FDA Approves Venetoclax for CLL

Apr 10

2016

The U. S. Food and Drug Administration approved venetoclax (VENCLEXTA tablets, marketed by AbbVie, Inc. and Genentech USA, Inc.) for the treatment of patients with chronic lymphocytic leukemia (CLL) with 17p deletion, as detected by an FDA-approved test, who have received at least one prior therapy.

Citations

APA

American Society of Hematology. (2016).
FDA Approves Venetoclax for CLL.
Retrieved from https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2016/fda-approves-venetoclax-for-cll.

Chicago

American Society of Hematology.
"FDA Approves Venetoclax for CLL." Hematology.org.
https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2016/fda-approves-venetoclax-for-cll
(label-accessed December 11, 2024).

MLA

"American Society of Hematology."
FDA Approves Venetoclax for CLL, 11 Dec. 2024 ,
https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2016/fda-approves-venetoclax-for-cll.

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