Evidence map›Paper›PMID 30012772›Full record

ArticleAntimicrobial agents and chemotherapy2018

Extended-Duration MK-8591-Eluting Implant as a Candidate for HIV Treatment and Prevention.

Stephanie E Barrett, Ryan S Teller, Seth P Forster, Li Li, Megan A Mackey, Daniel Skomski, Zhen Yang, Kerry L Fillgrove, Gregory J Doto, Sandra L Wood and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

61 citing papers in PubMed, 130 citations in OpenAlex.

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  11. Antiviral potency of long-acting islatravir subdermal implant in SHIV-infected macaques.Journal of controlled release : official journal of the Controlled Release Society · 2024
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1 more citing papers are in PubMed but not listed here.

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

18 authors at 2 institutions in 1 country.

Stephanie E BarrettPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA Stephanie_barrett@merck.com.ORCID 0000-0002-9681-1750
Ryan S TellerPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
Seth P ForsterPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
Li LiPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
Megan A MackeyPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
Daniel SkomskiPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
Zhen YangPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
Kerry L FillgrovePharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck & Co., Inc., West Point, Pennsylvania, USA.
Gregory J DotoSafety Assessment and Laboratory Animals Research, Merck & Co., Inc., West Point, Pennsylvania, USA.
Sandra L WoodSafety Assessment and Laboratory Animals Research, Merck & Co., Inc., West Point, Pennsylvania, USA.
Jose LebronSafety Assessment and Laboratory Animals Research, Merck & Co., Inc., West Point, Pennsylvania, USA.
Jay A GroblerInfectious Diseases Discovery Research, Merck & Co., Inc., West Point, Pennsylvania, USA.
Rosa I SanchezPharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck & Co., Inc., West Point, Pennsylvania, USA.
Zhen LiuPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
Bing LuPharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck & Co., Inc., West Point, Pennsylvania, USA.
Tao NiuPharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck & Co., Inc., West Point, Pennsylvania, USA.
Li SunPharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck & Co., Inc., West Point, Pennsylvania, USA.
Marian E GindyPharmaceutical Sciences, Merck & Co., Inc., West Point, Pennsylvania, USA.
United States Military Academy · USMerck & Co., Inc., Rahway, NJ, USA (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regimen adherence remains a major hurdle to the success of daily oral drug regimens for the treatment and prevention of human immunodeficiency virus (HIV) infection. Long-acting drug formulations requiring less-frequent dosing offer an opportunity to improve adherence and allow for more forgiving options with regard to missed doses. The administration of long-acting formulations in a clinical setting enables health care providers to directly track adherence. MK-8591 (4'-ethynyl-2-fluoro-2'-deoxyadenosine [EFdA]) is an investigational nucleoside reverse transcriptase translocation inhibitor (NRTTI) drug candidate under investigation as part of a regimen for HIV treatment, with potential utility as a single agent for preexposure prophylaxis (PrEP). The active triphosphate of MK-8591 (MK-8591-TP) exhibits protracted intracellular persistence and, together with the potency of MK-8591, supports its consideration for extended-duration dosing. Toward this end, drug-eluting implant devices were designed to provide prolonged MK-8591 release

Indexed as

AnimalsAnti-HIV AgentsDeoxyadenosinesDrug CarriersHIV-1HIV InfectionsMacaca mulattaMalePolymersRatsRats, WistarReverse Transcriptase InhibitorsAnti-HIV AgentsDeoxyadenosinesDrug CarriersislatravirPolymersReverse Transcriptase Inhibitorsextended durationHIV preventionHIV treatmenthuman immunodeficiency viruslong-acting implant

Identifiers

PMID30012772
PMCPMC6153840
OpenAlexW2883638714

What OpenQuestion holds

Textmetadata
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.