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• Procedure revenue declined 15.1% to $28.9 million, while dietary supplements revenue grew 7.3% to $12.0 million
• Reported positive Adjusted EBITDA of $44.4 million andNet Incomeof $15.3 million
• Cash, cash equivalents, and marketable securities totaled $528.5 million as of September 30, 2026
• This is the second FDA Orphan Drug Designation for sovleplenib, following its October 2026 designation for primary immune thrombocytopenia (ITP).
• Lacutamab Phase 3 TELLOMAK-3 trial is on track for first patient dosing in Q1 2027, with an FDAAccelerated Approvalfiling planned for H2 2027.
• The ribupatide injection Phase 2b trial and KaiNETIC global Phase 3 program are fully enrolled, with data expected mid-2027 and mid-2028, respectively.
• Ryoncil (remestemcel-L-rknd) was highlighted as a first-line treatment option after steroids for pediatric acute graft-versus-host disease
• 46% of participants on lorundrostat 50 mg achieved the AHA/ACC systolic BP target of less than 130 mmHg at Week 12
• The company expanded its relationship with HealthCareRoyaltythrough a $125 million financing linked to mazdutide royalty payments from Eli Lilly.
•Net Incomerose 11% to $29.5 million, or $0.72 per diluted share, while adjusted EBITDA increased 4% to $64.3 million.
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