We share our latest development updates, scientific publications and industry perspectives

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Neumirna Strengthens Board with Andreas Wallnöfer as Independent Board Member
Neumirna Therapeutics has named Andreas Wallnöfer as an independent member of its Board of Directors.
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Lina's Story: In Honor of World Parkinson's Day
"When the doctor told me she suspected it might be Parkinson's, I responded, 'That can't be right. I don’t even tremble." Today, on World Parkinson’s Day, we’re honored to share Lina’s story – an intimate and honest glimpse into the daily reality of living with this complex condition.
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Neumirna Therapeutics secures €20M to develop RNA therapies
Neumirna Therapeutics secures €20M in Series A financing to develop RNA therapies for epilepsy and other neurological disorders
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Nobel Prize 2024 Awarded for Discovery of microRNAs
This year’s Nobel Prize in Physiology or Medicine recognizes the discovery of microRNAs. These small RNA molecules are central to Neumirna Therepeutics approach to developing treatments for neurological diseases.
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New Review by Neumirna Team Explores Nrf2 as a Promising Target in Neurodegeneration
A new review article based on the work led by Clara Mayer and Lluís Riera-Ponsati from Neumirna Therepeutics has been published in Frontiers in Pharmacology.
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Neumirna Therapeutics Secures Third Innobooster Grant of 5 Million DKK to Propel Epilepsy Disease-Modifying Therapy to the Clinic
This substantial funding will be allocated to advance Neumirna's groundbreaking disease-modifying therapy for epilepsy to the clinic, bringing hope to the circa 50 million patients affected by epilepsy worldwide.
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Review on Adenosine in the treatment of neuropathic pain published in the Scandinavian Journal of Pain
Henrik Klitgaard (Co-Founder, PhD) and Stine Norman-Hansen (Senior Scientist, PhD) authored this topical review together with leading pain expert, Prof. Lars Arendt-Nielsen.
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Neumirna Wins Nordic Star Award at NLS Days 2023
Neumirna has been awarded the Nordic Star Award at NLS Days 2023, recognizing the company as the start-up with the highest investment potential.
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NEUmiRNA featured on MedWatch: “RNA startup from Copenhagen begins hunting for large capital raising”
With a new CEO in place, Sunstone-backed Neumirna aims to land a three-digit million sum in the first half of 2024.
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Critical Review from Neumirna Team Published in Epilepsia
A new critical review by the Neumirna Therepeutic team has been published in Epilepsia, the leading journal in epilepsy research and clinical care.
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Neumirna awarded a Eureka Network EUROSTARS grant of 1.65M€ in collaboration with Motac Neuroscience Ltd, the Université de Bordeaux and the Center for RNA Medicine!
This grant will enable us to develop innovative RNA therapies which could revolutionize the treatment of Parkinson's Disease.
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3-year Industrial Postdoc Fellowship awarded to Lluís Riera-Ponsatí
This grant from the Innovation Fund Denmark (IFD) will help us in further establishing our drug discovery pipeline, aimed at developing disease-modifying RNA Therapies for Parkinson's Disease at NEUmiRNA, in collaboration with Aalborg University and the Center for RNA Medicine (CRM).
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Neumirna Receives $650,000 Grant from The Michael J. Fox Foundation to Advance RNA Therapies for Parkinson’s Disease
The project, conducted in collaboration with Motac Neuroscience and the Center for RNA Medicine at Aalborg University, aims to accelerate the development of disease-modifying treatments targeting microRNAs in Parkinson’s disease.
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New publication on RNA Biology
A comprehensive review on RNA Therapeutics for the treatment of neurmouscular disorders is out now on the latest issue of RNA Biology.
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Neumirna at the EVF global accelerator course
In 2021, Neumirna was selected and awarded by the US Epilepsy Foundation as being a promising start-up to advance new treatments for people with epilepsy in the EVF global accelerator course for start-up companies.
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Review of the potential of targeting the Nrf2 pathway for neurodegeneration published in Frontiers of Pharmacology
Janine joined Neumirna from Pfizer, where he served as senior vice president and chief scientific officer of the Rare Disease Research Unit.
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