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Name: Buntanetap
Synonyms: Posiphen, ANVS-401, Posiphen tartrate
Chemical Name: (3aR)-1, 3a, 8-trimethyl-1, 2, 3, 3a, 8, 8a-hexahydropyrrolo (2, 3-b) indol-5-yl phenyl-carbamate tartrate
Therapy Type: Small Molecule (timeline)
Target Type: Amyloid-Related (timeline), alpha-synuclein
Condition(s): Alzheimer's Disease, Parkinson's Disease
U.S. FDA Status: Alzheimer's Disease (Phase 2), Parkinson's Disease (Phase 1/2)
Company: Annovis Bio


Buntanetap, previously known as posiphen or ANVS-401, is the pure (+) enantiomer, i.e. mirror image, of phenserine. Both compounds derive from the intramural research program at NIH and were licensed to Axonyx, Inc., which developed both enantiomers into the clinic. Axonyx merged with Torrey Pines Therapeutics, which licensed posiphen to QR Pharma in 2008.

Both posiphen and phenserine reduce production of amyloid precursor protein by blocking translation of its mRNA (Shaw et al., 2001). Phenserine also inhibits acetylcholinesterase, while posiphen does not. Both are dosed by mouth and enter the brain. Posiphen and phenserine are considered separate therapeutics, as there is no chiral switching between the two, or between their metabolites. Posiphen and phenserine, and their respective metabolites, differ in their pharmacokinetics.

They share a number of common actions and, additionally, have separate actions. Posiphen and phenserine act on iron-response element sequences in the 5' untranslated region of APP mRNA to inhibit APP protein synthesis. They reduced APP and Aβ in neuronal cultures and brains of wild-type and AD transgenic mice (Lahiri et al., 2007; Marutle et al., 2007). Both drugs were reported to be neuroprotective and neurotrophic in AD mouse models (Lilja et al., 2013; Lilja et al., 2013), and posiphen was reported to normalize memory impairment, learning, and synaptic function (Teich et al., 2018). Posiphen was also tested in the APP-overexpressing Ts65DN mouse model of Down's syndrome, where 50 mg/kg for 26 days lowered expression of APP and its C-terminal fragments, corrected deficits in axonal transport, and normalized neurotrophin signaling (Chen et al., 2021).

Posiphen and phenserine reportedly also block translation of α-synuclein mRNA, implying potential application in Parkinson’s disease (Rogers et al., 2011Mikkilineni et al., 2012; Yu et al., 2013). Posiphen reduced α-synuclein expression in brain and gut, and improved intestinal function in the A53T α-synuclein transgenic mouse model of PD (Kuo et al., 2019).

Posiphen was reported to improve outcomes in rodent stroke models (Yu et al., 2020) and to augment neurogenesis post stroke Turcato et al., 2018).


Results of three Phase 1 studies of posiphen are published (Maccecchini et al., 2012). They include single and multiple dosing in 120 healthy adults and a small proof-of-concept study in five people with MCI. Most common side effects were dizziness, nausea, and vomiting that increased with dose. Adverse effects did not increase significantly at doses of up to 60 mg four times a day for 10 days, at which point posiphen reached brain concentrations presumed sufficient to inhibit APP production. Ten days of treatment in people with MCI led to statistically significant reductions in CSF of APP cleavage fragments sAPPα and β, as well as of both total- and phosphorylated-tau, and the inflammation markers YKL-40, complement C3, and MCP-1. A trend for reduction was evident in CSF levels of Aβ42 (-51.4%, p=0.0533).

In March 2017, QR Pharma started a Phase 1/2 trial to study the effect of posiphen on APP synthesis in people with early AD. The study is recruiting 24 participants with a diagnosis of amnestic MCI or probable mild AD, and CSF levels of Aβ42 consistent with AD. They are randomized to receive 60, 120, or 180 mg daily, divided into three doses, or placebo for 23 to 25 days. Primary endpoints are safety, pharmacokinetics in plasma and CSF, and the rate of turnover of CSF Aβ40 using the stable isotope labeling kinetics (SILK) technique (see Paterson et al., 2019). The Alzheimer Disease Cooperative Study group is running the trial at six academic medical centers in the U.S. As of February 2020, 11 participants had enrolled, and no adverse effects were reported (company press release). The trial was paused from March to October 2020 due to COVID19, and was completed in December 2021 with 18 participants. Results are posted on In 2019, QR Pharma became Annovis Bio.

