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PreclinicalResearch compoundModerate evidence

ACD856

Pan-Trk positive allosteric modulator (AlzeCure) that amplifies BDNF/NGF signaling, with Phase 1 human data.

NootropicTrk modulatorBDNFMemoryBDNFnoo.affects.memorynoo.affects.neuroprotection

Pharmacology

ClassBDNF · Memory
Primary targetTrk receptor positive allosteric modulation
Targets3 receptor targets
Half-lifeApproximately 19 to 20 hours (human Phase 1 PK)
OnsetMorning dosing recommended (plasticity and mood effects); in clinical development
EvidenceModerate evidence
Affected systemsBDNFnoo.affects.memorynoo.affects.neuroprotection

Contents

WHAT IS ACD856?

Detailed overview

ACD856 (AlzeCure Pharma) is a triazinetrione-class, orally active, pan-Trk positive allosteric modulator (PAM) that potentiates the tropomyosin receptor kinase family (TrkA, TrkB, TrkC). It does not activate the receptor directly; instead it amplifies signaling triggered by the body's own neurotrophins (BDNF, NGF), so it acts only where an endogenous signal is already present. In preclinical models it improved memory, produced antidepressant-like effects, and showed neuroprotective, disease-modifying effects. In completed Phase 1 (single and multiple ascending dose) human trials it was well tolerated, with a half-life of roughly 19 to 20 hours and a pro-cognitive signature on quantitative EEG. A Phase 2 trial is planned for Alzheimer's disease; depression, sleep disorders, and traumatic brain injury indications remain at the preclinical stage.

Mechanism

Pan-Trk PAM (amplifies BDNF/NGF signaling)

Evidence

Phase 1 human safety + PK, preclinical efficacy

Legal status

Investigational (unapproved) drug

Receptor profile

  • TrkA / TrkB / TrkC receptorsStrong
  • BDNF and NGF neurotrophin signalingStrong
  • PI3K/Akt and MAPK/ERK downstream cascadesModerate

Safety

Side effects, stop signs, contraindications

Side effects · 5

  • Well tolerated in Phase 1 human trials with no serious adverse events reported
  • Mild, transient headache is possible
  • Mild nausea or gastrointestinal discomfort may occur
  • Long-term safety in patient populations remains unestablished (ongoing development)
  • Theoretical risks of Trk signaling (e.g. modulation of pain signaling) are not yet fully characterized in humans

Contraindications · 4

  • Pregnancy and breastfeeding: safety not established, avoid
  • Investigational, unapproved drug; not recommended outside clinical supervision
  • Effect of co-administration with other agents affecting neurotrophin signaling is unknown
  • Theoretical caution warranted with known Trk-dependent malignancy given the amplification of neurotrophin signaling

Related Nootropics

Same therapeutic category

Studies

Related research and clinical findings

FAQ

FAQ

Pan-Trk positive allosteric modulator (AlzeCure) that amplifies BDNF/NGF signaling, with Phase 1 human data.

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Structure & chemistry

TypeNootropic
UpdatedJuly 10, 2026
MolekulaX Editorial Team·Source-verified · PubMed · FDA · EMA
Updated: July 10, 2026

The information here is strictly for educational and scientific purposes. It does not replace medical advice or clinical consultation, and it does not encourage illegal substance or pharmaceutical use. Data is sourced. When in doubt, consult your doctor.