Evidence map›Paper›PMID 35243208›Full record

ArticleJournal of Alzheimer's disease reports2022

Robust Pharmacodynamic Effect of LY3202626, a Central Nervous System Penetrant, Low Dose BACE1 Inhibitor, in Humans and Nonclinical Species.

Brian A Willis, Stephen L Lowe, Scott A Monk, Patrick J Cocke, Christopher D Aluise, Leonard N Boggs, Anthony R Borders, Richard A Brier, Robert A Dean, Steven J Green and 11 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of Alzheimer's disease reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 3 institutions in 2 countries.

Brian A WillisLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Stephen L LoweLilly Centre for Clinical Pharmacology, Singapore, Singapore.
Scott A MonkLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Patrick J CockeLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Christopher D AluiseLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Leonard N BoggsLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Anthony R BordersLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Richard A BrierLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Robert A DeanLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Steven J GreenLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Douglas E JamesLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Stanford S JheePAREXEL International, Glendale, CA, USA.
Qun LinLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Albert C LoLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Patrick C MayLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Brian M WatsonLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Leonard L WinneroskiLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Zhixiang YangLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Jennifer A ZimmerLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
David L McKinzieLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Dustin J MergottLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Eli Lilly (United States) · USClinical Nutrition Research Centre · SGPAREXEL International (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe development of beta-site amyloid-beta precursor protein cleaving enzyme (BACE) 1 inhibitors for the treatment of Alzheimer's disease requires optimization of inhibitor potency, selectivity, and brain penetration. Moreover, there is a need for low-dose compounds since liver toxicity was found with some BACE inhibitors.

objectiveTo determine whether the high

methodsThe effect of LY3202626 versus vehicle on amyloid-β (Aβ) levels was evaluated in a series of

resultsLY3202626 exhibited significant human BACE1 inhibition, with an IC

conclusionLY3202626 is a potent BACE1 inhibitor with high blood-brain barrier permeability. The favorable safety and pharmacokinetic/pharmacodynamic profile of LY3202626 supports further clinical development.

Indexed as

Amyloid-βBACE1 inhibitorpharmacodynamicspharmacokineticstranslational studies

Identifiers

PMID35243208
PMCPMC8842743
OpenAlexW4206360148

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.