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Kalender

Est. tid*
2025-08-28 08:00 Kvartalsrapport 2025-Q2
2025-05-27 N/A X-dag ordinarie utdelning ABS 0.00 NOK
2025-05-26 N/A Årsstämma
2025-05-07 - Bokslutskommuniké 2024
2024-11-19 - Extra Bolagsstämma 2024
2024-08-29 - Kvartalsrapport 2024-Q2
2024-04-29 - X-dag ordinarie utdelning ABS 0.00 NOK
2024-04-26 - Årsstämma
2024-04-09 - Bokslutskommuniké 2023
2023-09-29 - Kvartalsrapport 2023-Q2
2023-04-24 - X-dag ordinarie utdelning ABS 0.00 NOK
2023-04-21 - Årsstämma
2023-03-29 - Bokslutskommuniké 2022
2022-08-25 - Kvartalsrapport 2022-Q2
2022-05-06 - X-dag ordinarie utdelning ABS 0.00 NOK
2022-05-05 - Årsstämma
2022-04-07 - Bokslutskommuniké 2021
2021-11-10 - Extra Bolagsstämma 2021
2021-08-26 - Kvartalsrapport 2021-Q2

Beskrivning

LandNorge
ListaEuronext Growth Oslo
SektorHälsovård
IndustriBioteknik
Arctic Bioscience är ett bioteknikföretag som utvecklar och kommersialiserar läkemedelsprodukter och kosttillskott baserade på bioaktiva marina råvaror. Företaget utvecklar HRO350, en ny läkemedelskandidat för behandling av patienter med mild till måttlig psoriasis. Kosttillskott säljs globalt både som bulkingredienser och som färdiga produkter under varumärket ROMEGA, till både företag och privatkunder.
2023-03-07 10:36:50

Reference is being made to the stock exchange release from January 12[th], 2023, where Arctic Bioscience announced that the Clinical Trial Application (CTA) for a phase IIb clinical trial in mild-to-moderate psoriasis with the investigational medicinal product HRO350 was approved in the United Kingdom (UK). Arctic Bioscience is pleased to announce that the CTA also has been approved in Norway, Finland, Germany and Poland.

As announced on January 31[st], 2023, Arctic Bioscience met a key milestone when the first patient was included in the clinical trial "A phase IIb, multicenter, randomized, double-blind, placebo-controlled, dose-finding, efficacy and safety study of HRO350 in patients with mild-to-moderate psoriasis" (the `HeROPA' study) in the UK. The study is now also approved in the EU/EEA. With these approvals, we have achieved inclusion of all five countries we had intended for in the study. Sites in the EU/EEA countries participating in the trial will be activated and recruitment of patients can start in these countries.

The large, international HeROPA study will include 519 patients in these five countries. A six-month inclusion period is expected, with first data readout six months after last patient is enrolled.

This information is subject to the disclosure requirements pursuant to section 5-12 of the Norwegian Securities Act.