FDA Approval Sought for Rituximab Biosimilar
A biologics license application has been submitted to the FDA for the rituximab biosimilar ABP 798.
A biologics license application has been submitted to the FDA for the rituximab biosimilar ABP 798.
Emil Lou, MD, PhD, FACP, discusses the potential applicability of CRISPR-Cas9–mediated CISH knockout to bolster TIL responses in drug-refractory GI tumors.
R . Lor Randall, MD, FACS, discusses disparities in global access to care for patients with sarcoma.
Relacorilant plus nab-paclitaxel improved survival in platinum-resistant ovarian cancer with a primary platinum-free interval of 1 to 6 months.
Martin E. Gutierrez, MD, discusses steps towards a continuous shift in both the NSCLC and SCLC treatment paradigms, based on trials presented at ASCO 2025.
Adjuvant dalpiciclib plus endocrine therapy met the iDFS primary end point in the DAWNA-A trial in HR-positive, HER2-negative early breast cancer.
Darren Pan, MD, discusses updates regarding cilta-cel and anito-cel for the treatment of patients with relapsed/refractory multiple myeloma.
Safety and efficacy data for elotuzumab support its further investigation in the treatment of myelofibrosis.
Qian (Janie) Qin, MD, discusses the current arsenal of radioligand therapies in metastatic castration-resistant prostate cancer.
High doses of corticosteroids are likely the most significant factor in why some immunotherapies don’t work.
In an OncLive Peer Exchange filmed during EBMT, investigators discuss approaches to optimizing allo-HSCT and preventing GVHD in hematologic malignancies.