Evidence map›Paper›PMID 32250021›Full record

Trial reportClinical pharmacology in drug development2020

A Single-Dose, Open-Label, Randomized, Two-Way Crossover Study in Healthy Japanese Participants to Evaluate the Bioequivalence and the Food Effect on the Pharmacokinetics of Daprodustat.

Masanori Yamada, Minori Osamura, Hirofumi Ogura, Tomohiro Onoue, Akira Wakamatsu, Yotaro Numachi, Stephen Caltabiano, Kelly M Mahar

Registry-linked trialOpen access · hybridAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology in drug development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03493386 (A Single Centre, Single Dose, Open-label, Randomised, 2-way Crossover Study in Healthy Japanese Male Subjects to Evaluate the Bioequivalence of Daprodustat Tablets), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 50% 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.

NCT03493386 phase1completednot on this map

A Single Centre, Single Dose, Open-label, Randomised, 2-way Crossover Study in Healthy Japanese Male Subjects to Evaluate the Bioequivalence of Daprodustat Tablets (2 mg Tablet vs. 4 mg Tablet) (Part 1) and the Food Effect on the Pharmacokinetics of Daprodustat (Part 2)

TypeinterventionalSponsorGlaxoSmithKlineRan2018 to 2018Enrolled64ConditionsAnaemiaArmsDaprodustat 2 mg tablet, Daprodustat 4 mg tablet
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

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

8 authors at 2 institutions in 2 countries.

Masanori YamadaClinical Pharmacology Office, Japan Development Division, GlaxoSmithKline K.K., Tokyo, Japan.
Minori OsamuraClinical Pharmacology Office, Japan Development Division, GlaxoSmithKline K.K., Tokyo, Japan.
Hirofumi OguraClinical Pharmacology Office, Japan Development Division, GlaxoSmithKline K.K., Tokyo, Japan.
Tomohiro OnoueBiomedical Data Sciences Department, Japan Development Division, GlaxoSmithKline K.K., Tokyo, Japan.
Akira WakamatsuPre-Clinical Development Department, Japan Development Division, GlaxoSmithKline K.K., Tokyo, Japan.
Yotaro NumachiMedicines Development, Japan Development Division, GlaxoSmithKline K.K., Tokyo, Japan.
Stephen CaltabianoClinical Development, GlaxoSmithKline, Collegeville, Pennsylvania, USA.
Kelly M MaharClinical Pharmacology, Modeling and Simulation, GlaxoSmithKline, Collegeville, Pennsylvania, USA.
GlaxoSmithKline (Japan) · JPGlaxoSmithKline (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Daprodustat is a prolyl hydroxylase inhibitor that stimulates erythropoiesis in a manner similar to the natural response to hypoxia, whereby inhibition of hypoxia inducible factor (HIF) prolyl-4-hydroxylases by daprodustat ultimately results in increased levels of HIF-responsive genes. Daprodustat is under development as an emerging new class of agents for the treatment of anemia associated with chronic kidney disease (CKD). This was a single-center, single-dose, open-label, randomized, 2-way crossover study in healthy Japanese male participants consisting of 2 parts. The primary objective was to evaluate the bioequivalence (BE) between daprodustat tablet strengths (part 1) and to evaluate the food effect on the pharmacokinetics (PK) of daprodustat (part 2). A total of 64 healthy Japanese male participants were enrolled; 52 participants were included in part 1 and 12 in part 2. BE was demonstrated between the daprodustat 2-mg tablet and the daprodustat 4-mg tablet. A standard CKD meal did not have a large effect on the PK parameters of daprodustat after a single oral dose of daprodustat 4 mg. Administration of single oral doses of daprodustat 4 mg was generally well tolerated in the healthy Japanese participants, and no new safety signals were identified without regard to food.

Indexed as

Therapeutic EquivalencyAdministration, OralAdultAnemiaArea Under CurveAsian PeopleBarbituratesCross-Over StudiesDose-Response Relationship, DrugDrug Administration ScheduleErythropoiesisFood-Drug InteractionsGlycineHealthy VolunteersHumansMaleBarbituratesGlycineGSK1278863Pharmaceutical PreparationsProlyl-Hydroxylase Inhibitorsbioequivalencedaprodustatfood effecthealthy subjectJapanesepharmacokineticssafetysingle dose

Identifiers

PMID32250021
PMCPMC7687240
OpenAlexW3014691755

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.