AI-powered trial screening helps community oncology practices identify eligible patients locally, widening access beyond ...
Zanidatamab plus tislelizumab and chemotherapy reduced mortality risk by 28% versus trastuzumab plus chemotherapy, delivering ...
The first patient has been dosed in MODeFIRe-1 (NCT07745361), a phase 2 study evaluating MRT-2359 in combination with ...
The recent FDA approval of iberdomide (Zenbexus) represents more than the approval of a single new drug for ...
The benefit of daraxonrasib in PDAC may be overstated in RASolute 302 due to informative censoring. The RASolute 302 trial (NCT06625320) in pancreatic cancer has received a lot of attention. The study ...
Priority review reflects AZUR-1 meeting its primary end point of meaningful, sustained 12-month cCR in dMMR/MSI-H stage ...
Sustained MRD negativity at 12 months was higher with D-VRd, with similar advantages at 24 and 36 months and a lower rate of ...
Primary endpoint results showed no SSE-FS benefit with radium-223 addition (HR 1.46; 1-sided P=.12), while OS, PFS, and ORR ...
As artificial intelligence (AI) becomes more integrated into clinical trial matching, human oversight remains an important ...
Laila Alkhouli, MD, of Cleveland Children's Clinic outlines critical findings from research evaluating how care teams across ...
Hearn Jay Cho, MD, explains how immune profiling could inform what impairs T-cell fitness, a crucial consideration when using CAR T-cell therapy or bispecific T-cell engagers. Hearn Jay Cho, MD, PhD, ...
The FDA has granted fast track designation to safusidenib, an oral IDH1 inhibitor, based on durable phase 2 J201 study ...
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