Eric Hoffman

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Associate Dean Research, Professor

Binghamton University School of Pharmacy and Pharmaceutical Sciences

United States

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Recent Grants

Grant: Close

Vamorolone trial in Becker muscular dystrophy

Open Date: 2021-09-15

Close Date: 2024-08-31

Grant: Close

Genetic Modifiers of Treatment Response in DMD

Open Date: 2020-10-01

Close Date: 2021-09-01

Grant: Close

Pilot Trial of Vamorolone for the Treatment of Becker Muscular Dystrophy

Open Date: 2020-07-13

Close Date: 2024-06-30

Grant: Close

Definition of pharmacodynamic biomarkers for juvenile dermatomyositis for clinical trials

Open Date: 2018-06-05

Close Date: 2019-11-30

Grant: Close

District of Columbia Intellectual and Developmental Disabilities Research Center

Open Date: 2016-09-22

Close Date: 2021-05-31

Articles (11)

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2024

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2020

Collaborators (6)

Eric Ortlund

Professor

Emory University School of Medicine

UNITED STATES

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Christopher Heier

Assistant Professor

George Washington University

UNITED STATES

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Utkarsh Dang

Assistant Professor

Carleton University

CANADA

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Alyson Fiorillo

Assistant Professor

Children's National Health System

UNITED STATES

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Xu Liu

Assistant Professor

Emory University

UNITED STATES

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Jason N. Berman

CANADA

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Eric Hoffman

Research Interests

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Recent Grants

Articles (11)

Return of participant-level clinical trial results to participants: pilot of a simplified centralised approach

A fleeting glimpse of functional benefit of the complete DMD gene in a large animal model of Duchenne muscular dystrophy

Loss of calpain3b in Zebrafish, a Model of Limb-Girdle Muscular Dystrophy, Increases Susceptibility to Muscle Defects Due to Elevated Muscle Activity

Muscle Weakness in Myositis: MicroRNA‐Mediated Dystrophin Reduction in a Myositis Mouse Model and Human Muscle Biopsies

Disruption of a key ligand-H-bond network drives dissociative properties in vamorolone for Duchenne muscular dystrophy treatment

Efficacy and safety of vamorolone in Duchenne muscular dystrophy: An 18-month interim analysis of a non-randomized open-label extension study

The discovery of dystrophin, the protein product of the Duchenne muscular dystrophy gene

A long-read RNA-seq approach to identify novel transcripts of very large genes

Serum biomarkers associated with baseline clinical severity in young steroid-naive Duchenne muscular dystrophy boys.

Pharmacotherapy of Duchenne Muscular Dystrophy.

Absolute quantification of dystrophin protein in human muscle biopsies using parallel reaction monitoring (PRM)

Collaborators (6)

Eric Ortlund

Christopher Heier

Utkarsh Dang

Alyson Fiorillo

Xu Liu

Jason N. Berman

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