Essential Pharma acquires Reminyl from Janssen Pharmaceutica

Phase 2Cell TherapyAcquisitionPhase 1
Essential Pharma acquires Reminyl from Janssen Pharmaceutica
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Source: Pharmaceutical Technology
Reminyl is intended to treat mild to moderately severe dementia of the Alzheimer type. Credit: Hryshchyshen Serhii / Shutterstock.com.
Speciality pharmaceutical group Essential Pharma has concluded the acquisition of Reminyl oral capsules from Johnson & Johnson company Janssen Pharmaceutica.
The strategic move enhances Essential Pharma’s portfolio of central nervous system (CNS) medicines and expands its global footprint, particularly in Asia-Pacific.
A cholinesterase inhibitor, Reminyl is an established CNS drug for mild to moderately severe dementia of the Alzheimer type.
Essential Pharma will now hold rights to Reminyl in the European Economic Area, South Korea, Thailand and all other existing markets for this product.
The deal excludes the UK and Ireland, Japan and Latin America.
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Essential Pharma acquires Reminyl from Janssen Pharmaceutica
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Source: Pharmaceutical Technology
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Essential Pharma acquires Reminyl from Janssen Pharmaceutica
Preview
Source: Pharmaceutical Technology
The acquisition aligns with Essential Pharma’s focus on CNS, gastroenterology, ophthalmology and rare diseases.
Essential operates in more than 70 countries and is supported by healthcare investment firm Gyrus Capital.
Essential CEO Emma Johnson stated: “Our acquisition of rights to Reminyl in these markets will ensure Alzheimer’s patients and caregivers in those regions have continued access to this vital medicine.
“The acquisition represents a significant and synergistic addition to our concentrated portfolio of CNS products, further expanding our global presence and solidifying our position as a leading speciality pharma group.”
The latest development comes after Essential Pharma acquired clinical-stage pharmaceutical company Renaissance Pharma for an undisclosed sum in April 2024.
Renaissance develops treatments for paediatric rare diseases, with its lead asset, Hu14.18K322A, currently being analysed in a Phase II clinical trial to treat high-risk neuroblastoma.
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