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The Cancer Letter
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Drugs & Targets

FDA approves Pluvicto for metastatic castration-resistant prostate cancer

March 25, 2022
Vol.48 No.12
Drugs & Targets

FDA approves Opdivo and platinum-doublet chemotherapy for early-stage NSCLC

March 11, 2022
Vol.48 No.10
Drugs & Targets

FDA grants priority review to Tibsovo in combination with azacitidine in previously untreated IDH1-mutated AML

March 11, 2022
Vol.48 No.10
Drugs & Targets

FDA clinical trial guidances touch on Biden administration’s goals for advancing development of cancer treatments

March 11, 2022
Vol.48 No.10
Drugs & Targets

Six months after court-ordered deadline, FDA hasn’t ruled on major e-cigarette manufacturers’ product applications, advocates say

March 11, 2022
Vol.48 No.10
In Brief

Robert Califf confirmed as FDA commissioner

February 18, 2022
Vol.48 No.07
Drugs & Targets

FDA grants Fast Track designation to IO-202, anti-LILRB4 myeloid checkpoint inhibitor for AML

February 18, 2022
Vol.48 No.07
In a 14:1 vote, ODAC nixes a PD-1 drug developed in China; data not generalizable to U.S. population
Regulatory News

In a 14:1 vote, ODAC nixes a PD-1 drug developed in China; data not generalizable to U.S. population

February 11, 2022
Vol.48 No.06
By Paul Goldberg and Alice Tracey
FDA says it had no input as companies developed checkpoint inhibitors in China
Conversation with The Cancer LetterRegulatory News

FDA says it had no input as companies developed checkpoint inhibitors in China

February 04, 2022
Vol.48 No.05
By Paul Goldberg
Drugs & Targets

FDA investigating possible increased risk of death with lymphoma drug Ukoniq

February 04, 2022
Vol.48 No.05

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