Abstract B163: First-in-patient study of PF-04691502, a small molecule intravenous dual inhibitor of PI3K and mTOR in patients with advanced cancer: Update on safety, efficacy, and pharmacology.

Author(s):  
Robert Millham ◽  
Brett Houk ◽  
Gary Borzillo ◽  
Patricia LoRusso ◽  
Lisa Marburg ◽  
...  
2014 ◽  
Vol 32 (3) ◽  
pp. 510-517 ◽  
Author(s):  
Carolyn D. Britten ◽  
Alex A. Adjei ◽  
Robert Millham ◽  
Brett E. Houk ◽  
Gary Borzillo ◽  
...  

2015 ◽  
Vol 21 (8) ◽  
pp. 1888-1895 ◽  
Author(s):  
Geoffrey I. Shapiro ◽  
Katherine M. Bell-McGuinn ◽  
Julian R. Molina ◽  
Johanna Bendell ◽  
James Spicer ◽  
...  

2014 ◽  
Vol 32 (3) ◽  
pp. 575-575
Author(s):  
Carolyn D. Britten ◽  
Alex A. Adjei ◽  
Robert Millham ◽  
Brett E. Houk ◽  
Gary Borzillo ◽  
...  

2006 ◽  
Vol 4 (7) ◽  
pp. 1502-1509 ◽  
Author(s):  
E. U. GRAEFE-MODY ◽  
U. SCHUHLY ◽  
K. RATHGEN ◽  
H. STAHLE ◽  
J. M. LEITNER ◽  
...  

Author(s):  
Vollmer David ◽  
Jared Bearss ◽  
Carissa Jones ◽  
Virgil McCarthy ◽  
Eric Gourley ◽  
...  

2019 ◽  
Vol 12 (2) ◽  
pp. 69 ◽  
Author(s):  
Daniel A. Rodrigues ◽  
Fernanda S. Sagrillo ◽  
Carlos A. M. Fraga

Duvelisib (Copiktra®) is a dual inhibitor of phosphoinositide 3-kinases (PI3Kδ and PI3Kγ). In 2018, duvelisib was first approved by the Food and Drug Administration (FDA) for the treatment of adult patients with relapsed or refractory chronic lymphocytic leukaemia (CLL)/ small lymphocytic lymphoma (SLL) after at least two prior therapies. Duvelisib has also been approved under accelerated track for relapsed or refractory follicular lymphoma (FL) after at least two prior systemic therapies. In this review, we provide a series of information about duvelisib, such as the development of clinical trials for LLC/SLL and FL and the steps used for its synthesis.


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