FDA Issues Guidance Considerations for Tissue Biopsies in Clinical Trials
According to the FDA, biopsies should be optional in clinical protocol when information will be used to evaluate only non-key secondary end points.
According to the FDA, biopsies should be optional in clinical protocol when information will be used to evaluate only non-key secondary end points.
The FDA has granted priority review to the NDA seeking the approval for taletrectinib in ROS1-positive advanced non–small cell lung cancer.
Akriti Jain, MD, discusses her presentation from the 2024 American Society of Hematology Meeting and Exposition.
CheckMate 73L missed its primary end point of PFS in advanced unresectable stage III non–small cell lung cancer.
Speakers at the 2024 American Urological Association (AUA) annual meeting highlighted the innovations and advancements that are pushing the field of urology forward.
An abstract is unavailable.
THE LINK BETWEEN ALCOHOL CONSUMPTION AND CANCER
New drug hope for prostate cancer patients
China’s NMPA has approved taletrectinib for locally advanced or metastatic ROS1-positive non–small cell lung cancer after a previous ROS1 TKI.
Zongertinib demonstrated clinically meaningful efficacy in previously treated HER2-mutated non–small cell lung cancer.