Evidence map›Paper›PMID 32301501›Full record

Trial reportClinical pharmacology and therapeutics2020

Response to Inhibition of Receptor-Interacting Protein Kinase 1 (RIPK1) in Active Plaque Psoriasis: A Randomized Placebo-Controlled Study.

Kathleen Weisel, Scott Berger, Kim Papp, Catherine Maari, James G Krueger, Nicola Scott, Debra Tompson, Susanne Wang, Monica Simeoni, John Bertin and 1 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02776033 (A Multicentre, Randomised, Double-blind), which is not on this map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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.

NCT02776033 phase2completednot on this map

A Multicentre, Randomised, Double-blind (Sponsor-unblinded), Placebo-controlled, Repeat Dose Study to Investigate the Safety and Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of GSK2982772 in Subjects With Active Plaque-type Psoriasis

TypeinterventionalSponsorGlaxoSmithKlineRan2016 to 2018Enrolled65ConditionsPsoriasisArmsGSK2982772, Placebo
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
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  8. Mechanisms, regulation and clinical relevance of necroptosis.Nature reviews. Molecular cell biology · 2026
    Review
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  14. Programmed cell death of keratinocytes: an active driver in psoriasis.Apoptosis : an international journal on programmed cell death · 2026
    Review
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  16. PANoptosis: A novel therapeutic target in kidney disease (Review).International journal of molecular medicine · 2025
    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

11 authors at 6 institutions in 3 countries.

Kathleen WeiselGlaxoSmithKline, Collegeville, Pennsylvania, USA.
Scott BergerGlaxoSmithKline, Collegeville, Pennsylvania, USA.
Kim PappProbity Medical Research, Waterloo, Ontario, Canada.
Catherine MaariInnovaDerm Research, Montreal, Quebec, Canada.
James G KruegerThe Rockefeller University, New York, New York, USA.
Nicola ScottGlaxoSmithKline, Stevenage, UK.
Debra TompsonGlaxoSmithKline, Stevenage, UK.
Susanne WangGlaxoSmithKline, Collegeville, Pennsylvania, USA.
Monica SimeoniGlaxoSmithKline, Stockley Park, UK.
John BertinGlaxoSmithKline, Collegeville, Pennsylvania, USA.
Paul Peter TakGlaxoSmithKline, Stevenage, UK.
GlaxoSmithKline (United States) · USAge UK · GBGlaxoSmithKline (United Kingdom) · GBInnovaderm (Canada) · CAProbity Medical Research · CARockefeller University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Receptor-interacting protein kinase 1 (RIPK1), a regulator of inflammation and cell death, is a potential therapeutic target in immune-mediated inflammatory diseases (IMIDs). The objective of this phase IIa multicenter, randomized, double-blind, placebo-controlled study was to evaluate safety, tolerability pharmacokinetics, pharmacodynamics, and preliminary efficacy of GSK2982772, a RIPK1 inhibitor, in plaque-type psoriasis. Psoriasis patients (N = 65) were randomized to 60 mg twice daily (b.i.d.) or three times daily (t.i.d.), or placebo for 84 days. Most adverse events (AEs) were mild with no severe drug-related AEs reported. Plaque Lesion Severity Sum improved with b.i.d. treatment compared with placebo; interpretation of t.i.d. treatment results was complicated by a high placebo response. Reductions in epidermal thickness and infiltration by CD3+ T cells in the epidermis and dermis were observed compared with placebo. Results support the rationale for additional studies on RIPK1 inhibition in IMIDs.

Indexed as

AdultCanadaCD3 ComplexDermisDouble-Blind MethodFemaleHumansMaleMiddle AgedOxazepinesProtein Kinase InhibitorsPsoriasisReceptor-Interacting Protein Serine-Threonine KinasesRemission InductionSignal TransductionTime FactorsCD3 ComplexGSK2982772OxazepinesProtein Kinase InhibitorsReceptor-Interacting Protein Serine-Threonine KinasesRIPK1 protein, humanTriazoles

Identifiers

PMID32301501
PMCPMC7540322
OpenAlexW3016766421

What OpenQuestion 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 OpenQuestion graph.