Enregistrement de source primaire
La FDA a approuvé la NDA pour DESMODA (acétate de desmopressine) Solution Orale le 25 février 2026. L'approbation couvre le traitement de substitution antidiurétique pour le diabète insipide central/AVP-D chez les patients de tous âges. Le produit est désormais autorisé pour un lancement commercial aux États-Unis.
eton20260223_8k.htm false 0001710340 0001710340 2026-02-25 2026-02-25 UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 February 25, 2026 Date of Report (Date of earliest event reported) ETON PHARMACEUTICALS, INC. (Exact name of registrant as specified in its charter) Delaware 001-38738 37-1858472 (State of (Commission (I.R.S. Employer incorporation) File Number) Identification Number) 21925 W. Field Parkway, Suite 235 Deer Park , Illinois 60010 -7278 (Address of principal executive offices) (Zip code) ( 847 ) 787-7361 (Registrant ’ s telephone number, including area code) Check the appropriate box below if the Form 8-K filing is intended to simul