Drugs / ABvac40
last change Oct 2023 re-read 3 minutes ago

ABvac40

Vaccine

Developed for
Alzheimer disease · cognitive impairment with or without cerebellar ataxia
Investigated by
Araclon Biotech S.L.

Trials 2

20142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT03113812 Jan 2014 → Jul 2015 Alzheimer disease Araclon Biotech S.L. Completed No outcome recorded
Phase 21 trial · 1 met primary
Phase 2 NCT03461276 Dec 2017 → Mar 2023 Alzheimer disease, cognitive impairment with or without cerebellar ataxia Araclon Biotech S.L. Completed Met primary

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2023-10-24 Grifols Therapeutics LLC Results Araclon Biotech Presents Positive Final Results from Phase 2 Clinical Study of ABvac40 Alzheimer’s vaccine at CTAD grifols.com ↗
Araclon Biotech, a Grifols Group company dedicated to the research and development of therapies and diagnostic methods applied to neurodegenerative diseases, today announced encouraging final results from its Phase 2 trial ( NCT03461276 ) of ABvac40, an active vaccine against the Aβ40 peptide, for the treatment of patients with early-stage Alzheimer's disease (AD).
2022-03-15 Grifols Therapeutics LLC Results Araclon Biotech advances in its innovative vaccine and diagnostic test for Alzheimer’s grifols.com ↗
Regarding the vaccine ABvac40, the principal data analyzed until now (Part A) are satisfactory in that they support the continuation of the trial’s extension phase (Part B).

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 3 sources stand behind the page.

FieldValueCited text
Known as ABvac40 ClinicalTrials.gov intervention name — accepted as the source's own label NCT03113812 ↗
1

NCT03461276 ↗

Modality Vaccine “We have developed the first active vaccine against the C-terminal end of Aβ40, ABvac40, and assessed its safety and tolerability in a phase I clinical trial.” PMID 29378651 ↗ Jan 2018
Route Subcutaneous “All treatments were administered subcutaneously at 4-week intervals.” PMID 29378651 ↗ Jan 2018