Agios Pharmaceuticals reported a net income of $947.9 million for Q3 2024, driven by milestone and royalty agreement income. PYRUKYND® net revenue was $9.0 million, and the company's cash, cash equivalents, and marketable securities reached $1.7 billion.
Completed enrollment of the Phase 3 RISE UP study of mitapivat in sickle cell disease, with topline data expected in late 2025.
Received $1.1 billion in payments from Royalty Pharma and Servier following FDA approval of vorasidenib.
Commenced enrollment of the Phase 2b study of tebapivat in lower-risk Myelodysplastic Syndromes (LR-MDS) and was granted FDA Orphan Drug Designation for treatment of MDS.
PYRUKYND® generated $9.0 million in net revenue, a 4% increase from the previous quarter.
Agios anticipates filing an sNDA for mitapivat in thalassemia and presenting additional clinical data at the ASH Congress by the end of 2024.
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