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Clinical Trial Summary

This is a single-arm, non-randomised study including patients with EBER positive nasopharyngeal carcinoma with recurrent or metastatic disease not amenable to curative treatment, who have received at least 1 regimen of platinum containing chemotherapy.


Clinical Trial Description

HYPOTHESIS Given the favourable activity of fluoropyrimidines (5Fluorouracil) which inhibit thymidylate synthase (TS) in nasopharyngeal carcinoma, the investigators hypothesized that TAS-102 may demonstrate efficacy in NPC through targeting TS as well as an additional mechanism of incorporating trifluridine triphosphate into DNA. OBJECTIVES OF TRIAL 1. To determine the clinical efficacy of TAS-102 in recurrent and metastatic NPC 2. To assess the safety and tolerability of TAS-102 in the study population of R/M NPC 3. To study the pharmacokinetics of TAS-102 in the study population of R/M NPC 4. To study potential predictive biomarkers for clinical benefit from TAS-102 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04627961
Study type Interventional
Source National University Hospital, Singapore
Contact Boon Cher Goh
Phone 6779 5555
Email phcgbc@nus.edu.sg
Status Recruiting
Phase Phase 2
Start date August 26, 2020
Completion date October 2024

See also
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