Kringle Pharma Receives FDA Clearance of IND Application for Oremepermin Alfa in Acute Spinal Cord Injury10/19 10:45TDnetPDF(151KB)
Kringle Pharma Announces IND Submission to the U.S. FDA for Oremepermin Alfa for the Treatment of Acute Spinal Cord Injury9/24 9:00TDnetPDF(150KB)
Financial Results for the Nine Months Ended June 30, 2026 [Japanese GAAP] (Non-consolidated)8/10 15:40TDnetPDF(296KB)
Kringle Pharma Advances the Registrational Program for Oremepermin Alfa in Japan with Initiation of Additional Phase 3 in Acute Spinal Cord Injury7/24 11:30TDnetPDF(151KB)