Evidence map›Paper›PMID 36920652›Full record

ReviewDrugs2023

A Review of RRx-001: A Late-Stage Multi-Indication Inhibitor of NLRP3 Activation and Chronic Inflammation.

Nanthini Jayabalan, Bryan Oronsky, Pedro Cabrales, Tony Reid, Scott Caroen, Aishwarya M Johnson, Natalia A Birch, John D O'Sullivan, Richard Gordon

Registry-linked trialOpen access · hybridFull text readReview
In one paragraph

Review in Drugs, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03699956 (A Phase 3, Controlled, Open-label, Randomized Study of RRx-001 Administered Sequentially With a Platinum Doublet or a Platinum Doublet in Third-Line or Beyond Small Cell Lung Cancer), which is not on this map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.5field-weighted citation impact, top 4% 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.

NCT03699956 phase3terminatednot on this map

A Phase 3, Controlled, Open-label, Randomized Study of RRx-001 Administered Sequentially With a Platinum Doublet or a Platinum Doublet in Third-Line or Beyond Small Cell Lung Cancer

TypeinterventionalSponsorEpicentRx, Inc.Ran2018 to 2024Enrolled18ConditionsCarcinoma, Small Cell LungArmsRRx-001 + eLOOP Device, Cisplatin/carboplatin plus etoposide
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. GSK461364 Inhibits NLRP3 Inflammasome by Targeting NEK7 Phosphorylation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. NLRP inflammasomes in health and disease.Molecular biomedicine · 2024
    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

9 authors at 5 institutions in 4 countries.

Nanthini JayabalanFaculty of Medicine, UQ Centre for Clinical Research (UQCCR), The University of Queensland, Brisbane, 4029, Australia.
Bryan OronskyEpicentRx, Torrey Pines, CA, 92307, USA. boronsky@epicentrx.com.
Pedro CabralesUCSD Department of Bioengineering, La Jolla, CA, 92093, USA.
Tony ReidEpicentRx, Torrey Pines, CA, 92307, USA.
Scott CaroenEpicentRx, Torrey Pines, CA, 92307, USA.
Aishwarya M JohnsonDepartment of Veterinary Medicine College of Food and Agriculture, Emirates University, Al Ain, UAE.
Natalia A BirchFaculty of Medicine, UQ Centre for Clinical Research (UQCCR), The University of Queensland, Brisbane, 4029, Australia.
John D O'SullivanFaculty of Medicine, UQ Centre for Clinical Research (UQCCR), The University of Queensland, Brisbane, 4029, Australia.
Richard GordonFaculty of Medicine, UQ Centre for Clinical Research (UQCCR), The University of Queensland, Brisbane, 4029, Australia. r.gordon1@uq.edu.au.ORCID http://orcid.org/0000-0003-2478-4607
The University of Queensland · AUTorrey Pines Institute For Molecular Studies · USLa Jolla Bioengineering Institute · USTranslational Research Institute · AUUnited Arab Emirates University · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic unresolving inflammation is emerging as a key underlying pathological feature of many if not most diseases ranging from autoimmune conditions to cardiometabolic and neurological disorders. Dysregulated immune and inflammasome activation is thought to be the central driver of unresolving inflammation, which in some ways provides a unified theory of disease pathology and progression. Inflammasomes are a group of large cytosolic protein complexes that, in response to infection- or stress-associated stimuli, oligomerize and assemble to generate a platform for driving inflammation. This occurs through proteolytic activation of caspase-1-mediated inflammatory responses, including cleavage and secretion of the proinflammatory cytokines interleukin (IL)-1β and IL-18, and initiation of pyroptosis, an inflammatory form of cell death. Several inflammasomes have been characterized. The most well-studied is the nucleotide-binding domain (NOD)-like receptor protein 3 (NLRP3) inflammasome, so named because the NLRP3 protein in the complex, which is primarily present in immune and inflammatory cells following activation by inflammatory stimuli, belongs to the family of nucleotide-binding and oligomerization domain (Nod) receptor proteins. Several NLRP3 inflammasome inhibitors are in development, all with multi-indication activity. This review discusses the current status, known mechanisms of action, and disease-modifying therapeutic potential of RRx-001, a direct NLRP3 inflammasome inhibitor under investigation in several late-stage anticancer clinical trials, including a phase 3 trial for the treatment of third-line and beyond small cell lung cancer (SCLC), an indication with no treatment, in which RRx-001 is combined with reintroduced chemotherapy from the first line, carboplatin/cisplatin and etoposide (ClinicalTrials.gov Identifier: NCT03699956). Studies from multiple independent groups have now confirmed that RRx-001 is safe and well tolerated in humans. Additionally, emerging evidence in preclinical animal models suggests that RRx-001 could be effective in a wide range of diseases where immune and inflammasome activation drives disease pathology.

Indexed as

InflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinAnimalsAzetidinesHumansInflammationNitro CompoundsNucleotidesAzetidinesInflammasomesNitro CompoundsNLR Family, Pyrin Domain-Containing 3 ProteinNucleotidesRRx-001

Identifiers

PMID36920652
PMCPMC10015535
OpenAlexW4324305882

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read20
identifiers read5
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.