Home Sanofi Acquires Vigil Neuroscience for $470 Million to Add Oral TREM2 Agonist VG-3927 to Neurology Pipeline

Sanofi Acquires Vigil Neuroscience for $470 Million to Add Oral TREM2 Agonist VG-3927 to Neurology Pipeline

May 22, 2025 15:24 CST Updated 15:24
Vigil Neuroscience

Neurodegenerative Disease Treatment New Drug Developer

Sanofi

Pharmaceutical R&D Developer

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Local time on May 22, Sanofi announced that it had reached an agreement to acquireVigil Neuroscience, Inc., obtaining the latter's product for treatmentAlzheimer's Disease(AD)Oral small moleculeVG-3927Vigil Neuroscience's Second Molecular ProjectVGL101 was not acquired.), this acquisition will enhance Sanofi's presence inNeurology FieldThe early R&D pipeline.
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Screenshot source: Corporate official website
According to the terms of the agreement, Sanofi will acquire all outstanding common shares of Vigil Neuroscience, Inc. for $8 per share in cash at the closing of the transaction, with an equity value of approximately$470 million(Calculated after complete dilution).
In addition, Vigil's shareholders will receive non-transferable contingent value rights for each share of Vigil stock. (CVR), which will entitle the holder to a $2 deferred cash payment upon the first commercial sale of VG-3927.
It is worth mentioning that this is not the first collaboration between the two companies. In June 2024, Sanofi had previously collaborated with...Vigil Neuroscience Conducts$40 millionThe strategic investment includes the exclusive right to prioritize negotiations for the research, development, production, and commercialization exclusive license, grant, or transfer of VG-3927.
VG-3927 is aSpeciesOral Small Molecule TREM2 Agonist, activating TREM2 is expected to enhance the neuroprotective function of microglia in Alzheimer's disease. This drug has currently completed a Phase I clinical trial.NCT06343636)
InAt the 2025 AD/PD International Conference,Vigil Neuroscience, Inc. announced positive results of the trial in an oral presentation. The data showed:
  • VG-3927 Exhibits Predictable and Dose-Dependent Pharmacokinetics (PK) Features, SupportOnce daily dosing. At the same time, VG-3927 has high central nervous system permeability.

  • The PK and sTREM2 reduction observed in the single-dose AD cohort were consistent with those in healthy volunteers, as well as across different genotypes of AD patients.TREM2 andApoE Gene Variation)ChinasTREM2 ReductionAre similar.

  • At a dose of 25 mg, VG-3927 achieved levels in the cerebrospinal fluidThe maximum reduction in sTREM2 was approximately 50%.

  • PK/PD data support the selection in Phase II trials for AD patients25 mg once daily oral dose

  • VG-3927 in all populations(Healthy volunteers, elderly participants, AD patients)Both exhibited good safety and tolerability, with no serious adverse events occurring.

  • All treatment-related adverse events(AE)All were mild or moderate and resolved on their own.

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