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BioWorld - Saturday, July 4, 2026
Home » Parkinson’s disease

Articles Tagged with ''Parkinson’s disease''

Illustration of double helix
Newco news

Taking on gene delivery, Coave raises $33M series A

Jan. 9, 2025
By Nuala Moran
Coave Therapeutics SA has completed the transition to becoming a genetic medicines specialist, after divesting its single ophthalmology program and raising $33 million in a series A round.
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Scientist, microscope and dropper
Neurology/psychiatric

Acadia presents preclinical characterization of ACP-204

Dec. 24, 2024
Pimavanserin is a 5-HT2A inverse agonist that is FDA approved for treating Parkinson’s disease psychosis. Acadia Pharmaceuticals Inc. searched for a compound that relies on pimavanserin but with an improved profile, including shorter half-life and reduced QT prolongation risk, which led to the identification of ACP-204.
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Omeros, Prothena stocks climb on clinical data; Vertex slips

Dec. 19, 2024
By Karen Carey
Clinical data reported by a handful of biopharmas on Dec. 19 sent stocks soaring or plunging, as company leaders laid out next-step plans. Investors showed enthusiasm for Omeros Corp.’s narsoplimab to treat hematopoietic stem cell-transplant-associated thrombotic microangiopathy (TA-TMA), and Roche AG’s Parkinson’s prospect prasinezumab, which is partnered with Prothena Corp. plc.
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Diagnostics

Researchers in the Netherlands describe new PET and SPECT imaging agents

Dec. 11, 2024
Researchers at Stichting AMC Foundation and Vrije Universiteit van Amsterdam have identified [18F]-labeled pyrazolidine-3,5-dione compounds targeting P2Y purinoceptor 12 (P2RY12; P2Y12) acting as PET and SPECT imaging agents. They are reported to be useful for the diagnosis of multiple sclerosis, Alzheimer’s disease and Parkinson’s disease.
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Brain and DNA
Neurology/psychiatric

Spur Therapeutics selects gene therapy development candidate for Parkinson’s disease with GBA1 mutations

Dec. 4, 2024
Spur Therapeutics Ltd. has selected SPR-301 as lead development candidate from its gene therapy program for a genetically defined subset of Parkinson’s disease characterized by mutations in the GBA1 gene. The mutations cause a deficiency in the enzyme glucocerebrosidase (GCase), leading to the accumulation of α-synuclein and subsequent death of neuronal cells that are hallmarks of Parkinson’s disease.
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Hands holding brain
Neurology/psychiatric

Rome Therapeutics’ LINE-1 RT inhibitors show neuroprotective effect in Parkinson’s disease models

Nov. 22, 2024
Rome Therapeutics Inc. has presented data demonstrating the potential of its LINE-1 reverse transcriptase (RT) inhibitors.
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Parkinson's disease illustration showing neurons containing alpha-synuclein
Neurology/psychiatric

GPR40 as a promising new target for Parkinson’s disease

Nov. 18, 2024
Scientists at Gachon University and their collaborators investigated the neuroprotective effects of the GPR40 agonist TUG-469 in models of Parkinson’s disease (PD).
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John Mendlein, executive chairman and interim CEO, Vesalius
Neurology/psychiatric

Vesalius-GSK $650M pact: Targeting Parkinson’s root causes

Nov. 13, 2024
By Karen Carey
More than two years since emerging from stealth, Vesalius Therapeutics Inc. signed its first major pharma deal with GSK plc. Worth up to $650 million and possibly more if an option is exercised, the multitarget alliance aims to discover and develop novel treatments for Parkinson’s disease and another neurodegenerative indication.
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John Mendlein, executive chairman and interim CEO, Vesalius

Vesalius-GSK $650M pact: Targeting Parkinson’s root causes

Nov. 12, 2024
By Karen Carey
More than two years since emerging from stealth, Vesalius Therapeutics Inc. signed its first major pharma deal with GSK plc. Worth up to $650 million and possibly more if an option is exercised, the multitarget alliance aims to discover and develop novel treatments for Parkinson’s disease and another neurodegenerative indication.
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Neurology/psychiatric

NRG selects Parkinson’s development candidate

Oct. 31, 2024
NRG Therapeutics Ltd., has nominated NRG-5051 as its first development candidate, and secured a $5 million grant from the Michael J. Fox Foundation for Parkinson’s Research (MJFF) to support its preclinical development of as a disease-modifying treatment for Parkinson’s disease.
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