Allt inom mfn_news

All samples analyzed from the 30 mg dose group in the NEX-22 Phase I study

Nanexa announced today that all pharmacokinetic (PK) samples from the final dose group, 30 mg of the Phase I study for NEX-22, now have been analyzed. The results show increased exposure in line with the dose escalation and further demonstrate a controlled and prolonged release of liraglutide, which supports a one-month depot of liraglutide.

Bulletin from Nanexa’s Annual General Meeting

The Annual General Meeting (AGM) of Nanexa AB (publ) has been held on May 15, 2025, at which meeting submitted proposals were passed. The complete proposals for resolutions are set out in the AGM notice.