Fredag 18 September | 09:49:54 Europe / Stockholm
Est. tid*
2027-03-03 N/A Bokslutskommuniké 2026
2026-08-20 - Kvartalsrapport 2026-Q2
2026-04-07 - X-dag ordinarie utdelning GUBRA 0.00 DKK
2026-03-26 - Årsstämma
2026-02-27 - Bokslutskommuniké 2025
2025-08-21 - Kvartalsrapport 2025-Q2
2025-06-30 - X-dag bonusutdelning GUBRA 61.2
2025-06-27 - Extra Bolagsstämma 2025
2025-04-04 - X-dag ordinarie utdelning GUBRA 0.00 DKK
2025-04-03 - Årsstämma
2025-02-28 - Bokslutskommuniké 2024
2024-08-23 - Kvartalsrapport 2024-Q2
2024-04-04 - X-dag ordinarie utdelning GUBRA 0.00 DKK
2024-04-03 - Årsstämma
2024-02-28 - Bokslutskommuniké 2023
2023-11-01 - Extra Bolagsstämma 2023
2023-08-25 - Kvartalsrapport 2023-Q2
LandDanmark
ListaMid Cap Copenhagen
SektorHälsovård
IndustriBioteknik
Gubra är ett läkemedelsbolag. Bolagets verksamhet är fokuserad på de tidiga stadierna av läkemedelsutveckling. De driver huvudsakligen forskning och utveckling inom området för metabola och fibrotiska sjukdomar. Bolagets produktportfölj innefattar ett flertal varumärken och läkemedel, och verksamheten bedrivs på global nivå, med störst närvaro inom Nordamerika och Norden. Huvudkontoret ligger i Hørsholm, Danmark.

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Gubra collaboration partner Hemab announces first participant dosed in Phase 1 clinical trial of HMB-003, an investigational therapy for the management of heavy menstrual bleeding

2026-09-17 14:45:00

Today, Gubra announced that its partner Hemab Therapeutics has dosed the first healthy volunteer in its Phase 1 clinical trial evaluating HMB-003, an investigational therapy for the management of heavy menstrual bleeding. HMB-003 was discovered under a collaboration between Gubra and Hemab Therapeutics, combining Gubra’s streaMLine™ peptide discovery platform with Hemab’s expertise in bleeding disorders. HMB-003 is proprietary to Hemab, and Hemab is solely responsible for its development and commercialization.

The Phase 1 study (NCT07798505) is a randomized, placebo-controlled, single-ascending-dose escalation trial designed to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of HMB-003 in healthy adult volunteers.

Further details are available in Hemab Therapeutics’ press release: https://ir.hemab.com/news-releases/news-release-details/hemab-therapeutics-announces-first-participant-dosed-phase-1

About HMB-003
HMB-003 is a subcutaneously administered peptide-based plasmin inhibitor with a durable half-life - a proven therapeutic target in coagulation medicine - being developed as a novel antifibrinolytic designed to reduce bleeding across multiple settings. Engineered to directly inhibit plasmin at its active site, HMB-003 blocks fibrinolysis independently of the plasminogen activation pathway. HMB-003 is optimized to provide sustained bleed protection across multiple high-unmet-need conditions, ranging from heavy menstrual bleeding and hereditary hemorrhagic telangiectasia to peri-operative bleeding management. For more information, please visit clinicaltrials.gov (NCT07798505).

In 2023, Gubra and Hemab Therapeutics entered into a collaboration agreement to discover a novel peptide drug candidate. The project combines Gubra’s streaMLineTM peptide discovery platform with Hemab’s expertise in in bleeding disorders. HMB-003 was discovered under this collaboration agreement. Hemab is solely responsible for development and commercialization of HMB-003.