Drug intelligence / Profile preview

trilaciclib + docetaxel

Development stage
Unknown
Lead developer
G1 Therapeutics
Modality
Small Molecules
Administration
Intravenous
01

Overview

**Trilaciclib + docetaxel** is an investigational combination therapy currently being evaluated in clinical trials for patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) who have failed at least one prior line of therapy. Trilaciclib is a cyclin-dependent kinase 4/6 (CDK4/6) inhibitor administered intravenously before docetaxel chemotherapy. Its primary purpose in this combination is to protect bone marrow from chemotherapy-induced myelosuppression by transiently arresting hematopoietic stem and progenitor cells in the G1 phase, thereby reducing the incidence and severity of toxicities like neutropenia and febrile neutropenia. Docetaxel is a taxane-class chemotherapeutic agent that inhibits microtubule depolymerization, leading to cell cycle arrest and apoptosis in rapidly dividing cancer cells. The combination is being investigated in phase II studies for its efficacy in reducing hematologic toxicity and improving outcomes in NSCLC[1][3][5].

Brand names
CoselaTaxotere
Other names
trilaciclib + docetaxel
02

Targets

SLC47A1 (Multidrug and toxin extrusion transporter 1)CDK6 (Cyclin-dependent kinase 6)OCT2 (Organic cation transporter 2)CDK4 (Cyclin-dependent kinase 4)MATE2-K (Multidrug and toxin extrusion protein 2)TUBB (Tubulin (alpha and beta subunits))

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