FDA Accepts NDA for Avatrombopag in Pediatric Thrombocytopenia
Results from the phase 3 AVA-PED-301 trial support the FDA decision for avatrombopag in pediatric thrombocytopenia.
Results from the phase 3 AVA-PED-301 trial support the FDA decision for avatrombopag in pediatric thrombocytopenia.
AACR is hosting a workshop with the FDA on January 16, 2025, to discuss the considerations for routine testing of DPD deficiency before treatment with…
Melissa Calopiz, University of Michigan, Ann Arbor, MI, explores the use of SimADC, a computational model for designing and evaluating antibody-drug conjugates (ADCs). By simulating…
India is witnessing a surge in global pharmaceutical companies establishing and expanding their presence, with Hyderabad emerging as a key…
Presentations at the 2024 San Antonio Breast Cancer Symposium examined ways to predict responses to treatments for HR+ HER2- breast cancer.
Publishes monographs dealing with cancer and closely related research fields, or related groups of papers on specific subjects of importance to cancer research.
Is this donation tax deductible? Society Of Surgical Oncology Inc is a 501(c)3 tax-exempt organization and your donation is tax-deductible within the guidelines of U.S.…
Updated results from the 1b/2 ELEVATE study elucidate synergizing effects observed with elacestrant plus targeted therapies in ER+/HER2– breast cancer.
Dr Herrera explains why N+AVD is a strong candidate for primary treatment in adolescent and adult patients with stage III or IV Hodgkin lymphoma.
AbstractBackground. Patients with a germline BRCA pathogenic variant (gBRCA-PV) and advanced high grade ovarian carcinoma (aHGOC) experience higher hematol