Evidence map›Paper›PMID 32556602›Full record

Trial reportCancer chemotherapy and pharmacology2020

Effect of food on the pharmacokinetics of the WEE1 inhibitor adavosertib (AZD1775) in patients with advanced solid tumors.

Mats Någård, Mei-Lin Ah-See, Karen So, Marit Vermunt, Fiona Thistlethwaite, Mariette Labots, Patricia Roxburgh, Alain Ravaud, Mario Campone, Liselot Valkenburg-van Iersel and 3 more

Open access · hybridAbstract readClinical Trial, Phase IMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Cancer chemotherapy and pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-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.

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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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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

13 authors at 10 institutions in 5 countries.

Mats NågårdClinical Pharmacology and Quantitative Pharmacology, R&D Clinical Pharmacology and Safety Sciences, AstraZeneca, Gaithersburg, MD, USA.
Mei-Lin Ah-SeeLate Stage Development, Oncology R&D, AstraZeneca, Cambridge, UK.
Karen SoLate Stage Development, Oncology R&D, AstraZeneca, Cambridge, UK.
Marit VermuntThe Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Fiona ThistlethwaiteThe Christie NHS Foundation Trust and University of Manchester, Manchester, UK.
Mariette LabotsCancer Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.
Patricia RoxburghBeaston West of Scotland Cancer Centre and University of Glasgow, Glasgow, UK.
Alain RavaudBordeaux University Hospital, Bordeaux, France.
Mario CamponeICO - Site René, Saint Herblain, France.
Liselot Valkenburg-van IerselMaastricht University Medical Centre, Maastricht, The Netherlands.
Lone OttesenLate Stage Development, Oncology R&D, AstraZeneca, Cambridge, UK.
Yan LiClinical Pharmacology Biologics and Bioanalysis, Clinical Pharmacology and Safety Science, BioPharmaceuticals R&D, AstraZeneca, Boston, MA, USA.
Ganesh MugunduClinical Pharmacology and Quantitative Pharmacology, R&D Clinical Pharmacology and Safety Sciences, AstraZeneca, 35 Gatehouse Drive, Waltham, MA, 02451, USA. ganesh.mugundu@astrazeneca.com.ORCID http://orcid.org/0000-0002-3736-1884
AstraZeneca (United Kingdom) · GBAstraZeneca (United States) · USAmsterdam University Medical Centers · NLAstraZeneca (South Korea) · KRBeatson West of Scotland Cancer Centre · GBBordeaux Population Health · FRInstitut Génétique Nantes Atlantique · FRMaastricht University Medical Centre · NLThe Netherlands Cancer Institute · NLUniversity of Manchester · GB

Funding

Cancer Research UKDepartment of Health
6 · The paper itself

Abstract

purposeTo support future dosing recommendations, the effect of food on the pharmacokinetics of adavosertib, a first-in-class, small-molecule reversible inhibitor of WEE1 kinase, was assessed in patients with advanced solid tumors.

methodsIn this Phase I, open-label, randomized, two-period, two-sequence crossover study, the pharmacokinetics of a single 300 mg adavosertib dose were investigated in fed versus fasted states.

resultsCompared with the fasted state, a high-fat, high-calorie meal (fed state) decreased adavosertib maximum plasma concentration (C

conclusionA high-fat meal did not have a clinically relevant effect on the systemic exposure of adavosertib, suggesting that adavosertib can be administered without regard to meals.

Indexed as

Food-Drug InteractionsAdministration, OralAdultAgedAntineoplastic AgentsBiological AvailabilityCell Cycle ProteinsCross-Over StudiesDiet, High-FatFemaleHumansMaleMiddle AgedNeoplasmsProtein Kinase InhibitorsProtein-Tyrosine KinasesadavosertibAntineoplastic AgentsCell Cycle ProteinsProtein Kinase InhibitorsProtein-Tyrosine KinasesPyrazolesPyrimidinonesWEE1 protein, humanAdavosertibFood effectOncologyPharmacokineticsWEE1

Identifiers

PMID32556602
PMCPMC7338825
OpenAlexW3036679145

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.