• Center on Health Equity & Access
  • Clinical
  • Health Care Cost
  • Health Care Delivery
  • Insurance
  • Policy
  • Technology
  • Value-Based Care

Gavreto, FDA Approved for Treatment of Metastatic RET Fusion-Positive NSCLC, Available at Biologics by McKesson

Article

Gavreto was granted accelerated approval by the FDA on September 4, 2020, for the treatment of adult patients with metastatic RET fusion-positive non–small cell lung cancer (NSCLC).

CARY, N.C.Biologics by McKesson, an independent specialty pharmacy specializing in oncology and rare disease areas, has been selected by Blueprint Medicines as a specialty pharmacy provider for Gavreto (pralsetinib) for the treatment of adult patients with metastatic RET fusion-positive non–small cell lung cancer (NSCLC) as detected by an FDA-approved test.

Gavreto, which was granted accelerated approval by the FDA on September 4, 2020, was specifically designed to inhibit RET alterations. RET fusions are oncogenic drivers for multiple solid tumor types. This drug was given priority review by the FDA, which is granted to drugs that are expected to have a large impact on a disease’s treatment.

“Gavreto gives patients a new RET inhibitor option for treating their RET-driven metastatic NSCLC,” said Allison Kinnarney, director of Clinical Programs with Biologics.


Learn more.

Related Videos
Frederick L Locke, MD, Moffitt
Sam Peasah, PhD, MBA, RPh, director for the Center of High-Value Health Care at the University of Pittsburgh Medical Center (UPMC)
Erin Weber, MS
Cathy Eng, MD, FACP, FASCO, Vanderbilt-Ingram Cancer Center
Sam Peasah, PhD, MBA, RPh, director for the Center of High-Value Health Care at the University of Pittsburgh Medical Center (UPMC)
Erin Weber, MS
Andrew Kuykendall, MD
AMCP Recap 2025
Andrew Evens, DO
Screenshot from interview with Andrew Evens, DO
Related Content
© 2025 MJH Life Sciences
AJMC®
All rights reserved.