Kettering Suffolk-Commack (Limited protocol activities) · Commack, New York
  • Memorial Sloan Kettering Westchester (Limited Protocol Activities) · Harrison, New York

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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