E2025
/ Eisai
- LARVOL DELTA
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December 25, 2025
Drug Development.
(PubMed, Alzheimers Dement)
- "SILK technology demonstrated that E2025 increased the turnover rate of EphA4 in a concentration-dependent manner. Therefore, this method may be applicable for assessing the pharmacodynamic effects of E2025. References [1] Verma, M., Chopra, M. & Kumar, H. Cell Mol Neurobiol 43, 3375-3391, (2023). [2] Vargas, L. M., Cerpa, W., Munoz, F. J., Zanlungo, S. & Alvarez, A. R. Biochim Biophys Acta Mol Basis Dis 1864, 1148-1159, (2018)."
Journal • Alzheimer's Disease • CNS Disorders • EPHA4
January 12, 2025
Developing Topics.
(PubMed, Alzheimers Dement)
- "E2025 specifically suppresses the EphA4 pathway via multiple modes of action, and suppresses progression of tau pathology in a transgenic tau model of AD."
Journal • Alzheimer's Disease • CNS Disorders • EPHA4
June 20, 2024
E2025, a novel anti-EphA4 antibody, enhances EphA4 cleavage, and suppresses tau pathologies in a transgenic model of AD
(AAIC 2024)
- "E2025 specifically suppresses the EphA4 pathway via multiple modes of action, and suppresses progression of tau pathology in a transgenic tau model of AD."
Alzheimer's Disease • CNS Disorders • EPHA4
March 25, 2024
A Study to Assess the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Pharmacodynamics of E2025 in Healthy Participants
(clinicaltrials.gov)
- P1 | N=32 | Completed | Sponsor: Eisai Inc. | Recruiting ➔ Completed
Trial completion
February 28, 2023
A Study to Assess the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Pharmacodynamics of E2025 in Healthy Participants
(clinicaltrials.gov)
- P1 | N=41 | Recruiting | Sponsor: Eisai Inc. | Not yet recruiting ➔ Recruiting
Enrollment open
February 14, 2023
A Study to Assess the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Pharmacodynamics of E2025 in Healthy Participants
(clinicaltrials.gov)
- P1 | N=41 | Not yet recruiting | Sponsor: Eisai Inc.
New P1 trial
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