Drugs / TAS-114
last change Dec 2018 re-read 9 days ago

TAS-114

Developed for
neoplasm · cancer · non-small cell lung carcinoma
Investigated by
Taiho Oncology, Inc. · Quintiles, Inc. · Taiho Pharmaceutical Co., Ltd.

Trials 3

201320142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 13 trials
Phase 1 NCT02454062 Mar 2013 → Dec 2016 neoplasm Taiho Oncology, Inc. Completed No outcome recorded
Phase 1 NCT02025803 Nov 2012 → Jul 2017 neoplasm Taiho Oncology, Inc. Completed No outcome recorded
Phase 1 NCT01610479 Jun 2012 → Feb 2017 cancer Taiho Pharmaceutical Co., Ltd. Completed No outcome recorded
Comparator or background therapy1 trial
Phase 2 NCT02855125 Comparator Aug 2016 → Sep 2017 non-small cell lung carcinoma Taiho Oncology, Inc. Completed No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2018-04-13 Taiho Oncology, Inc. Results Taiho Oncology Presents Data on LONSURF® (trifluridine and tipiracil) and Key Investigational Compounds at the 109th Annual Meeting of the American Association for Cancer Research taihooncology.com ↗
The study found that TAS-114 combined with capecitabine (at 30% of its standard dose) achieved an equivalently efficacious 5-fluorouracil (5-FU) exposure as the standard capecitabine dose alone, with acceptable safety and preliminary efficacy in patients with advanced solid tumors.

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as TAS-114 ClinicalTrials.gov intervention name — accepted as the source's own label NCT02025803 ↗
3

NCT02454062 ↗

NCT02855125 ↗

NCT01610479 ↗

Action Inhibit “novel dUTPase inhibitor” PMID 30511200 ↗ Dec 2018
Route Oral “TAS-114 and S-1 were concurrently administered orally under fasting conditions” PMID 30511200 ↗ Dec 2018