FDA Approves ORLADEYO, First Oral HAE Drug for Children
Interim data from APeX-P, the largest pediatric HAE prophylaxis study to date in patients aged 2 to under 12,...
Interim data from APeX-P, the largest pediatric HAE prophylaxis study to date in patients aged 2 to under 12,...
In a Phase 1 expansion of ragistomig, a 4-1BB × PD-L1 bispecific, the 3 mg/kg every-six-weeks regimen delivered an...
Enrollment remains on pace for a Q3 2026 topline readout in Aardvark Therapeutics’ Phase 3 HERO trial of ARD-101...
Samuraciclib plus fulvestrant delivered an overall response rate of 55% and a median progression-free survival of 14.5 months in...
In PD-1 inhibitor–resistant metastatic melanoma, NuCana’s NUC-7738 plus pembrolizumab produced two partial responses (one confirmed) and seven instances of...
In the single-ascending dose portion of the first-in-human AVALON trial (NCT06310291), VTP-1000 was well tolerated with no treatment-related serious...
Accendatech reported that in an exploratory cohort of idiopathic pulmonary fibrosis, 38% of evaluable patients (11 of 29) on...
Post-cycle 6 in newly diagnosed primary CNS lymphoma treated with orelabrutinib, rituximab, and high-dose methotrexate, objective responses reached 89.5%...
Medicenna will unveil updated ABILITY-1 Phase 1/2 data for its long-acting IL-2 superkine MDNA11—both as monotherapy and in combination...
Praxis secured FDA agreement to convert EMBRAVE3, its registrational study of elsunersen in early-onset SCN2A developmental and epileptic encephalopathy,...