
Christopher E Hopkins, PhD, MBA

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About me
CEO at Glafabra Therapeutics / Genetically-Engineered Cell Therapies / Founder of Devinebio
Education

University of Utah
1986 - 1991BS BiologyAtividades e grupos:Worked on conotoxin neurotoxin isolation and characterization

Westminster College
2010 - 2012Master of Business Administration (MBA) Project-based degreeProject-based MBA at Westminster allowed advancement of startup company (Knudra Transgenics) by directly applying curriculum to company growth needs. Hands-on approach was vital to orienting the company to successful exit.

Boston University
1997 - 2003Ph. D. Biochemistry and Molecular BiologyPerformed biochemical and molecular interrogation of aldolase 1,6 bisphospate aldolase
Experience

University of Utah
Jan 1987 - Jan 1996Chris worked in Dr Raymond Gesteland lab to develop ESI mass spec polymorphism analysis Chris worked with Dr. Tom Alber to perform studies on circularly permuted lysozyme. In Dr. Toto Olivera lab at U of Utah, Chris invented snail milking technique used to isolation of conotoxin neuropeptides.
Research Associate
Jan 1992 - Jan 1996Research Technician
Jan 1991 - Jan 1992Research Technician
Jan 1987 - Jan 1991

Hybridon, Inc
Jan 1996 - Jan 1997Research AssociateChris worked with Dr. Bing Wang to developed novel oligonucleotide sequencing methodology at antisense therapeutics company

Boston University
Jan 1997 - Jan 2002Graduate degreeIn Dr Dean Tolan Lab, Chris combined Mass Spec, NMR, and X-ray studies with chemical modification rescue experiments to dissect molecular mechanism of Aldolase function.

University of Utah
Jan 2003 - Jan 2010Post DocorateChris worked with Dr Erik Jorgensen and Dr Christan Frokjaer-Jensen in the development MosSCI transgenesis technology.

Knudra Transgenics
Jan 2009 - Jan 2017Founder and Chief Science OfficerKnudra Transgenics provided Genomes Built to Spec which created customized transgenics in C. elegans and zebrafish. As founder, Chris harnessed a passion for advancing medical discovery into a first-in-kind service for the C. elegans and zebrafish research community. Chris helped pioneer the adoption of CRISPR-editing into multiple research lab workflows. Knudra Transgenics was acquired by NemaMetrix (now InVivo Biosystems) in late 2017. Chris retained his role as CSO.

AxumBio
Mar 2012 - Jul 2017FounderAxumbio developed discovery platforms for finding novel anti-parasite drugs. Chris pioneered the use of genome engineering techniques create new discovery systems expressing specific parasite genes.

InVivo Biosystems
Jan 2017 - Jan 2024Chief Science OfficerIn Vivo Biosystems is a platform drug discovery company with an innovative pipeline in CNS, metabolic, cardio and cancer portfolios. In the role as Chief Science Officer, Chris facilitates market adoption of these proprietary systems into pharma, biotech and related industries. The role includes new product innovation, market outreach, business development, and strategic planning.

Devinebio
Jan 2020 - nowFounderDevinebio partners with emerging foundations and companies in the biotech space to find genetic medicines to develop as treatment for their rare disease. We help Patient Advocacy Groups (PAGs) and new biotechs develop strategies that get them from target to IND enabled, which is often a key value inflection that gets the attention of big Pharma. We first focus on drug repurposing and then biologics (ASO and AAV) as the fastest route to getting these needed treatments into the marketplace.

CureCADASIL
Jan 2022 - nowSAB memberAs a member of the SAB at cureCADASIL, Chris used his experience in entrepreneurship in biochemistry and genetics to help found the CADASIL Disease Modeling Group (CDMG). The group brings together leading vascular biology researchers with the bold 5 step mission: 1) Create a USA-based aggregate patient registry within 1 year, 2) Deploy omics technologies to help understand disease mechanisms and reveal biomarkers within 1 year, 3) Obtain CADASIL-related grant funding within 1 year, 4) Help train and build the community, and hold a research symposium within 2 years,5) Create model systems built so biomarker conservation can be assessed and high-throughput drug screens performed within 3 years. Exibir menos

Glafabra Therapeutics
Jan 2024 - nowChief Executive OfficerAt Glafabra Therapeutics we are building durable cell therapies for enzyme deficiency disorders that effect 80M patients worldwide. Our lead asset GT-GLA-S03 is in Fabry disease ant its therapeutic durability is now well documented in publications of Canadian clinical trials. Other diseases targets in metabolic disorders are under development using our STEM, TRAM and iTRAM technologies.
Licenses & Certifications
- View certificate

Unconscious Bias
LinkedInJan 2020
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