Evidence map›Paper›PMID 40562976›Full record

ArticleThe AAPS journal2025

Pharmacokinetics and Pharmacodynamics of Nomlabofusp in Non-clinical Studies of Friedreich's Ataxia.

Flavia De Toni, Vanessa Ragaglia, Devin Schecter, Angela S Miller, Eric Gonzalez, Erik J Wagner, Xin Xu, R Mark Payne, Jean-Nicholas Mess, Matthew G Baile and 2 more

Abstract read
In one paragraph

Article in The AAPS journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Flavia De ToniLarimar Therapeutics Inc., Bala Cynwyd, PA, 3 Bala Plaza East, Suite 506, 19004, United States of America.ORCID 0000-0001-6701-7710
Vanessa RagagliaLarimar Therapeutics Inc., Bala Cynwyd, PA, 3 Bala Plaza East, Suite 506, 19004, United States of America.ORCID 0009-0007-3202-5447
Devin SchecterLarimar Therapeutics Inc., Bala Cynwyd, PA, 3 Bala Plaza East, Suite 506, 19004, United States of America.
Angela S MillerLarimar Therapeutics Inc., Bala Cynwyd, PA, 3 Bala Plaza East, Suite 506, 19004, United States of America.
Eric GonzalezNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, United States of America.
Erik J WagnerNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, United States of America.
Xin XuNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, United States of America.ORCID 0000-0003-1163-9304
R Mark PayneIndiana University School of Medicine, Indianapolis, IN, United States of America.ORCID 0000-0002-6232-3628
Jean-Nicholas MessAltasciences Inc., Montreal, QC, CA, Canada.ORCID 0009-0002-8756-3828
Matthew G BaileLarimar Therapeutics Inc., Bala Cynwyd, PA, 3 Bala Plaza East, Suite 506, 19004, United States of America.ORCID 0000-0002-2680-1178
Adrienne Clements-EganLarimar Therapeutics Inc., Bala Cynwyd, PA, 3 Bala Plaza East, Suite 506, 19004, United States of America.
Gopi ShankarLarimar Therapeutics Inc., Bala Cynwyd, PA, 3 Bala Plaza East, Suite 506, 19004, United States of America. gshankar@larimartx.com.ORCID 0009-0002-7224-1201

Funding

Pharmacokinetics and Drug MetabolismZIATR000369 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI XU, XIN · 2018 to 2025
$27.3M
Intramural NIH HHS ZIA TR000369
6 · The paper itself

Abstract

Nomlabofusp is a cell penetrant peptide-based recombinant fusion protein designed to enter cells and deliver human frataxin into the mitochondria of adults and children with Friedreich's ataxia. In this article we present non-clinical studies evaluating the pharmacology of nomlabofusp, including in a murine striated muscle tissue frataxin knockout model of Friedreich's ataxia. We demonstrate that subcutaneous administration of nomlabofusp distributes in a dose-dependent manner to several organs including the dorsal root ganglion, heart, and skeletal muscle, which are known to be predominantly affected in Friedreich's ataxia, as well as to other tissues, including skin. Plasma nomlabofusp concentrations correlated with levels of human frataxin delivered by nomlabofusp into tissues, and the increases in frataxin were correlated amongst tissues, especially with skin. In the knockout mice, we show that the pharmacokinetics and processing of nomlabofusp were comparable with wild type animals and that treatment with nomlabofusp halts the progression of cardiac dysfunction and significantly increased survival. Together, the findings from these non-clinical studies demonstrate that nomlabofusp exposure increases human frataxin in Friedreich's ataxia-relevant tissues and provide evidence of pharmacologic effects.

Indexed as

Friedreich AtaxiaIron-Binding ProteinsAnimalsDisease Models, AnimalDose-Response Relationship, DrugFrataxinHumansMaleMiceMice, KnockoutTissue DistributionFrataxinIron-Binding ProteinsAnimal modelFrataxinFriedreich’s ataxiaMitochondriaNomlabofuspNon-clinicalPharmacokinetics

Identifiers

PMID40562976
PMCPMC13143400

What OpenQuestion holds

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LicenceCC BY
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.