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The Cancer Letter
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Drugs & Targets

FDA approves Opdivo + cisplatin + gemcitabine for unresectable or metastatic urothelial carcinoma

March 08, 2024
Vol.50 No.10
Drugs & Targets

FDA grants accelerated approval to Brukinsa for R/R follicular lymphoma

March 08, 2024
Vol.50 No.10
Drugs & Targets

FDA approves for first denosumab biosimilars

March 08, 2024
Vol.50 No.10
Drugs & Targets

Elipses’s selective RET inhibitor EP0031/A400 granted Fast Track designation in NSCLC

March 08, 2024
Vol.50 No.10
Drugs & Targets

FDA issues final decision to withdraw approval of Pepaxto

March 01, 2024
Vol.50 No.09
Drugs & Targets

FDA, industry actions end sales of PFAS in U.S. food packaging

March 01, 2024
Vol.50 No.09
Drugs & Targets

FDA grants Epkinly priority review sBLA for difficult-to-treat R/R follicular lymphoma

March 01, 2024
Vol.50 No.09
Drugs & Targets

FDA accepts BLA for Tevimbra for 1L treatment of G/GEJ cancers

March 01, 2024
Vol.50 No.09
First-ever commercial TIL therapy: How NCI, Iovance, and Moffitt achieved FDA approval

First-ever commercial TIL therapy: How NCI, Iovance, and Moffitt achieved FDA approval

February 23, 2024
Vol.50 No.08
By Matthew Bin Han Ong
Steven Rosenberg, Friedrich Graf Finckenstein: FDA recognition of TIL therapy is the result of 40 years of research
Conversation with The Cancer Letter

Steven Rosenberg, Friedrich Graf Finckenstein: FDA recognition of TIL therapy is the result of 40 years of research

February 23, 2024
Vol.50 No.08
By Matthew Bin Han Ong

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