Aevi Genomic Medicine
- Company typePrivate
- Founded2000
- HeadquartersWayne, United States
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Aevi Genomic Medicine does
Aevi Genomic Medicine is a publicly traded (NASDAQ: GNMX) clinical-stage biopharmaceutical company founded in 2000 and headquartered in Wayne, United States. Per the company's own description, it focuses on translating genetic discoveries into novel therapies, with an operating emphasis on rare and neurodevelopmental disease given its 2015 acquisition of neuroFix Therapeutics and its translational research partnership with The Children's Hospital of Philadelphia, which led a $28M financing round in October 2017.
The company is small (11-50 employees) and has funded operations almost entirely through equity capital rather than product revenue. Across nine disclosed financing rounds since 2001, Aevi has raised approximately $78.5M in aggregate, with investors historically including Alta Berkeley Venture Partners, Alta Partners, and Koor Corporate Venture Capital, and most recently an undisclosed lead in a $4.9M round on 2018-08-21. Leadership consists of Michael F. Cola as President & CEO and John Leaman as CFO.
The business model is preclinical/clinical-development oriented: Aevi monetizes its pipeline through eventual commercialization, licensing, or partnership transactions rather than current product sales. Its go-to-market therefore depends on progressing therapeutic candidates through clinical milestones to attract either a strategic acquirer or commercialization partner. No pricing, distribution, customer segment, or marketing channel information is disclosed in the input data, consistent with a pre-commercial biotech.
Aevi Genomic Medicine firmographics
Firmographics- Name
- Aevi Genomic Medicine
- Website
- https://aevigenomics.com
- Company type
- Private
- Founded year
- 2000
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Ownership category
- akta.pro rank
Aevi Genomic Medicine industry classification
Industry- Product category
- Genomic Medicine Therapeutics
- NAICS
- Research and Development in Biotechnology (except Nanobiotechnology) (541714)
- SIC
- Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
- akta.pro primary industry
- Genetic & Genomic Rare Disease Therapeutics (HLAIAIAA)
- akta.pro secondary industries
- Neurology/CNS Gene Therapies (HLAAACAH), Molecular Diagnostics & Genomics Laboratories (HLAFAMAE)
Keywords
Where Aevi Genomic Medicine is headquartered
LocationHeadquarters
- HQ city
- Wayne
- HQ country
- United States
- HQ region
- North America
Markets served
Aevi Genomic Medicine business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Personnel, Technology or R&D, Operations
Aevi Genomic Medicine product offering
Product offeringCore offering
Aevi Genomic Medicine focuses on translating genetic discoveries into novel therapies, targeting rare and orphan diseases with a particular emphasis on neurological and neurodevelopmental disorders. The company is a clinical-stage biotechnology firm developing pharmaceutical treatments based on genomic insights.
Differentiator
Problem solved
Functional benefit
Products and services
- Genomic-based novel therapies
Companies that use Aevi Genomic Medicine
Customer profileIdeal customer profiles1 record
Aevi Genomic Medicine technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Aevi Genomic Medicine partnerships and signals
Strategic signalRecent moves5 records
Expansion highlights4 records
Aevi Genomic Medicine competitors and assessment
Company assessmentDirect peers
- Audentes Therapeutics: Audentes developed AAV-based gene therapies for rare neuromuscular diseases, a genetic-medicine orientation that mirrors Aevi's stated mission before its acquisition by Astellas.
- Ultragenyx Pharmaceutical: Ultragenyx develops therapeutics for rare and ultra-rare genetic diseases, with multiple programs in metabolic, CNS, and other genetically defined indications — closely paralleling Aevi's focus on genetically driven therapeutics.
- REGENXBIO: REGENXBIO is a clinical-stage gene therapy company developing AAV-based treatments, with CNS and rare-disease programs that overlap directly with the genomic-medicine and neuroFix-related therapeutic areas Aevi has pursued.
- Spark Therapeutics: Spark Therapeutics pioneered AAV-based gene therapies for genetic diseases, including a CNS-directed program, making it a direct historical peer in the genomic-medicine space where Aevi operates.
- Voyager Therapeutics: Voyager focuses on gene therapies for neurological diseases, making it highly comparable to the CNS/neuroFix-related direction Aevi signaled through its 2015 acquisition.
- Neuralstem: Neuralstem is a small clinical-stage biopharmaceutical company developing treatments for CNS and rare neurological conditions, comparable in scale and therapeutic focus to Aevi's neuroFix-related pipeline direction.
- Medgenics: Medgenics is a small-cap public biotech developing therapies for rare and orphan diseases, a comparable profile to Aevi as a sub-scale public genomic-medicine company.
- Dimension Therapeutics: Dimension Therapeutics was a clinical-stage rare-disease gene therapy company targeting genetic diseases including CNS indications, structurally comparable to Aevi's genomic-medicine positioning before its acquisition by Ultragenyx.
Broad incumbents
- BioMarin Pharmaceutical: BioMarin is an established rare-disease therapeutics developer with a focus on genetic and genomic diseases, directly comparable to Aevi's stated mission of translating genetic discoveries into therapies for underserved patient populations.
Others
- Children's Hospital of Philadelphia (CHOP) Research Institute: CHOP is the lead investor from Aevi's 2017 financing round and operates a major pediatric genomic-medicine research program; it is thematically related as a discovery engine and partner in the rare-disease therapeutics pipeline.
Market position
Strengths3 records
Weaknesses4 records
Competitive moat2 records
Key risks5 records
Key highlights5 records
Customer concentration
Aevi Genomic Medicine financial estimates
Financial estimateRevenue estimate
Valuation estimate
Aevi Genomic Medicine leadership team
Management profileNumber of profiles
Profiles2 records
Aevi Genomic Medicine funding detail
Funding detailFunding overview
Funding rounds9 records
Investors4 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Aevi Genomic Medicine M&A and investment
M&A and investmentM&A1 record
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Aevi Genomic Medicine
What does Aevi Genomic Medicine do?
Aevi Genomic Medicine focuses on translating genetic discoveries into novel therapies, targeting rare and orphan diseases with a particular emphasis on neurological and neurodevelopmental disorders. The company is a clinical-stage biotechnology firm developing pharmaceutical treatments based on genomic insights.
When was Aevi Genomic Medicine founded?
Aevi Genomic Medicine was founded in 2000. It employs 11 to 50 people.
Where is Aevi Genomic Medicine based?
Aevi Genomic Medicine is headquartered in Wayne, United States, in the North America region.
Who are Aevi Genomic Medicine's main competitors?
Direct peers on record are Audentes Therapeutics, Ultragenyx Pharmaceutical, REGENXBIO, Spark Therapeutics, Voyager Therapeutics, Neuralstem, Medgenics and Dimension Therapeutics. BioMarin Pharmaceutical is listed as a broad incumbent. Children's Hospital of Philadelphia (CHOP) Research Institute is listed as an others.
Does Aevi Genomic Medicine have an API?
No public API is recorded for Aevi Genomic Medicine.
What industry is Aevi Genomic Medicine in?
Aevi Genomic Medicine's product category is Genomic Medicine Therapeutics. Its primary akta.pro industry code is HLAIAIAA, Genetic & Genomic Rare Disease Therapeutics, with a secondary code of HLAAACAH, Neurology/CNS Gene Therapies. Its NAICS code is 541714 and its SIC code is 2836.