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Gemcitabine and Erlotinib

Grupo Espanol Multidisciplinario del Cancer Digestivo · Phase 2 active Small molecule

Gemcitabine is a nucleoside analog that inhibits DNA synthesis, while Erlotinib is a tyrosine kinase inhibitor that targets the epidermal growth factor receptor (EGFR).

Gemcitabine is a nucleoside analog that inhibits DNA synthesis, while Erlotinib is a tyrosine kinase inhibitor that targets the epidermal growth factor receptor (EGFR). Used for Pancreatic cancer, Non-small cell lung cancer.

At a glance

Generic nameGemcitabine and Erlotinib
Also known asGemcitabine and Tarceva
SponsorGrupo Espanol Multidisciplinario del Cancer Digestivo
Drug classNucleoside analog and tyrosine kinase inhibitor
TargetDNA and EGFR
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 2

Mechanism of action

Gemcitabine works by incorporating itself into DNA, causing DNA damage and inhibiting cancer cell growth. Erlotinib, on the other hand, binds to the EGFR, preventing the receptor from activating downstream signaling pathways that promote cell proliferation and survival.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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