New drug cocktail shows promise for tough stomach cancer
NCT ID NCT03223376
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether adding fruquintinib to standard chemotherapy (paclitaxel) helps people with advanced stomach cancer live longer. It included 703 patients whose cancer had worsened after initial treatment. The goal was to see if the combination improves survival and slows cancer growth.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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703 people
The number who actually took part.
- Started
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Oct 2017
- Finished
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Sep 2022
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Signed informed consent * Histologically or cytologically confirmed gastric or gastroesophageal junction adenocarcinoma * Metastatic disease or locally advanced, unresectable disease * Disease progression during or within 4 months after the last dose of the first-line therapy (with platinum/fluoropyrimidine ) * Adequate hepatic, renal, heart, and hematologic functions * At least one measurable lesion (larger than 10 mm in diameter by spiral CT scan) * Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedure * Good performance status Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0 to 1 Exclusion Criteria: * Pregnant or lactating women * Any factors that influence the usage of oral administration * Evidence of CNS metastasis * Intercurrence with one of the following: non-controlled hypertension, coronary artery disease, arrhythmia and heart failure * Abuse of alcohol or drugs * Less than 4 weeks from the last clinical trial * Previous treatment with VEGFR inhibition * Disability of serious uncontrolled intercurrence infection * Proteinuria ≥ 2+ (1.0g/24hr) * Have evidence or a history of bleeding tendency within two months of the enrollment randomization, regardless of seriousness * Within 12 months before the first treatment occurs artery/venous thromboembolic events, such as cerebral vascular accident (including transient ischemic attack) etc. * Within 6 months before the first treatment occurs acute myocardial infarction, acute coronary syndrome or CABG * Bone fracture or wounds that was not cured for a long time * Coagulation dysfunction, hemorrhagic tendency or receiving anticoagulant Therapy * The tumor invades a large vessel structure, such as the pulmonary artery, superior vena cava, or inferior vena cava
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Huchison Medi Pharma Investigational site
Nanjing, Jiangsu, 210000, China
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Hutchison Medi Pharma Invesigational sites
Hefei, Anhui, 230000, China
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Hutchison Medi Pharma Investigational Site
Guangzhou, Guangdong, 510030, China
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Hutchison Medi Pharma Investigational site
Harbin, Heilongjiang, 150081, China
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Hutchison Medi Pharma Investigational site
Shanghai, 200125, China
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Hutchison Medi Pharma Investigational sites
Hangzhou, Zhejiang, 310000, China
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Hutchison Medi Pharma Investigational sites
Beijing, 100142, China
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Other studies related to the condition(s) this trial covers.
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