Evidence map›Paper›PMID 29799676›Full record

Trial reportClinical pharmacology in drug development2019

Pharmacokinetic Study of Rucaparib in Patients With Advanced Solid Tumors.

Geoffrey I Shapiro, Rebecca S Kristeleit, Howard A Burris, Patricia LoRusso, Manish R Patel, Yvette Drew, Heidi Giordano, Lara Maloney, Simon Watkins, Sandra Goble and 2 more

Registry-linked trialAbstract readClinical Trial, Phase IClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology in drug development, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01482715 (A Phase I/II, Open-Label, Safety, Pharmacokinetic, and Preliminary Efficacy Study of Oral Rucaparib in Patients With gBRCA Mutation Ovarian Cancer or Other Solid Tumor), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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.

NCT01482715 phase1 / phase2completednot on this map

A Phase I/II, Open-Label, Safety, Pharmacokinetic, and Preliminary Efficacy Study of Oral Rucaparib in Patients With gBRCA Mutation Ovarian Cancer or Other Solid Tumor

TypeinterventionalSponsorpharmaand GmbHRan2011 to 2019Enrolled136ConditionsOvarian Cancer, Fallopian Tube Cancer, Peritoneal Cancer, Advanced Solid Tumor With Evidence of Germline or Somatic BRCAArmsRucaparib
3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Trial
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  5. Review
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  8. Recent advances in pharmaceutical cocrystals of theophylline.Natural products and bioprospecting · 2024
    Review
  9. Article
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  11. Review
  12. Review
  13. Article
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  15. Article
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  17. Review
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  20. 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

12 authors.

Geoffrey I ShapiroDana-Farber Cancer Institute, Boston, MA, USA.
Rebecca S KristeleitUCL Cancer Institute, London, United Kingdom.
Howard A BurrisSarah Cannon Research Institute at Tennessee Oncology, Nashville, TN, USA.
Patricia LoRussoYale University, New Haven, CT, USA.
Manish R PatelSarah Cannon Research Institute at Florida Cancer Specialists, Sarasota, FL, USA.
Yvette DrewNorthern Centre for Cancer Care, Newcastle upon Tyne, United Kingdom.
Heidi GiordanoClovis Oncology, Inc., Boulder, CO, USA.
Lara MaloneyClovis Oncology, Inc., Boulder, CO, USA.
Simon WatkinsClovis Oncology, Inc., Boulder, CO, USA.
Sandra GobleClovis Oncology, Inc., Boulder, CO, USA.
Sarah Jaw-TsaiClovis Oncology, Inc., Boulder, CO, USA.
Jim J XiaoClovis Oncology, Inc., Boulder, CO, USA.

Funding

Department of HealthWellcome Trust
6 · The paper itself

Abstract

The phase 1-2 study CO-338-010 (Study 10; NCT01482715) is evaluating single-agent rucaparib, a poly(ADP-ribose) polymerase inhibitor, administered orally to patients with an advanced solid tumor. In the dose escalation phase (Part 1), we characterized the single-dose and steady-state pharmacokinetic profiles of rucaparib administered once daily (QD; dose range, 40-500 mg; n = 16) or twice daily (BID; dose range, 240-840 mg; n = 30). Across all dosing schedules examined, the plasma exposure of rucaparib was approximately dose proportional; half-life was approximately 17 hours, and median time to maximum concentration (t

Indexed as

Food-Drug InteractionsAdministration, OralAdultAgedAntineoplastic AgentsDrug Administration ScheduleFastingFemaleHumansIndolesMaleMiddle AgedNeoplasmsPoly(ADP-ribose) Polymerase InhibitorsYoung AdultAntineoplastic AgentsIndolesPoly(ADP-ribose) Polymerase Inhibitorsrucaparibfood effectPARP inhibitionpharmacokineticsrucaparibtablet

Identifiers

PMID29799676
PMCPMC6585632

What OpenQuestion holds

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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.