Evidence map›Paper›PMID 30742306›Full record

Trial reportJournal of clinical pharmacology2019

Population Pharmacokinetics of Vamorolone (VBP15) in Healthy Men and Boys With Duchenne Muscular Dystrophy.

Panteleimon D Mavroudis, John van den Anker, Laurie S Conklin, Jesse M Damsker, Eric P Hoffman, Kanneboyina Nagaraju, Paula R Clemens, William J Jusko

2 registry-linked trialsOpen access · greenAbstract readClinical Trial
In one paragraph

Trial report in Journal of clinical pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 30% 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.

NCT05166109 phase2completednot on this mapstarted 2022, after this paper: background citation

A Phase II Pilot Trial of Vamorolone vs. Placebo for the Treatment of Becker Muscular Dystrophy

TypeinterventionalSponsorReveraGen BioPharma, Inc.Ran2022 to 2025Enrolled46ConditionsBecker Muscular DystrophyArmsVamorolone, Placebo
NCT05185622 phase2completednot on this mapstarted 2022, after this paper: background citation

A Phase II Open-Label, Multiple Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Exploratory Efficacy of Vamorolone in Boys Ages 2 to <4 Years and 7 to <18 Years With Duchenne Muscular Dystrophy (DMD)

TypeinterventionalSponsorSanthera PharmaceuticalsRan2022 to 2024Enrolled54ConditionsDuchenne Muscular DystrophyArmsVamorolone
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
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  3. Article
  4. 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

8 authors at 5 institutions in 1 country.

Panteleimon D MavroudisDepartment of Pharmaceutical Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA.
John van den AnkerReveraGen Biopharma, Rockville, MD, USA.
Laurie S ConklinReveraGen Biopharma, Rockville, MD, USA.
Jesse M DamskerReveraGen Biopharma, Rockville, MD, USA.
Eric P HoffmanReveraGen Biopharma, Rockville, MD, USA.
Kanneboyina NagarajuReveraGen Biopharma, Rockville, MD, USA.
Paula R ClemensUniversity of Pittsburgh and Department of Veterans Affairs Medical Center, Pittsburgh, PA, USA.ORCID 0000-0002-0652-6703
William J JuskoDepartment of Pharmaceutical Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA.ORCID 0000-0003-4027-0550
Binghamton University · USChildren's National · USUniversity at Buffalo, State University of New York · USReveraGen BioPharma (United States) · USVA Pittsburgh Healthcare System · US

Funding

Corticosteroid Pharmacokinetics and PharmacodynamicsR37GM024211 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI JUSKO, WILLIAM J. · 2005 to 2014
$6.4M
Pivotal trial of vamorolone in Duchenne muscular dystrophyR44NS095423 · NINDS · REVERAGEN BIOPHARMA, INC. · PI CLEMENS, PAULA R, HOFFMAN, ERIC P. · 2016 to 2019
$6.1M
CORTICOSTEROID PHARMACOKINETICS/DYNAMICSR01GM024211 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI JUSKO, WILLIAM J. · 1985 to 2018
$4.7M
Dissociation of efficacy from side effects of anti-inflammatory therapies in Duchenne muscular dystrophyU54HD090254 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VAN DEN ANKER, JOHANNES NICOLAAS · 2016 to 2018
$2.5M
Dissociation of efficacy from side effects of anti-inflammatory therapies in Duchenne muscular dystrophyP50HD090254 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI CONKLIN, LAURIE S · 2019 to 2020
$1.6M
VBP15, an Innovative Steroid-like Intervention on DMD: VISION-DMDU34AR068616 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CLEMENS, PAULA R · 2015 to 2015
$300k
NIAMS NIH HHS U34 AR068616NICHD NIH HHS P50 HD090254NICHD NIH HHS U54 HD090254NIGMS NIH HHS R01 GM024211NIGMS NIH HHS R37 GM024211NINDS NIH HHS R44 NS095423
6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is an inherited neuromuscular disorder occurring in boys and caused by mutations in the dystrophin gene. Vamorolone is a first-generation delta-9,11 compound that has favorable efficacy and side effect profiles relative to classical glucocorticoids. The pharmacokinetics (PK) of oral vamorolone were assessed in parallel-group studies in healthy men (phase 1, n = 86) and boys with DMD (phase 2a, n = 48) during 14 days of once-daily dosing with a range of doses. Vamorolone exhibited moderate variability in PK, with the maximum plasma concentration usually occurring at 2-4 hours and a half-life of approximately 2 hours for all doses and days examined. Population PK modeling of all data together indicated that the PK of vamorolone can be well described by a 1-compartment model with zero-order absorption. Both men and boys showed a dose-linearity of PK parameters for the doses examined, with no accumulation of the drug during daily dosing. Ingestion with food resulted in markedly enhanced absorption of the drug, as tested in healthy men. There were similar PK of vamorolone in healthy men and DMD boys with apparent clearance averaging 2.0 L/h/kg in men and 1.7 L/h/kg in boys. Overall, vamorolone exhibited well-behaved linear PK, with similar profiles in healthy men and boys with DMD, moderate variability in PK parameters, and absorption and disposition profiles similar to those of classical glucocorticoids.

Indexed as

AdultAnti-Inflammatory AgentsArea Under CurveHumansMaleMiddle AgedMuscular Dystrophy, DuchennePregnadienediolsYoung AdultAnti-Inflammatory AgentsPregnadienediolsVBP15 compoundchildrenDuchenne muscular dystrophy (DMD)glucocorticoidsinflammationvamorolone

Identifiers

PMID30742306
PMCPMC6548694
OpenAlexW2914670333

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.