บันทึกจากแหล่งปฐมภูมิ
The company reiterated its plan to submit the NDA for ALXN1840 (tiomolibdate choline) to the FDA in mid-2026. New Phase 3 FoCus trial neurologic and liver-disease data were presented at AAN 2026 and will be shown at EAN and EASL 2026, but no regulatory filing has yet occurred.
EX-99.1 2 ex_962976.htm EXHIBIT 99.1 ex_962976.htm Exhibit 99.1 Monopar Therapeutics Reports First Quarter 2026 Financial Results and Provides Business Updates Wilmette, IL, May 14, 2026 – Monopar Therapeutics Inc. (“Monopar” or the “Company”) (Nasdaq: MNPR), a clinical‐stage biopharmaceutical company developing innovative treatments for patients with unmet medical needs, today announced first quarter 2026 financial results and provided business updates. Recent Program Developments ALXN1840 for Wilson Disease – NDA Submission on Track for Mid-2026 In April 2026, Monopar presented new analyses from the randomized controlled Phase 3 FoCus trial of ALXN1840 (tiomolibdate choline, TMC) at the American Academy of Neurology (AAN) Annual Meeting 2026. The late-breaker oral and poster pres
Monopar จะนำเสนอการวิเคราะห์การทดลอง ALXN1840 FoCus ที่งาน EAN 2026
Monopar: ข้อมูลประโยชน์ทางระบบประสาทของ ALXN1840 ที่งาน EAN 2026
Monopar นำเสนอข้อมูลทางระบบประสาทของ ALXN1840 ในการประชุม AAN 2026