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TAS-102, Regorafenib , Fruquintinib

Suzhou Suncadia Biopharmaceuticals Co., Ltd. · Phase 3 active Small molecule

TAS-102, Regorafenib , Fruquintinib is a Nucleoside analog, Multi-kinase inhibitor, VEGFR2 inhibitor Small molecule drug developed by Suzhou Suncadia Biopharmaceuticals Co., Ltd.. It is currently in Phase 3 development for Metastatic colorectal cancer, Gastrointestinal stromal tumor, Colorectal cancer.

TAS-102 is a nucleoside analog that inhibits thymidylate synthase, leading to DNA damage in cancer cells. Regorafenib is a multi-kinase inhibitor that targets angiogenic, stromal, and tumor cells. Fruquintinib is a potent and highly selective inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2).

TAS-102 is a nucleoside analog that inhibits thymidylate synthase, leading to DNA damage in cancer cells. Regorafenib is a multi-kinase inhibitor that targets angiogenic, stromal, and tumor cells. Fruquintinib is a potent and highly selective inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2). Used for Metastatic colorectal cancer, Gastrointestinal stromal tumor, Colorectal cancer.

At a glance

Generic nameTAS-102, Regorafenib , Fruquintinib
SponsorSuzhou Suncadia Biopharmaceuticals Co., Ltd.
Drug classNucleoside analog, Multi-kinase inhibitor, VEGFR2 inhibitor
TargetThymidylate synthase, VEGFR2
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

TAS-102 works by incorporating into DNA and causing DNA damage, which triggers cell death in cancer cells. Regorafenib targets multiple kinases involved in tumor growth and angiogenesis, leading to reduced tumor size and progression. Fruquintinib selectively inhibits VEGFR2, which is crucial for tumor angiogenesis and growth.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about TAS-102, Regorafenib , Fruquintinib

What is TAS-102, Regorafenib , Fruquintinib?

TAS-102, Regorafenib , Fruquintinib is a Nucleoside analog, Multi-kinase inhibitor, VEGFR2 inhibitor drug developed by Suzhou Suncadia Biopharmaceuticals Co., Ltd., indicated for Metastatic colorectal cancer, Gastrointestinal stromal tumor, Colorectal cancer.

How does TAS-102, Regorafenib , Fruquintinib work?

TAS-102 is a nucleoside analog that inhibits thymidylate synthase, leading to DNA damage in cancer cells. Regorafenib is a multi-kinase inhibitor that targets angiogenic, stromal, and tumor cells. Fruquintinib is a potent and highly selective inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2).

What is TAS-102, Regorafenib , Fruquintinib used for?

TAS-102, Regorafenib , Fruquintinib is indicated for Metastatic colorectal cancer, Gastrointestinal stromal tumor, Colorectal cancer.

Who makes TAS-102, Regorafenib , Fruquintinib?

TAS-102, Regorafenib , Fruquintinib is developed by Suzhou Suncadia Biopharmaceuticals Co., Ltd. (see full Suzhou Suncadia Biopharmaceuticals Co., Ltd. pipeline at /company/suzhou-suncadia-biopharmaceuticals-co-ltd).

What drug class is TAS-102, Regorafenib , Fruquintinib in?

TAS-102, Regorafenib , Fruquintinib belongs to the Nucleoside analog, Multi-kinase inhibitor, VEGFR2 inhibitor class. See all Nucleoside analog, Multi-kinase inhibitor, VEGFR2 inhibitor drugs at /class/nucleoside-analog-multi-kinase-inhibitor-vegfr2-inhibitor.

What development phase is TAS-102, Regorafenib , Fruquintinib in?

TAS-102, Regorafenib , Fruquintinib is in Phase 3.

What are the side effects of TAS-102, Regorafenib , Fruquintinib?

Common side effects of TAS-102, Regorafenib , Fruquintinib include Diarrhea, Fatigue, Hypertension, Hand-foot syndrome, Rash.

What does TAS-102, Regorafenib , Fruquintinib target?

TAS-102, Regorafenib , Fruquintinib targets Thymidylate synthase, VEGFR2 and is a Nucleoside analog, Multi-kinase inhibitor, VEGFR2 inhibitor.

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