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Not Yet RecruitingNCT07371871

A Prospective, Single-arm, Exploratory Study of Trifluridine/Tipiracil (TAS-102) Combined With Apatinib as Third-line Therapy for Advanced Gastric Cancer

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Anhui Provincial Cancer Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy and safety of trifluridine/tipiracil (TAS-102) combined with apatinib as third-line therapy for advanced gastric cancer

Conditions

Interventions

TypeNameDescription
DRUGTrifluridine/Tipiracil (TAS-102) combined with ApatinibTAS-102: 35 mg/m2/dose, taken orally within 1 hour after breakfast and dinner, twice daily, on days 1-5 of each cycle, followed by a 9-day drug-free interval, with 28 days constituting one cycle. Apatinib: 500 mg/dose, once daily, administered continuously for 5 days followed by a 2-day break, with 28 days as one cycle. Imaging evaluation should be performed every 2-3 cycles until disease progression or intolerance occurs.

Timeline

Start date
2026-01-08
Primary completion
2027-12-31
Completion
2028-12-31
First posted
2026-01-28
Last updated
2026-01-28

Source: ClinicalTrials.gov record NCT07371871. Inclusion in this directory is not an endorsement.

A Prospective, Single-arm, Exploratory Study of Trifluridine/Tipiracil (TAS-102) Combined With Apatinib as Third-line Th (NCT07371871) · Clinical Trials Directory