Evidence map›Paper›PMID 32433779›Full record

ArticleJournal of clinical pharmacology2020

Predictors of Systemic Exposure to Topical Crisaborole: A Nonlinear Regression Analysis.

Vivek Purohit, Steve Riley, Huaming Tan, William C Ports

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-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.

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

5 citing papers in PubMed, 8 citations in OpenAlex.

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

4 authors at 1 institution in 1 country.

Vivek PurohitPfizer Inc, Groton, Connecticut, USA.
Steve RileyPfizer Inc, Groton, Connecticut, USA.
Huaming TanPfizer Inc, New York, New York, USA.
William C PortsPfizer Inc, Groton, Connecticut, USA.
Pfizer (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Crisaborole ointment, 2%, is a nonsteroidal phosphodiesterase 4 inhibitor for the treatment of mild to moderate atopic dermatitis. Results from 2 randomized, double-blind, vehicle-controlled phase 3 studies showed that twice-daily crisaborole in children and adults with mild to moderate atopic dermatitis was efficacious and well tolerated. Initial pharmacokinetics (PK) studies of crisaborole indicated absorption with measurable systemic levels of crisaborole. The current analysis was conducted to correlate steady-state systemic exposure parameters with ointment dose and identify covariates impacting PK parameters in healthy participants and patients with atopic dermatitis or psoriasis. A nonlinear regression analysis was conducted using ointment dose and noncompartmental PK parameters at steady state (area under the curve [AUC

Indexed as

Absorption, PhysiologicalAdministration, TopicalAdolescentAdultAgedArea Under CurveBoron CompoundsBridged Bicyclo Compounds, HeterocyclicChildChild, PreschoolClinical Trials, Phase I as TopicDermatitis, AtopicDermatologic AgentsDose-Response Relationship, DrugFemaleHealthy VolunteersBoron CompoundsBridged Bicyclo Compounds, HeterocycliccrisaboroleDermatologic AgentsOintmentsPhosphodiesterase 4 Inhibitorsarea under the curveatopic dermatitiscrisaborolemaximum concentrationpharmacokineticssteady state

Identifiers

PMID32433779
PMCPMC7540423
OpenAlexW3026917068

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.