Evidence map›Paper›PMID 28727908›Full record

Trial reportClinical and translational science2017

Leveraging a Clinical Phase Ib Proof-of-Concept Study for the GPR40 Agonist MK-8666 in Patients With Type 2 Diabetes for Model-Informed Phase II Dose Selection.

A W Krug, P Vaddady, R A Railkar, B J Musser, J Cote, Agh Ederveen, D G Krefetz, E DeNoia, A L Free, L Morrow and 4 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical and translational science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01971554 (A Multiple Dose Clinical Trial to Study the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of MK-8666 in Type 2 Diabetes Mellitus Patients), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 31% 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.

NCT01971554 phase1completednot on this map

A Multiple Dose Clinical Trial to Study the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of MK-8666 in Type 2 Diabetes Mellitus Patients

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2013 to 2014Enrolled63ConditionsType 2 Diabetes MellitusArmsMK-8666, Placebo
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Pharmacology of Free Fatty Acid Receptors and Their Allosteric Modulators.International journal of molecular sciences · 2021
    Review
  7. Article
  8. 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

14 authors at 7 institutions in 2 countries.

A W KrugMerck & Co., Inc., Kenilworth, New Jersesy, USA.
P VaddadyMerck & Co., Inc., Kenilworth, New Jersesy, USA.
R A RailkarMerck & Co., Inc., Kenilworth, New Jersesy, USA.
B J MusserMerck & Co., Inc., Kenilworth, New Jersesy, USA.
J CoteMerck & Co., Inc., Kenilworth, New Jersesy, USA.
Agh EderveenCBG-MEB, Utrecht, The Netherlands.
D G KrefetzPRA Health Sciences, Marlton, New Jersey, USA.
E DeNoiaICON Development Solutions, San Antonio, Texas, USA.
A L FreePinnacle Research Group, Anniston, Alabama, USA.
L MorrowProfil Institute for Clinical Research, Chula Vista, California, USA.
M V ChakravarthyMerck & Co., Inc., Kenilworth, New Jersesy, USA.
E KauhMerck & Co., Inc., Kenilworth, New Jersesy, USA.
D A TatosianMerck & Co., Inc., Kenilworth, New Jersesy, USA.
P A KothareMerck & Co., Inc., Kenilworth, New Jersesy, USA.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USEli Lilly (United States) · USMedicines Evaluation Board · NLPinnacle Clinical Research · USPRA Health Sciences · USPrecision Research Institute · USThe University of Texas at San Antonio · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GPR40 mediates free fatty acid-induced insulin secretion in beta cells. We investigated the safety, pharmacokinetics, and glucose response of MK-8666, a partial GPR40 agonist, after once-daily multiple dosing in type 2 diabetes patients. This double-blind, multisite, parallel-group study randomized 63 patients (placebo, n = 18; 50 mg, n = 9; 150 mg, n = 18; 500 mg, n = 18) for 14-day treatment. The results showed no serious adverse effects or treatment-related hypoglycemia. One patient (150-mg group) showed mild-to-moderate transaminitis at the end of dosing. Median MK-8666 T

Indexed as

AdultAgedBlood GlucoseDiabetes Mellitus, Type 2Dose-Response Relationship, DrugEndpoint DeterminationHumansLeast-Squares AnalysisMiddle AgedModels, BiologicalProof of Concept StudyReceptors, G-Protein-CoupledTreatment OutcomeBlood GlucoseFFAR1 protein, humanReceptors, G-Protein-Coupled

Identifiers

PMID28727908
PMCPMC5593169
OpenAlexW2738817021

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.