More Kringle Pharma, Inc. news
Kringle Pharma, Inc.TSE: 4884

Kringle Pharma Receives FDA Clearance of IND Application for Oremepermin Alfa in Acute Spinal Cord Injury

Oct 18, 2026 at 9:45 PM EDT · Issued by Kringle Pharma, Inc. via TDnet

Filed with TSE · Oct 18, 2026 at 9:45 PM EDT · 2 pages · English

On 6ix: 6ix.com/news/kringle-pharma-receives-fda-clearance-of-ind-application-for-oremepermin-alfa-in-acute-spinal-cord-injury

Kringle Pharma, Inc. on 6ix

Story so far

  • Kringle Pharma Announces IND Submission to the U.S. FDA for Oremepermin Alfa for the Treatment of Acute Spinal Cord InjurySep 24, 2026
  • Kringle Pharma Advances the Registrational Program for Oremepermin Alfa in Japan with Initiation of Additional Phase 3 in Acute Spinal Cord InjuryJul 24, 2026

Earlier from Kringle Pharma

  • Kringle Pharma Announces IND Submission to the U.S. FDA for Oremepermin Alfa for the Treatment of Acute Spinal Cord InjurySep 24
  • Financial Results for the Nine Months Ended June 30, 2026 [Japanese GAAP] (Non-consolidated)Aug 10
  • Kringle Pharma Advances the Registrational Program for Oremepermin Alfa in Japan with Initiation of Additional Phase 3 in Acute Spinal Cord InjuryJul 23
  • Update on the Investigator-initiated Phase 2 Study in Patients with ALSAug 12, 2022
  • Kringle Pharma Files Patent Application for Treatment of Chronic Spinal Cord InjuryMar 11, 2022
All Kringle Pharma news releases↗

Follow Kringle Pharma into a list and get an email when it puts out news.

Follow Kringle Pharma
  • About 6ix
  • Editorial & Sourcing
  • Corrections
  • Contact
  • Privacy
  • Terms
  • Disclaimer