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The Cancer Letter
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Drugs & Targets

FDA approves Retevmo for medullary thyroid cancer with RET mutation

October 04, 2024
Vol.50 No.37
Drugs & Targets

FDA approves Cologuard Plus Test for non-invasive CRC screening

October 04, 2024
Vol.50 No.37
Drugs & Targets

FDA approves Sarclisa + VRd for MM not eligible for transplant

September 27, 2024
Vol.50 No.36
Drugs & Targets

FDA approves Tagrisso for stage 3 EGFR-mutated NSCLC

September 27, 2024
Vol.50 No.36
Drugs & Targets

Bayer submits sNDA to FDA for expanded indication for Nubeqa for treatment of mHSPC

September 27, 2024
Vol.50 No.36
Melanoma investigators invite FDA to publicly discuss approval endpoints and crossover design
Regulatory News

Melanoma investigators invite FDA to publicly discuss approval endpoints and crossover design
The agency accepts the invitation

September 20, 2024
Vol.50 No.35
By Paul Goldberg
Drugs & Targets

FDA approves Keytruda + pemetrexed + chemo in first-line mesothelioma indication

September 20, 2024
Vol.50 No.35
Drugs & Targets

FDA approves Rybrevant + pemetrexed + chemo in NSCLC with EGFR exon 19 deletions or L858R mutations

September 20, 2024
Vol.50 No.35
Drugs & Targets

FDA approves Kisqali + aromatase inhibitor for early high-risk breast cancer

September 20, 2024
Vol.50 No.35
Drugs & Targets

FDA grants Fast Track designation for ICT01 + Azacitidine + Venetoclax in treatment of first-line AML unfit for induction chemo

September 20, 2024
Vol.50 No.35

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