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FDA Approval for Genentech's VENCLEXTA®

On June 8, 2018,  VENCLEXTA® venetoclax tablets) was approved by the US Food and Drug Administration (FDA) for the treatment of patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL), with or without 17p deletion, who have received at least one prior therapy.

 

Genentech BioOncology® Access Solutions is your resource for access and reimbursement support after VENCLEXTA is prescribed. We can help your patients by providing: 

·       Benefits investigations (BIs)

·       Prior authorization (PA) resources

·       Information about authorized specialty pharmacies (SPs) and specialty distributors 

·       Sample billing and coding information

·       Resources for denials and appeals

·       Patient assistance options

A list of authorized specialty pharmacies and specialty distributors is available at                         Genentech-Access.com/VENCLEXTA.

 

For more information about Genentech BioOncology Access Solutions, please visit Genentech-Access.com/VENCLEXTA or call (888) 249-4918.