MedCity News April 19, 2024
Frank Vinluan

The FDA expanded the approval of Roche’s Alecensa to include adjuvant treatment of non-small cell lung cancer. The targeted therapy addresses cancers driven by the ALK genetic mutation.

A Roche cancer drug that treats lung cancer with a certain genetic signature now has an additional FDA approval that expands the applications of the blockbuster product.

The drug, Alecensa, is already approved as a first- and second-line treatment for non-small cell lung cancer (NSCLC). The latest approval for the drug permits its use as an adjuvant, a therapy used after the primary cancer treatment (usually surgery) to kill any remaining cancer cells and to reduce the risk of the disease’s return.

Alecensa is a tyrosine kinase inhibitor, a type of drug...

Today's Sponsors

Venturous
Got healthcare questions? Just ask Transcarent

Today's Sponsor

Venturous

 
Topics: Biotechnology, FDA, Govt Agencies, Pharma, Pharma / Biotech
Beam base editing therapy gets ‘proof of concept’ in rare lung disease
Walgreens to go private in $10B deal
The essential biotech news stories of the day
GLP-1s and total joint replacement: 10 things to know
The pharmacy change 'key to your future existence as a health plan'

Share This Article