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Gemcitabine with R115777

Johnson & Johnson Pharmaceutical Research & Development, L.L.C. · Phase 3 active Small molecule

Gemcitabine with R115777 is a Nucleoside analog + farnesyltransferase inhibitor combination Small molecule drug developed by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.. It is currently in Phase 3 development for Pancreatic cancer, Advanced solid tumors.

Gemcitabine is a nucleoside analog that inhibits DNA synthesis, while R115777 is a farnesyltransferase inhibitor that blocks Ras protein activation, together targeting cancer cell proliferation through complementary pathways.

Gemcitabine is a nucleoside analog that inhibits DNA synthesis, while R115777 is a farnesyltransferase inhibitor that blocks Ras protein activation, together targeting cancer cell proliferation through complementary pathways. Used for Pancreatic cancer, Advanced solid tumors.

At a glance

Generic nameGemcitabine with R115777
SponsorJohnson & Johnson Pharmaceutical Research & Development, L.L.C.
Drug classNucleoside analog + farnesyltransferase inhibitor combination
TargetRibonucleotide reductase (gemcitabine); farnesyltransferase (R115777)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Gemcitabine acts as a deoxycytidine analog that is incorporated into DNA, causing chain termination and inhibiting ribonucleotide reductase to deplete deoxyribonucleotides. R115777 inhibits farnesyltransferase, preventing the post-translational modification and membrane localization of Ras proteins, which are frequently mutated in pancreatic and other cancers. The combination targets both DNA synthesis and oncogenic signaling pathways.

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

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Frequently asked questions about Gemcitabine with R115777

What is Gemcitabine with R115777?

Gemcitabine with R115777 is a Nucleoside analog + farnesyltransferase inhibitor combination drug developed by Johnson & Johnson Pharmaceutical Research & Development, L.L.C., indicated for Pancreatic cancer, Advanced solid tumors.

How does Gemcitabine with R115777 work?

Gemcitabine is a nucleoside analog that inhibits DNA synthesis, while R115777 is a farnesyltransferase inhibitor that blocks Ras protein activation, together targeting cancer cell proliferation through complementary pathways.

What is Gemcitabine with R115777 used for?

Gemcitabine with R115777 is indicated for Pancreatic cancer, Advanced solid tumors.

Who makes Gemcitabine with R115777?

Gemcitabine with R115777 is developed by Johnson & Johnson Pharmaceutical Research & Development, L.L.C. (see full Johnson & Johnson Pharmaceutical Research & Development, L.L.C. pipeline at /company/johnson-johnson-pharmaceutical-research-development-l-l-c).

What drug class is Gemcitabine with R115777 in?

Gemcitabine with R115777 belongs to the Nucleoside analog + farnesyltransferase inhibitor combination class. See all Nucleoside analog + farnesyltransferase inhibitor combination drugs at /class/nucleoside-analog-farnesyltransferase-inhibitor-combination.

What development phase is Gemcitabine with R115777 in?

Gemcitabine with R115777 is in Phase 3.

What are the side effects of Gemcitabine with R115777?

Common side effects of Gemcitabine with R115777 include Myelosuppression (neutropenia, thrombocytopenia), Nausea and vomiting, Fatigue, Diarrhea, Elevated liver enzymes.

What does Gemcitabine with R115777 target?

Gemcitabine with R115777 targets Ribonucleotide reductase (gemcitabine); farnesyltransferase (R115777) and is a Nucleoside analog + farnesyltransferase inhibitor combination.

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