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2025-08-28 08:00 Kvartalsrapport 2025-Q2
2025-05-26 N/A Årsstämma
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2024-11-19 - Extra Bolagsstämma 2024
2024-08-29 - Kvartalsrapport 2024-Q2
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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.
2023-01-12 18:21:20

Reference is being made to the stock exchange release from October 10th 2022, where Arctic Bioscience announced that Clinical Trial Application (CTA) for a Phase IIb clinical trial in mild-to-moderate psoriasis with the investigational medicinal product (IMP) HRO350 was submitted to medicinal authorities.

Arctic Bioscience is pleased to announce that the CTA has been approved in the UK. Today, January 12th 2023, the Health Research Authority (HRA) gave its approval for clinical trial start in the UK "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). The CTA was simultaneously also approved by The United Kingdom (UK) Medicines & Healthcare products Regulatory Agency (MHRA), the UK Research Ethics Committee (REC). This is a major regulatory milestone in the drug development program for HRO350.

Arctic Bioscience is currently in the process of activating the clinical trial sites in the UK, and first patient inclusion is expected later this month.

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