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No 04 2024

Malin Otmani

-

November 28, 2024

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Updated: January 31, 2025, 09:21 am

Published: November 28, 2024

Top stories

Financing – May 22, 2026

Neobiomics receives investment from HealthCap

The company has announced an investment led by HealthCap, and conjunction with this capital infusion, Neobiomics strengthens its board with the appointment of a new director, Mårten Steen, Managing Partner at HealthCap. 

Collaboration – May 20, 2026

Western Sweden unites to boost life sciences competitiveness

Industry, academic, and public stakeholders will join forces in a new council aimed at accelerating the region’s life science development.

Clinical Trials – May 20, 2026

Oncopeptides secures regulatory approval to start Window-of-Opportunity study

Oncopeptides’ clinical trial application for the “Window-of-Opportunity” (WoO) study in glioblastoma has been formally approved in Norway.

New Market – May 20, 2026

Lundbeck receives orphan drug designation in Japan 

The orphan drug designation has been granted for asedebart for the treatment of patients with congenital adrenal hyperplasia and Cushing’s disease.

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Related posts

Financing - May 22, 2026

Neobiomics receives investment from HealthCap

The company has announced an investment led by HealthCap, and conjunction with this capital infusion, Neobiomics strengthens its board with the appointment of a new director, Mårten Steen, Managing Partner at HealthCap. 

Collaboration - May 20, 2026

Western Sweden unites to boost life sciences competitiveness

Industry, academic, and public stakeholders will join forces in a new council aimed at accelerating the region's life science development.

Clinical Trials - May 20, 2026

Oncopeptides secures regulatory approval to start Window-of-Opportunity study

Oncopeptides' clinical trial application for the "Window-of-Opportunity" (WoO) study in glioblastoma has been formally approved in Norway.

New Market - May 20, 2026

Lundbeck receives orphan drug designation in Japan 

The orphan drug designation has been granted for asedebart for the treatment of patients with congenital adrenal hyperplasia and Cushing’s disease.

CDMO - May 20, 2026

Diamyd Medical receives GMP certification and manufacturing authorization

The company has now received GMP (Good Manufacturing Practice) certification as well as manufacturing authorization from the Swedish Medical Products Agency for the production of biological investigational medicinal products for human use.

Collaboration - May 20, 2026

Herantis Pharma partners with Indivi

Herantis Pharma has announced a collaboration with Indivi, a Basel-based TechBio company focused on advancing precision medicine in neuroscience drug development, to integrate Indivi's digital biomarker platform into Herantis' upcoming Phase 2 proof-of-concept study of HER-096 in people living with Parkinson's disease.

Clinical Trials - May 19, 2026

Orexo announces positive outcome from an in-vivo study

Orexo has announced positive data from a pre-clinical in-vivo study on the nasal absorption of atipamezole when delivered with Orexo’s AmorphOX drug delivery technology.

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