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The Cancer Letter
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Drugs & Targets

FDA publishes final guidance on drug development for AML

October 21, 2022
Vol.48 No.38
Drugs & Targets

FDA publishes draft guidance on characterizing, collecting, and reporting immune-mediated adverse reactions

October 21, 2022
Vol.48 No.38
Drugs & Targets

FDA publishes draft guidance on tissue agnostic drug development in oncology

October 21, 2022
Vol.48 No.38
Clinical Roundup

New data show more than 2.5M U.S. youth use e-cigarettes

October 07, 2022
Vol.48 No.36
Drugs & Targets

FDA grants accelerated approval to Lytgobi for cholangiocarcinoma

October 07, 2022
Vol.48 No.36
ODAC nixes three cancer drug indications, citing dose uncertainty

ODAC nixes three cancer drug indications, citing dose uncertainty

September 30, 2022
Vol.48 No.35
By Jacquelyn Cobb
FDA spells out new systematic approach to giving out–and taking away–accelerated approvals in oncology
Conversation with The Cancer Letter

FDA spells out new systematic approach to giving out–and taking away–accelerated approvals in oncology

September 23, 2022
Vol.48 No.34
By Paul Goldberg
Drugs & Targets

FDA approves Retevmo for locally advanced or metastatic RET fusion-positive solid tumors, NSCLC

September 23, 2022
Vol.48 No.34
Drugs & Targets

FDA approves Pedmark to reduce the risk of ototoxicity associated with cisplatin for localized pediatric solid tumors

September 23, 2022
Vol.48 No.34
Drugs & Targets

FDA issues safety alert for squamous cell carcinoma and various lymphomas in scar tissue around breast implants

September 16, 2022
Vol.48 No.33

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