Events › Healthcare & MedTech
Healthcare & MedTech
5th edition
The 5th In Vivo Cell Engineering & Gene Editing Summit is a 3-day conference in Boston focusing on advancing in vivo delivery platforms, gene editing tools, and translational strategies for genetic medicines, featuring speakers from biopharma and biotech.
Attendees: Scientists, translational leaders, and strategic decision-makers in cell/gene therapy
Exhibitor mix: Categorized by partner type (Expertise, Innovation, Exhibition, Event)
Filter this event to your ICP.
Dozens of solution providers here. You probably care about 20–30. Tell us your ICP, we'll find them.
Request intelligence →Delivery within 24 hours · $1,250
Organizer
Hanson WadePE-backed · London, United Kingdom · Founded 2008
Hanson Wade is a global conference organizer and market intelligence provider focused primarily on the life sciences and biopharma sectors.
Why people attend
Networking with biopharma, biotech, and academic leaders to discuss translational strategies and emerging delivery technologies for in vivo gene editing.
Exhibitor categories
Sample matches
Filtered to a Series-B SaaS ICP. Your filter will be different.
Sample Match A
example.com
"Strong ICP match: Series B, EU expansion, VP Engineering and CTO attending."
Sample Match B
example.io
"Mid-stage SaaS with active GTM motion; product-led growth signals align with ICP."
████████ ██████
████████.io
"████████████████████████████████████████."
Submit your ICP
to unlock all matches
████████ ██████
████████.io
"████████████████████████████████████████."
Submit your ICP
to unlock all matches
Speakers
23 speakers at In Vivo Cell Engineering & Gene Editing Summit
Head of Immunology Search and Evaluation · Abbvie
"Search, Evaluation & Investment Panel: Understanding the Role of In Vivo Therapeutic in Shifting Investor & Pharma Strategies"
Vice President, In Vivo Cell Therapies · Velvet Therapeutics
"Exploring a Differentiated DNA Based Delivery Platform Bridging LNP & Lentiviral Modalities for Safer In Vivo CAR Applications"
Dr. Bagashev is the VP of In Vivo Cell Therapies at Velvet Therapeutics, where he leads strategic development of next-generation CAR based immunotherapies. He brings extensive expertise in immuno-oncology and cell therapies, with publications spanning engineered CAR constructs and immune-modulating platforms. Previously, at Carisma Therapeutics, he advanced preclinical proof-of-concept in vivo CAR-M programs for solid tumors using mRNA/LNP delivery systems. Before Carisma Therapeutics, he contributed to translational ex vivo CAR-T research at Children’s Hospital of Philadelphia and the University of Pennsylvania. His work integrates synthetic biology, vector engineering, and tumor immunology to develop scalable and affordable In Vivo CAR cellular therapies for solid tumors.
Senior Director Business Development Search & Evaluation · AstraZeneca
"Search, Evaluation & Investment Panel: Understanding the Role of In Vivo Therapeutic in Shifting Investor & Pharma Strategies"
Vice President - Urea Cycle Disorders & Therapeutic Area Lead · iECURE
"Examining Clinical Trial Progress & Adaptive Strategies for Safer In Vivo Gene Editing"
George Diaz, M.D., Ph.D., currently serves as VP, Therapeutic Area Lead for Urea Cycle Disorders (UCDs) at iECURE. Dr. Diaz joins the company with more than 25 years of experience in genetics and pediatrics, particularly in metabolic diseases and monogenic disorders. Most recently, he served as chief of the division of Medical Genetics and professor in the Departments of Genetics & Genomic Sciences and Pediatrics at Icahn School of Medicine at Mount Sinai in New York.
Also speaking at International Conference on Neurology and Brain Disorders
Chief Executive Officer · OneChain Immunotherapeutics
"A Novel Differentiated In Vivo Lentiviral Platform"
Stefanos Theoharis brings over 20 years of broad experience in the cell and gene therapy space, business development, program management, manufacturing and basic research brings a deep knowledge CGT sector. Former CBO of Bone Therapeutics, Belgium-based company, developing specialized cell therapies for orthopaedic disorders. Prior to that he was Senior Vice-President at Cell Medica, and CBO at apceth GmbH. He also held positions, among others, as Director Business Development at Roche, focused on partnering activities in emerging science and technologies and M&A Analyst at Lazard, the global investment bank. He holds a PhD in gene therapy and immunology from Imperial College London.
Also speaking at Advanced Therapies Europe 2026, Advanced Therapies Week
CSO · CorriXR Therapeutics
"In Vivo Gene Editing for the Treatment of Squamous Cell Carcinomas, a Direct Platform Approach"
Dr. Kmiec is a pioneering molecular biologist and a leading authority in gene editing and genetic therapies. He is the Founder and Executive Director of ChristianaCare’s Gene Editing Institute, where he has spearheaded groundbreaking research in CRISPR-based technologies, particularly targeting inherited disorders and cancer. Dr. Kmiec is also the Founder and CEO of CorriXR Therapeutics advacing in vivo CRISPR directed gene editing for the treatment of squamous cell carcinoma. He holds academic appointments at the University of Delaware and the Wistar Institute.
Cso · Alaya.bio
Chief Executive Officer & Founder · AllerGene AI Therapeutics
CDO · Asgard Therapeutics
Scientific Co-Founder · Azalea Therapeutics
Chief Scientific Officer · CREATE Medicines
Vice President, Research · GigaMune
Executive Vice President & Chief Scientific Officer · Sana Biotechnology
Chief Scientific Officer · Stylus Medicine
Chief Development Officer · nChroma Bio
"Optimizing Editing & Payload Strategies for Durable In Vivo Programming"
Dr. Jenny Marlowe serves as Chief Development Officer of nChroma Bio, bringing extensive expertise in research and development, gene therapy, and translational sciences. She joined nChroma in December 2024, following her role as Chief Development Officer at Chroma Medicine, where she led development efforts through its merger with Nvelop Therapeutics. Prior to Chroma Medicine, Jenny was Chief Scientific Officer at Solid Biosciences, overseeing R&D efforts for gene therapy programs targeting neuromuscular and genetic cardiomyopathy indications. She also served as Chief Scientific Officer of AavantiBio, where she led scientific strategy until the company’s acquisition by Solid Biosciences.
Director, Nanoparticle Formulation · Beam Therapeutics
+ 7 more speakers at this event.
More Healthcare & MedTech events
Frequently asked questions