Evidence map›Paper›PMID 27245340›Full record

Trial reportEuropean journal of drug metabolism and pharmacokinetics2017

Assessment of Drug-Drug Interaction Potential Between Atorvastatin and LCZ696, A Novel Angiotensin Receptor Neprilysin Inhibitor, in Healthy Chinese Male Subjects.

Surya Ayalasomayajula, Wei Pan, Yi Han, Fan Yang, Thomas Langenickel, Parasar Pal, Wei Zhou, Yaozong Yuan, Iris Rajman, Gangadhar Sunkara

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in European journal of drug metabolism and pharmacokinetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

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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

10 authors at 5 institutions in 3 countries.

Surya AyalasomayajulaDrug Metabolism and Pharmacokinetics, Novartis Institutes for BioMedical Research, East Hanover, NJ, USA. surya.ayalasomayajula@novartis.com.
Wei PanDrug Metabolism and Pharmacokinetics, Novartis Institutes for BioMedical Research, Shanghai, China.
Yi HanDrug Metabolism and Pharmacokinetics, Novartis Institutes for BioMedical Research, Shanghai, China.
Fan YangClinical Sciences and Innovation, Novartis Institutes for Biomedical Research, Shanghai, China.
Thomas LangenickelTranslational Medicine, Clinical Pharmacology and Profiling, Novartis Institutes for Biomedical Research, Basel, Switzerland.
Parasar PalBiostatistical Sciences, Novartis Healthcare Private Limited, Hyderabad, India.
Wei ZhouDrug Metabolism and Pharmacokinetics, Novartis Institutes for BioMedical Research, East Hanover, NJ, USA.
Yaozong YuanDepartment of Gastroenterology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Iris RajmanTranslational Medicine, Clinical Pharmacology and Profiling, Novartis Institutes for Biomedical Research, Basel, Switzerland.
Gangadhar SunkaraDrug Metabolism and Pharmacokinetics, Novartis Institutes for BioMedical Research, East Hanover, NJ, USA.
Novartis (China) · CNNovartis (India) · INNovartis Institutes for BioMedical ResearchNovartis (Switzerland) · CHRuijin Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveLCZ696 (sacubitril/valsartan), a novel angiotensin receptor neprilysin inhibitor has been recently approved for the treatment of patients with heart failure (HF) and reduced ejection fraction. As several HF patients are likely to use statins as co-medications, the potential for a pharmacokinetic drug-drug interaction between atorvastatin and LCZ696 was evaluated.

methodsThis was an open-label, three-period, single-sequence study in 28 healthy Chinese male subjects wherein LCZ696 200 mg was administered twice daily for 5 days in period 1. Following a washout period, atorvastatin 80 mg was administered once daily for 4 days (period 2) and subsequently co-administered with LCZ696 200 mg for 5 days (period 3). Serial plasma samples were collected to determine pharmacokinetic parameters of LCZ696 analytes (sacubitril, LBQ657, and valsartan) and atorvastatin and its metabolites.

resultsAtorvastatin co-administration had no effect on the pharmacokinetics of LBQ657, while the AUC

conclusionsWhile atorvastatin had no significant impact on the pharmacokinetics of LCZ696 analytes upon co-administration, the C

Indexed as

AdultAminobutyratesAngiotensin Receptor AntagonistsAnticholesteremic AgentsArea Under CurveAsian PeopleAtorvastatinBiphenyl CompoundsChinaDrug CombinationsDrug InteractionsHumansMaleNeprilysinTetrazolesValsartanAminobutyratesAngiotensin Receptor AntagonistsAnticholesteremic AgentsAtorvastatinBiphenyl CompoundsDrug CombinationsNeprilysinsacubitril and valsartan sodium hydrate drug combinationTetrazolesValsartan

Identifiers

PMID27245340
OpenAlexW2415731917

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.