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Gemcitabine, Vinorelbine, Eribulin, or Utidelone

Sun Yat-sen University · Phase 3 active Small molecule

Gemcitabine, Vinorelbine, Eribulin, or Utidelone is a Chemotherapy combination (nucleoside analog, vinca alkaloid, microtubule inhibitor, microtubule stabilizer) Small molecule drug developed by Sun Yat-sen University. It is currently in Phase 3 development for Non-small cell lung cancer, Breast cancer, Gastric cancer.

This is a combination of three chemotherapy agents that work through different mechanisms to inhibit cancer cell division and promote apoptosis.

This is a combination of three chemotherapy agents that work through different mechanisms to inhibit cancer cell division and promote apoptosis. Used for Non-small cell lung cancer, Breast cancer, Gastric cancer.

At a glance

Generic nameGemcitabine, Vinorelbine, Eribulin, or Utidelone
SponsorSun Yat-sen University
Drug classChemotherapy combination (nucleoside analog, vinca alkaloid, microtubule inhibitor, microtubule stabilizer)
TargetMultiple: ribonucleotide reductase, microtubules, DNA synthesis
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Gemcitabine is a nucleoside analog that inhibits ribonucleotide reductase and DNA synthesis. Vinorelbine is a semi-synthetic vinca alkaloid that disrupts microtubule formation and mitotic spindle function. Eribulin is a microtubule dynamics inhibitor that suppresses microtubule growth. Utidelone is a novel microtubule-stabilizing agent. Together, these agents target multiple pathways of cancer cell proliferation.

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 Gemcitabine, Vinorelbine, Eribulin, or Utidelone

What is Gemcitabine, Vinorelbine, Eribulin, or Utidelone?

Gemcitabine, Vinorelbine, Eribulin, or Utidelone is a Chemotherapy combination (nucleoside analog, vinca alkaloid, microtubule inhibitor, microtubule stabilizer) drug developed by Sun Yat-sen University, indicated for Non-small cell lung cancer, Breast cancer, Gastric cancer.

How does Gemcitabine, Vinorelbine, Eribulin, or Utidelone work?

This is a combination of three chemotherapy agents that work through different mechanisms to inhibit cancer cell division and promote apoptosis.

What is Gemcitabine, Vinorelbine, Eribulin, or Utidelone used for?

Gemcitabine, Vinorelbine, Eribulin, or Utidelone is indicated for Non-small cell lung cancer, Breast cancer, Gastric cancer, Other solid tumors (phase 3 evaluation).

Who makes Gemcitabine, Vinorelbine, Eribulin, or Utidelone?

Gemcitabine, Vinorelbine, Eribulin, or Utidelone is developed by Sun Yat-sen University (see full Sun Yat-sen University pipeline at /company/sun-yat-sen-university).

What drug class is Gemcitabine, Vinorelbine, Eribulin, or Utidelone in?

Gemcitabine, Vinorelbine, Eribulin, or Utidelone belongs to the Chemotherapy combination (nucleoside analog, vinca alkaloid, microtubule inhibitor, microtubule stabilizer) class. See all Chemotherapy combination (nucleoside analog, vinca alkaloid, microtubule inhibitor, microtubule stabilizer) drugs at /class/chemotherapy-combination-nucleoside-analog-vinca-alkaloid-microtubule-inhibitor-microtubule-stabilizer.

What development phase is Gemcitabine, Vinorelbine, Eribulin, or Utidelone in?

Gemcitabine, Vinorelbine, Eribulin, or Utidelone is in Phase 3.

What are the side effects of Gemcitabine, Vinorelbine, Eribulin, or Utidelone?

Common side effects of Gemcitabine, Vinorelbine, Eribulin, or Utidelone include Neutropenia, Anemia, Thrombocytopenia, Nausea and vomiting, Peripheral neuropathy, Fatigue.

What does Gemcitabine, Vinorelbine, Eribulin, or Utidelone target?

Gemcitabine, Vinorelbine, Eribulin, or Utidelone targets Multiple: ribonucleotide reductase, microtubules, DNA synthesis and is a Chemotherapy combination (nucleoside analog, vinca alkaloid, microtubule inhibitor, microtubule stabilizer).

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