RecruitingPhase 2NCT05620628

Ph2 Study of Savolitinib and Durvalumab (MEDI4736) Combination in Advanced MET Amplified Gastric Cancer(VIKTORY-2)


Sponsor

Jeeyun Lee

Enrollment

25 participants

Start Date

Jan 5, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

For patients who failed primary chemotherapy with MET amplification, The efficacy and safety of the chemotherapy are evaluated by using dervalumab and saboritinib in combination.


Eligibility

Min Age: 19 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of two drugs — savolitinib (which blocks a cancer-driving protein called MET) and durvalumab (an immunotherapy drug) — in people with advanced stomach cancer that has a specific genetic amplification in the MET gene. **You may be eligible if...** - You are 19 or older with advanced gastric (stomach) cancer that has progressed during or after 1–2 prior chemotherapy regimens - Your cancer has been shown to have MET gene amplification on a genetic test (copy number 4 or higher) - You have at least one measurable tumor on imaging - Your general health score is 0–1 and life expectancy is at least 3 months - Your body weight is over 30 kg **You may NOT be eligible if...** - Your cancer does not have MET amplification - You have not had a sufficient washout period from prior therapies - Your organ function does not meet the required minimums - You have serious uncontrolled health conditions 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.

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Interventions

DRUGDurvalumab

Durvalumab will be administered at 1500mg every 4 weeks from cycles 1 day 1.

DRUGSavolitinib

Savoritinib 600mg will be administered orally a day for 28 days as one cycle.


Locations(1)

Samsung Medical Center

Seoul, South Korea

View Full Details on ClinicalTrials.gov

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NCT05620628


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