In August 2020, Annovis began a Phase 1/2 dose-finding biomarker study in early AD and Parkinson’s disease patients. In Part 1, 14 AD and 14 PD patients were to be randomized roughly 2:1 to 80 mg posiphen or placebo, taken daily for 23 to 27 days. At the last dose, participants undergo blood and CSF sampling. In Part 2 of the study, 40 PD patients will receive 5, 10, 20, 40 or 80 mg posiphen, under the same design as in Part 1. The primary outcome is adverse events. Other endpoints include pharmacokinetic, functional, and cognitive endpoints. A panel of CSF biomarkers to be measured spans amyloid and tau pathology, inflammation, and neuronal death.

Part 1 finished in early 2021, and Annovis presented results at the 2021 AAIC on July 28. There were no serious adverse events. On exploratory efficacy measures, the company claimed a statistically significant within-subject improvement in the ADAS-Cog11 from baseline to 25 days, but the comparison with placebo group fell short of significance. Posiphen-treated PD patients improved on the WAIS coding task, a paper-and-pencil test measuring motor dexterity and cognitive speed compared to placebo. The AD patients had a decrease in all amyloid/tau biomarkers, with a 12 percent reduction in pTau, and improvement in the Aβ42/40 ratio. The neurodegeneration biomarker NfL had 13 percent lower levels in AD and 9 percent in PD, but the change was not statistically significant. The company reported significant reductions by 43 and 28 percent in inflammatory markers sTREM2 and GFAP in treated PD patients; a 55 percent YKL40 reduction did not meet statistical significance. The study finished in January 2022. Full results report improvement on the MDS-UPDRS and WAIS coding in PD patients, with optimal responses occurring at 10-20 mg (Fang et al., 2023).

In August 2022, the company began a large Phase 3 study in people with early PD. The study intends to enroll 450 participants for six months of 10 or 20 mg buntanetap daily, or placebo, with a primary outcome of MDS-UPDRS Parts 2 and 3 (activities of daily living and motor exam), and safety. Other outcomes include total MDS-UPDRS total score, clinician and patient impression of change, WAIS, and biomarkers. The study plans to run at approximately 100 locations in the U.S. and Europe until December 2023.

In April 2023, the company started a Phase 2/3 trial in mild to moderate AD. The dose ranging study plans to randomize 320 participants to 7.5, 15, or 30 mg buntanetap or placebo, once daily for three months. Primary outcomes are ADAS-Cog11 and the ADSC-CGIC. Other outcomes include the ADCS-ADL, MMSE, and the Digit Symbol Substitution Test. The trial is expected to run at 80 sites in the U.S. until February 2024.

