Standard Dosage Range
Research dosing range: 6–30 mg daily (intranasal)
Educational reference only
Dosage by Use Case
Amnestic Mild Cognitive Impairment (aMCI)
12 months
Dose used in Phase II clinical trials showing cognitive benefits. Administered via intranasal spray.
Progressive Supranuclear Palsy (PSP)
52 weeks
Dose used in failed Phase II/III trial. While ineffective for PSP overall, subgroup analysis suggested potential benefits in certain patients.
ADNP Syndrome
Ongoing
Dosing varies based on patient age, weight, and symptom severity. Administered intranasally. Requires close monitoring by a physician specialized in ADNP syndrome.
Cognitive Enhancement (Experimental)
4-8 weeks
Intranasal administration. Limited human data exists outside of clinical trials. Consider starting at lower end of range.
Timing & Frequency
Davunetide is typically administered intranasally in the morning or evening. The timing may be adjusted based on individual preferences and tolerance.
Cycle Guidance
Clinical trials have used davunetide for up to 12 months. Cycling is not strictly necessary but may be considered to assess ongoing efficacy and minimize potential long-term effects. Consult with a healthcare professional for personalized guidance.
Reconstitution Reference
Quick reference for reconstituting Davunetide. For custom vial sizes and concentrations, use the Reconstitution Calculator.
| Common Vial Size | Typically supplied as a pre-filled nasal spray |
| BAC Water Volume | N/A (pre-filled spray) |
| Concentration & Draw | Concentration varies depending on the formulation (typically provides a specific mg dose per spray) |
| Storage | Store at recommended temperature per manufacturer instructions, typically refrigerated or at room temperature. |
| Stability | Follow manufacturer expiry date on the packaging. |
Frequently Asked Questions
What is the standard davunetide dosage for cognitive impairment?
How is davunetide administered?
What are the potential side effects of davunetide?
Last updated: 2026-02-19