RecruitingPhase 2NCT07289997

Iparomlimab and Tuvonralimab Combined With Apatinib and Irinotecan Hydrochloride for the Treatment of Advanced Alpha-fetoprotein-producing Gastric Cancer (AFPGC)

Iparomlimab and Tuvonralimab Injection Combined With Apatinib and Irinotecan Hydrochloride for the Treatment of Advanced Alpha-fetoprotein-producing Gastric Cancer (AFPGC) That Progresses From First-line PD-1 Combined Chemotherapy, A Prospective, Single-arm, Phase II Clinical Study


Sponsor

Hebei Medical University Fourth Hospital

Enrollment

39 participants

Start Date

Sep 28, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study is a single-arm study aimed at evaluating the efficacy and safety of Iparomlimab and Tuvonralimab Injection combined with apatinib and irinotecan hydrochloride in the treatment of advanced alpha-fetoprotein gastric cancer (AFPGC) that progresses from first-line PD-1 combined with chemotherapy. The study enrolled patients with advanced gastric cancer and gastroesophageal junction cancer whose serum alpha-fetoprotein was greater than 20.0 ng/mL at the initial diagnosis and progressed after first-line PD-1 combined chemotherapy in a single center of the Fourth Hospital of Hebei Medical University. All patients underwent gastroscopy and were pathologically confirmed as Her-2 negative gastric adenocarcinoma, and had received PD-1 inhibitor treatment as the first-line treatment. Staged examinations include enhanced CT of the abdominal and pelvic cavities, plain CT scan of the chest, and color Doppler ultrasound of superficial lymph nodes. The enrolled patients received apalolitovolrelimab 5.0mg/kg, Q3W, d1; Apatinib mesylate, 0.25g, once daily; Irinotecan hydrochloride, 200mg/m², Q3W, d1. Combination therapy until the patient's disease progresses, or intolerable toxic and side effects occur, or until death or withdrawal of informed consent, or up to two years. The primary endpoint of the study was to assess the objective response rate (ORR) of combination therapy. Secondary endpoints included progression-free survival (PFS), disease control rate (DCR), overall survival (OS), and the incidence of adverse events, etc


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a combination of two immunotherapy drugs (iparomlimab and tuvonralimab) together with a targeted drug (apatinib) and a chemotherapy drug (irinotecan) in people with a rare, aggressive form of stomach or gastroesophageal junction cancer that produces high levels of a protein called alpha-fetoprotein (AFP). **You may be eligible if...** - You are 18 or older - You have been diagnosed with advanced, unresectable, or metastatic stomach or gastroesophageal junction cancer confirmed by biopsy - Your blood AFP level was above 20.0 ng/mL at diagnosis - You have at least one measurable tumor - Your cancer progressed during or after first-line treatment that included a PD-1 inhibitor and chemotherapy - You are in reasonably good physical condition (ECOG 0–1) - Your organs (kidneys, liver, blood) are functioning adequately **You may NOT be eligible if...** - Your cancer is HER2-positive - Your cancer is squamous cell or undifferentiated type - You have active autoimmune disease or other serious conditions that interfere with immunotherapy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGIparomlimab and Tuvonralimab Injection (QL1706)

1. Iparomlimab and Tuvonralimab Injection, 5.0mg/kg, Q3W, D1; 2. Apatinib, 0.25g, once daily, orally; Irinotecan, 200mg/m², Q3W, D1; Combination therapy until the patient's disease progresses, or intolerable toxic and side effects occur, or until death or withdrawal of informed consent, or up to two years.


Locations(1)

Hebei Medical University Fourth Hospital

Shijiazhuang, Hebei, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07289997


Related Trials