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Research compendium

Davunetide

Davunetide, also known as NAP or AL-108, has been studied in preclinical neuronal-disorder models and human research. Its documentation includes favorable mouse findings and a negative controlled trial in progressive supranuclear palsy. Both must remain visible.

This is a research reference, not a product offered in the Asciende catalog. Published studies do not establish the identity, purity or availability of a commercial preparation.

Sequence origin and measured compartment

Do not turn a name’s origin into a localization or function claim. Preserve the specific evidence connecting sequence, detection and response.

  • Does the work distinguish a proposed sequence, detected peptide and synthesized material?
  • Which compartment or model supplies the signal being interpreted?
  • Is the functional readout compared with appropriate system controls?

Mechanism described in the literature

NAP’s preclinical hypothesis concerns the microtubule system. Animal behavioral or protein-accumulation changes do not alone prove direct molecular interaction or necessarily explain a human trial’s outcome.

Classification

Synthetic research peptide

Other names

  • Davunetide
  • NAP
  • AL-108

The alpha-synuclein model

In mice overexpressing human alpha-synuclein, NAP was associated with fewer motor-test errors and differences in proteinase-K-resistant inclusions. Findings concern that genetic construct and those outcomes, not every disease involving altered neuronal proteins.

The trial that did not confirm benefit

The randomized trial in people with progressive supranuclear palsy found no placebo difference in primary progression and daily-activity endpoints. Preclinical findings therefore cannot be presented as confirmation of human benefit in that disease.

Why the findings are not interchangeable

The mouse study and human trial examined different pathological systems and variables, so they are not direct replications. A rigorous account separates mechanistic plausibility, animal behavior and human outcomes, retaining the negative finding without turning it into a conclusion about every possible experimental context.

Questions and answers

Was the human trial positive?

Not for the primary endpoints evaluated in progressive supranuclear palsy.

Does the mouse motor test predict the human outcome?

Not by itself. Species, pathological model and measured variable differ.

Sources

  1. A pilot trial of the microtubule-interacting peptide (NAP) in mice overexpressing alpha-synuclein shows improvement in motor function and reduction of alpha-synuclein inclusions. — Mol Cell Neurosci (2011); PMID 21193046; DOI 10.1016/j.mcn.2010.12.011
  2. A pilot trial of the microtubule-interacting peptide (NAP) in mice overexpressing alpha-synuclein shows improvement in motor function and reduction of alpha-synuclein inclusions. — Mol Cell Neurosci (2011); PMID 21193046; DOI 10.1016/j.mcn.2010.12.011
  3. Davunetide in patients with progressive supranuclear palsy: a randomised, double-blind, placebo-controlled phase 2/3 trial. — Lancet Neurol (2014); PMID 24873720; DOI 10.1016/S1474-4422(14)70088-2
  4. Davunetide in patients with progressive supranuclear palsy: a randomised, double-blind, placebo-controlled phase 2/3 trial. — Lancet Neurol (2014); PMID 24873720; DOI 10.1016/S1474-4422(14)70088-2
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