TLX101-CDx Given Complete Response Letter for Glioma Imaging
The FDA granted a complete response letter with no safety concerns for the new drug application for TLX101-CDx’s use in glioma imaging.
The FDA granted a complete response letter with no safety concerns for the new drug application for TLX101-CDx’s use in glioma imaging.
An update to the NCCN guidelines recommends naxtiamab-gqgk for adult and pediatric patients with high-risk neuroblastoma.
The FDA has granted accelerated approval to avutometinib and defactinib in KRAS-mutated recurrent low-grade serious ovarian cancer.
Black and Hispanic pediatric patients with high-risk neuroblastoma had significantly lower 5-year survival rates in induction and/or consolidation trials.
A registered nurse gives best practices for use of subcutaneous daratumumab in multiple myeloma.
New data show strong overall survival rates, building on previously reported outcomes with efti plus pembrolizumab for head and neck squamous cell carcinoma.
Early-phase LUPER trial results suggest the lurbinectedin/pembrolizumab combination may benefit patients with relapsed small cell lung cancer.
Clinical trials can provide patients with myeloproliferative neoplasms expanded treatment options.
Final data from the phase 3 ALCYONE trial support frontline use of daratumumab-based therapy for patients with transplant-ineligible newly diagnosed multiple myeloma.
Approvals in oncology during April included treatments for breast cancer, colorectal cancer, and more.
Cretostimogene grenadenorepvec showed complete response across subgroups in patients with high-risk BCG-unresponsive non-muscle invasive bladder cancer.