For details on posiphen trials, see

Last Updated: 26 May 2023


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Therapeutics Citations

  1. Phenserine

Paper Citations

  1. . Posiphen as a candidate drug to lower CSF amyloid precursor protein, amyloid-β peptide and τ levels: target engagement, tolerability and pharmacokinetics in humans. J Neurol Neurosurg Psychiatry. 2012 Sep;83(9):894-902. PubMed.
  2. . SILK studies - capturing the turnover of proteins linked to neurodegenerative diseases. Nat Rev Neurol. 2019 Jul;15(7):419-427. Epub 2019 Jun 20 PubMed.
  3. . Buntanetap, a Novel Translational Inhibitor of Multiple Neurotoxic Proteins, Proves to Be Safe and Promising in Both Alzheimer's and Parkinson's Patients. J Prev Alzheimers Dis. 2023;10(1):25-33. PubMed.
  4. . Phenserine regulates translation of beta -amyloid precursor protein mRNA by a putative interleukin-1 responsive element, a target for drug development. Proc Natl Acad Sci U S A. 2001 Jun 19;98(13):7605-10. PubMed.
  5. . The experimental Alzheimer's disease drug posiphen [(+)-phenserine] lowers amyloid-beta peptide levels in cell culture and mice. J Pharmacol Exp Ther. 2007 Jan;320(1):386-96. PubMed.
  6. . Modulation of human neural stem cell differentiation in Alzheimer (APP23) transgenic mice by phenserine. Proc Natl Acad Sci U S A. 2007 Jul 24;104(30):12506-11. PubMed.
  7. . Neurotrophic and neuroprotective actions of (-)- and (+)-phenserine, candidate drugs for Alzheimer's disease. PLoS One. 2013;8(1):e54887. PubMed.
  8. . Age-dependent neuroplasticity mechanisms in Alzheimer Tg2576 mice following modulation of brain amyloid-β levels. PLoS One. 2013;8(3):e58752. PubMed.
  9. . Translational inhibition of APP by Posiphen: Efficacy, pharmacodynamics, and pharmacokinetics in the APP/PS1 mouse. Alzheimers Dement (N Y). 2018;4:37-45. Epub 2018 Jan 18 PubMed.
  10. . Targeting increased levels of APP in Down syndrome: Posiphen-mediated reductions in APP and its products reverse endosomal phenotypes in the Ts65Dn mouse model. Alzheimers Dement. 2021 Feb;17(2):271-292. Epub 2020 Sep 25 PubMed.
  11. . The alpha-synuclein 5'untranslated region targeted translation blockers: anti-alpha synuclein efficacy of cardiac glycosides and Posiphen. J Neural Transm. 2011 Mar;118(3):493-507. PubMed.
  12. . The anticholinesterase phenserine and its enantiomer posiphen as 5'untranslated-region-directed translation blockers of the Parkinson's alpha synuclein expression. Parkinsons Dis. 2012;2012:142372. PubMed.
  13. . Synthesis of the Alzheimer drug Posiphen into its primary metabolic products (+)-N1-norPosiphen, (+)-N8-norPosiphen and (+)-N1, N8-bisnorPosiphen, their inhibition of amyloid precursor protein, α-synuclein synthesis, interleukin-1β release, and cholinergi. Antiinflamm Antiallergy Agents Med Chem. 2013 Jan 22; PubMed.
  14. . Translational inhibition of α-synuclein by Posiphen normalizes distal colon motility in transgenic Parkinson mice. Am J Neurodegener Dis. 2019;8(1):1-15. Epub 2019 Feb 15 PubMed.
  15. . Post-treatment with Posiphen Reduces Endoplasmic Reticulum Stress and Neurodegeneration in Stroke Brain. iScience. 2020 Feb 21;23(2):100866. Epub 2020 Jan 28 PubMed.
  16. . Sequential combined Treatment of Pifithrin-α and Posiphen Enhances Neurogenesis and Functional Recovery After Stroke. Cell Transplant. 2018 Apr;27(4):607-621. Epub 2018 Jun 5 PubMed.

External Citations

  1. company press release

Further Reading


  1. . Alzheimer's Disease and Its Potential Alternative Therapeutics. J Alzheimers Dis Parkinsonism. 2019;9(5) Epub 2019 Sep 13 PubMed.
  2. . Novel 5' untranslated region directed blockers of iron-regulatory protein-1 dependent amyloid precursor protein translation: implications for down syndrome and Alzheimer's disease. PLoS One. 2013;8(7):e65978. PubMed.
  3. . Phenserine. Expert Opin Investig Drugs. 2007 Jul;16(7):1087-97. PubMed.
  4. . In Silico and Ex Vivo Analyses of the Inhibitory Action of the Alzheimer Drug Posiphen and Primary Metabolites with Human Acetyl- and Butyrylcholinesterase Enzymes. ACS Pharmacol Transl Sci. 2022 Feb 11;5(2):70-79. Epub 2022 Jan 12 PubMed.
  5. . A pilot exploration with Posiphen to normalize amyloid precursor protein in Down syndrome. Neural Regen Res. 2021 Dec;16(12):2420-2421. PubMed.