InvestigationalCognitiveIntranasalEvidence 2/5

Davunetide

Also known as: NAP, AL-108, CP201

Davunetide binds microtubule end-binding proteins to promote microtubule stability and the tau-microtubule interaction, reducing tau hyperphosphorylation in preclinical models.

Davunetide
Drug class
ADNP-derived microtubule-stabilizing neuroprotective peptide
Primary targets
Microtubules, Tubulin, Microtubule end-binding proteins EB1/EB3, Tau protein
Dose reference
Investigational; no approved dose. Trial regimens (not recommendations) used intranasal NAP roughly 5-15 mg in MCI studies and 30 mg twice daily in the phase 2/3 PSP trial.
Half-life
Short; preclinical estimates of roughly 15 minutes in brain after intranasal dosing. Human pharmacokinetics were not characterized in the pivotal PSP trial.
Developer / origin
Allon Therapeutics (NAP/ADNP discovery by Illana Gozes and colleagues, Tel Aviv University); CP201 program for ADNP syndrome
Reference year
1999
Evidence score
2/5 - Weak / negative pivotal evidence
Evidence 2/5

Weak / negative pivotal evidence

Davunetide has well-characterized preclinical microtubule and tau biology, but its largest human trial failed and no study has established clinical efficacy in any indication.

Mostly animal, ex vivo, cell, or indirect evidence.

Evidence basis

  • 313-patient randomized, double-blind, placebo-controlled phase 2/3 PSP trial (Boxer et al., Lancet Neurology 2014) showed no benefit on co-primary endpoints (PSPRS p=0.72)
  • Phase 2 schizophrenia trial: cognition (MCCB) not significant vs placebo; only a functional-capacity (UPSA) signal
  • Mechanistic 3R vs 4R tau isoform preference may explain PSP failure
  • No FDA approval; investigational repositioning as CP201 for ADNP syndrome lacks a completed pivotal efficacy trial

How to read this entry

Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.

Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.

Davunetide guides

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