Category and country

Therapeutics companies in Norway

7 therapeutics profiles in Norway. Every profile is hand-reviewed with leadership, certifications, and public sources.

Profiles7
Verified7
With certifications2
Cities3
Category view

Where does therapeutics cluster in Norway?

Oslo (5), Orsta (1), and Sandvika (1) Most visible profiles: AlgiPharma AS, Arctic Bioscience AS, Calluna Pharma AS, and Oncoinvent ASA.

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Which standards are already visible?

GMP (2) Latest review: 24 April 2026. Review cycle: April 2026.

Full list

Therapeutics profiles in Norway

7 profiles match the active filter.

Current review cycle

AlgiPharma AS

SandvikaNorwayTherapeutics

Sandvika alginate-chemistry biotech developing OligoG CF-5/20, a low-G alginate oligomer in Phase 2b for cystic fibrosis mucus clearance and biofilm disruption, with EU Horizon 2020 and Cystic Fibrosis Foundation grant support.

Lead
Yngvar P. BergChief Executive Officer
Scale
Clinical-stage alginate oligomer development
0 sources38d reviewPublic-funding disclosures (CFF, Horizon 2020, NRC)Phase 2b cystic-fibrosis program
Current review cycle

Arctic Bioscience AS

OrstaNorwayTherapeutics

Orsta-based marine-lipid pharma and nutraceutical company developing HRO350, a herring-roe-derived Phase IIb candidate for mild-to-moderate psoriasis, alongside the commercial Romega omega-3 phospholipid brand.

Lead
Christer L. ValderhaugChief Executive Officer
Scale
GMP clinical and commercial nutraceutical supply
0 sources38d reviewGMP manufacturing of clinical trial materialOslo Bors listing (ABS.OL)
Current review cycle

Calluna Pharma AS

OsloNorwayTherapeutics

Oslo clinical-stage antibody biotech targeting fibrosis and inflammation through the first-in-class anti-S100A4/S100A9 antibody CAL101, with Phase 1 completed in October 2024 and backing from Forbion.

Lead
Mark GaffneyChief Executive Officer
Scale
Clinical-stage antibody development
0 sources38d reviewPhase 1 completed for CAL101Forbion-backed portfolio company
Current review cycle

Oncoinvent ASA

OsloNorwayTherapeutics

Oslo-listed clinical-stage radiopharmaceutical developer running Phase 2 trials of Radspherin, a radium-224 alpha-emitter microsphere for ovarian peritoneal metastases, following the October 2025 merger with BerGenBio.

Lead
Oystein SougChief Executive Officer
Scale
GMP clinical-trial-material production
0 sources38d reviewGMP manufacturing authorization from the Norwegian Medicines Agency for clinical trial materialFDA Fast Track for Radspherin in ovarian peritoneal metastases
Current review cycle

Thor Medical ASA

OsloNorwayTherapeutics

Oslo-listed radiopharmaceutical developer (formerly Nordic Nanovector) focused on alpha-emitter production (radium-224 and Pb-212) for next-generation cancer therapy, with pilot radionuclide production at Heroya.

Lead
Alf BjorsethChief Executive Officer
Scale
Pilot radiopharmaceutical production
0 sources38d reviewOslo Stock Exchange listing (legacy NANOV now THOR)Pilot radionuclide production at Heroya
Current review cycle

Zelluna ASA

OsloNorwayTherapeutics

Euronext Oslo-listed cell therapy company (formed February 2025 from the Ultimovacs and Zelluna Immunotherapy business combination) developing off-the-shelf TCR-NK cell therapies for solid tumors, with a lead MAGE-A4 program advancing toward IND.

Lead
Namir HassanChief Executive Officer
Scale
Clinical-stage cell therapy development
0 sources38d reviewEuronext Oslo listing (ZLNA, March 2025)Oslo University Hospital Translational Research Unit NK-TCR license
Current review cycle

Nykode Therapeutics

OsloNorwayTherapeutics

Oslo clinical-stage immunotherapy company running its DNA-based platform, oncology programs, and partner-facing operations from the Oslo Science Park headquarters.

Lead
Michael EngsigChief Executive Officer
Scale
Drug Development
Related brief

Read deeper on this category

Regulatory brief

EU Biotech Regulation 2026: What Changed and Who It Affects

A plain reading of the 2026 EU biotech regulatory package — pharmaceutical reform, the European Health Data Space, the AI Act, and the upcoming EU Biotech Act — and what biotech, pharma, and CDMO companies should do about it.

Open brief
FAQ

Frequently asked questions on this category

What does "therapeutics company" mean?
A company that develops drugs to treat or prevent disease, as distinct from contract manufacturers (CDMOs), service organizations (CROs), or tools/diagnostics suppliers. Therapeutic developers own a pipeline of drug candidates and either develop them in-house, license them out, or commercialize them at scale.
Which European countries lead in therapeutics?
Switzerland (Roche, Novartis, Idorsia, Basilea, Noema), Germany (BioNTech, Bayer, Merck KGaA), Denmark (Novo Nordisk, Lundbeck, Genmab, Zealand Pharma), Sweden (AstraZeneca, BioArctic, Sobi), and emerging markets in Poland (Ryvu, Captor), Lithuania (Atrandi, CasZyme), and Estonia (Asper Biogene). The directory covers all of these with hand-reviewed profiles.
How are therapeutics companies verified in this directory?
Every profile is hand-reviewed against an audit framework: leadership identity confirmed by primary source, physical site address sourced from official disclosures, regulatory and pipeline context backed by certification documents or filings, and a registry note explaining the company's current operating focus and clinical stage where applicable.
Can I compare two therapeutic developers side by side?
Yes — use the Compare button on any company card to add it to a comparison set (up to 3 companies), then open the /compare page for a side-by-side view of leadership, certifications, and operating scale.
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