Generic Name: pralsetinib

Pronunciation: N/A

Abbreviation: N/A

Other Market Name: N/A

Drug Class: Targeted Therapy Medications

Company: Blueprint/Genentech

Approval Status: Approved

Generic Version Available: No

Experimental Code: BLU-667


Drug Indication

Gavreto is a kinase inhibitor approved for the treatment of metastatic non-small-cell lung cancer with RET gene fusions.


General Info

Gavreto blocks the RET protein, which plays a role in cell proliferation. Mutations and fusions in the RET gene can drive the development of cancer. The ARROW trial showed that Gavreto shrank tumors in 57% of people with previously treated non-small-cell lung cancer with RET fusions and in 70% of those being treated for the first time. Gavreto was first approved in September 2020.


Dosage

Dosing Info:

Gavreto is taken as a capsule once daily on an empty stomach.


Side Effects

The most common adverse reactions include fatigue, constipation, muscle pain, hypertension, elevated ALT liver enzymes and other laboratory abnormalities. Gavreto can cause depletion of red blood cells (anemia), white blood cells (neutropenia) and platelets (thrombocytopenia), which can lead to infections and easy bleeding. Potential serious side effects include lung problems, severe hypertension, liver toxicity, severe bleeding and slow wound healing. Gavreto can cause fetal harm if used during pregnancy.


For More Info: https://www.gene.com/download/pdf/gavreto_patientinfo.pdf

Patient Assistance Program Info: http://www.yourblueprint.com/

Last Reviewed: September 7, 2020