Evidence map›Paper›PMID 32166864›Full record

Trial reportClinical and translational science2020

Effect of Rifampin-Mediated OATP1B1 and OATP1B3 Transporter Inhibition on the Pharmacokinetics of the P2Y12 Receptor Antagonist Selatogrel.

Uta Schilling, Jasper Dingemanse, Christine Voors-Pette, Christel Romeijn, Peter Dogterom, Mike Ufer

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

Trial report in Clinical and translational science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03814200 (A Single-center, Randomized, Double-blind, Two-period Cross-over Study to Investigate the Effect of a Single Intravenous Dose of Rifampicin on the Pharmacokinetics of ACT-246475 in Healthy Subjects), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% 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.

NCT03814200 phase1completednot on this map

A Single-center, Randomized, Double-blind, Two-period Cross-over Study to Investigate the Effect of a Single Intravenous Dose of Rifampicin on the Pharmacokinetics of ACT-246475 in Healthy Subjects

TypeinterventionalSponsorViatris Innovation GmbHRan2019 to 2019Enrolled14ConditionsHealthy SubjectArmsSaline, ACT-246475, Rifampicin
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
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

6 authors at 2 institutions in 2 countries.

Uta SchillingDepartment of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd., Allschwil, Switzerland.
Jasper DingemanseDepartment of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd., Allschwil, Switzerland.
Christine Voors-PetteQPS Netherlands B.V., Groningen, The Netherlands.
Christel RomeijnQPS Netherlands B.V., Groningen, The Netherlands.
Peter DogteromQPS Netherlands B.V., Groningen, The Netherlands.
Mike UferDepartment of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd., Allschwil, Switzerland.
Idorsia (Switzerland) · CHQPS (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In vitro studies have indicated that the P2Y12 receptor antagonist selatogrel is a substrate of organic anion-transporting-polypeptide (OATP)1B1 and OATP1B3 that are known to mediate hepatic uptake. Selatogrel is primarily eliminated via the biliary route. Therefore, the study aim was to investigate the effect of rifampin-mediated OATP1B1 and OATP1B3 inhibition on the pharmacokinetics (PK) of selatogrel. This was a randomized, double-blind, placebo-controlled, two-period, crossover study in 14 healthy subjects. In each period, a single subcutaneous dose of 4 mg selatogrel was administered, either immediately after a single intravenous 30 minutes infusion of 600 mg rifampin or after placebo. Plasma samples were collected for 36 hours and analyzed using a validated liquid chromatography-tandem mass spectrometry method. PK parameters of selatogrel were calculated using noncompartmental analysis. The effect of rifampin was explored based on geometric mean peak plasma concentration (C

Indexed as

AdolescentAdultAgedCross-Over StudiesDouble-Blind MethodDrug Administration ScheduleDrug InteractionsFemaleHalf-LifeHealthy VolunteersHumansLiver-Specific Organic Anion Transporter 1MaleMiddle AgedOrganophosphonatesPurinergic P2Y Receptor AntagonistsLiver-Specific Organic Anion Transporter 1OrganophosphonatesP2RY12 protein, humanPurinergic P2Y Receptor AntagonistsPyrimidinesReceptors, Purinergic P2Y12RifampinselatogrelSLCO1B1 protein, humanSLCO1B3 protein, humanSolute Carrier Organic Anion Transporter Family Member 1B3

Identifiers

PMID32166864
PMCPMC7485944
OpenAlexW3011161555

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.