Evidence map›Paper›PMID 38655895›Full record

Trial reportPharmacology research & perspectives2024

Clinical pharmacology and tolerability of REC-994, a redox-cycling nitroxide compound, in randomized phase 1 dose-finding studies.

Ron Alfa, Timothy Considine, Shafique Virani, Matt Pfeiffer, Anthony Donato, Daniel Dickerson, Diana Shuster, Joel Ellis, Kristen Rushton, Helen Wei and 1 more

Open access · goldAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Pharmacology research & perspectives, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
9.3field-weighted citation impact, top 2% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
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  5. 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 3 institutions in 1 country.

Ron AlfaRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.
Timothy ConsidineRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.
Shafique ViraniRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.
Matt PfeifferRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.
Anthony DonatoDepartment of Internal Medicine, University of Utah, Salt Lake City, Utah, USA.
Daniel DickersonICONplc (Legacy PRA Health Sciences), Lenexa, Kansas, USA.
Diana ShusterRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.ORCID https://orcid.org/0000-0003-0353-5900
Joel EllisRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.
Kristen RushtonRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.
Helen WeiRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.
Christopher GibsonRecursion Pharmaceuticals, Inc., Salt Lake City, Utah, USA.ORCID https://orcid.org/0009-0000-1052-9723
Arrien Pharmaceuticals (United States) · USPRA Health Sciences · USUniversity of Utah · US

Funding

IMPACT OF T CELLS ON AGE-RELATED VASCULAR DYSFUNCTION: A TRANSLATIONAL APPROACH - DIVERSITY SUPPLEMENTR01AG060395 · NIA · UNIVERSITY OF UTAH · PI DONATO, ANTHONY JOHN · 2019 to 2023
$2.5M
Integrative Mechanisms of Vascular AgingR01AG077751 · NIA · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Anthony John Donato, Lisa A Lesniewski · 2023 to 2026
$1.8M
Improving healthspan through discovery of potent NAMPT activators from a DNA-encoded libraryR21AG074498 · NIA · UNIVERSITY OF UTAH · PI DONATO, ANTHONY JOHN, FRANZINI, RAPHAEL M. · 2022 to 2023
$436k
Targeting Cardiovascular Disease with SIRT6 ActivatorsR21AG070740 · NIA · UNIVERSITY OF UTAH · PI FRANZINI, RAPHAEL M. · 2021 to 2022
$433k
CSRD VA I01 CX002211NIA NIH HHS R01 AG060395NIA NIH HHS R01 AG077751NIA NIH HHS R21 AG070740NIA NIH HHS R21 AG074498Recursion Pharmaceuticals, Inc.
6 · The paper itself

Abstract

Cerebral cavernous malformation (CCM) has variable clinical symptoms, including potentially fatal hemorrhagic stroke. Treatment options are very limited, presenting a large unmet need. REC-994 (also known as tempol), identified as a potential treatment through an unbiased drug discovery platform, is hypothesized to treat CCMs through a reduction in superoxide, a reactive oxygen species. We investigated the safety, tolerability, and pharmacokinetic profile of REC-994 in healthy volunteers. Single- and multiple-ascending dose (SAD and MAD, respectively) studies were conducted in adult volunteers (ages 18-55). SAD study participants received an oral dose of REC-994 or placebo. MAD study participants were randomized 3:1 to oral doses of REC-994 or matching placebo, once daily for 10 days. Thirty-two healthy volunteers participated in the SAD study and 52 in the MAD study. Systemic exposure increased in proportion to REC-994 dose after single doses of 50-800 mg and after 10 days of dosing over the 16-fold dose range of 50-800 mg. Median T

Indexed as

Cyclic N-OxidesDose-Response Relationship, DrugSpin LabelsAdministration, OralAdolescentAdultDouble-Blind MethodFemaleHealthy VolunteersHemangioma, Cavernous, Central Nervous SystemHumansMaleMiddle AgedOxidation-ReductionYoung AdultCyclic N-OxidesSpin Labelstempolantioxidantsgenetic diseasesoxidative stresspharmacokineticsphase 1

Identifiers

PMID38655895
PMCPMC11040693
OpenAlexW4395074029

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.