About Gene Thrive
Thriving Tomorrow: Precision Editing and Scalable Solutions for Common Diseases
Gene Thrive 2026 was founded on the principle that the "proof of concept" era for gene therapy is now behind us. As we navigate the realities of 2026, the industry is no longer just asking if we can edit the human genome, but how we can do so with surgical precision for millions of patients. Our summit serves as the critical bridge between groundbreaking academic research and large-scale industrial execution. We are dedicated to catalyzing the shift from treating rare, ultra-orphan conditions to addressing the world’s most prevalent chronic diseases, including cardiovascular failure, neurodegeneration, and metabolic disorders.
Our mission is to dismantle the bottlenecks that prevent life-altering therapies from reaching the bedside. While discovery remains vital, the current landscape demands a relentless focus on the "Last Mile"—the complex intersection of AI-optimized manufacturing, scalable delivery platforms, and sustainable reimbursement models. Gene Thrive 2026 brings together the architects of the new bio-economy: from the scientists engineering the next generation of non-viral vectors to the industrial leaders building the modular factories of the future. We provide the forum where Chemistry, Manufacturing, and Controls (CMC) excellence meets regulatory harmony to ensure global patient access.
Speaker Application FormStep into the industrial era of genetic medicine at Gene Thrive 2026. Beyond the laboratory, we are gathering the architects of scale—visionaries bridging the gap between breakthrough science and global patient access. Join 500+ industry leaders in San Diego to master the complexities of precision editing, AI-driven manufacturing, and the commercial transition to prevalent diseases. The future isn't just taking shape; it’s being built here.
Gene Thrive 2025 Speakers
Fyodor Urnov
Scientific Director, Innovative Genomics Institute
TBA
Basel Assaf
Distinguished Scientist, Preclinical Safety, Sanofi
Considerations for successful design and execution of IND enabling studies for in vivo gene therapy products
Sandra Ammann
Institute for Immunodeficiency Center for Chronic Immunodeficiency Medical Center – University of Freiburg
Under the Molecular Lens: Novel Assays to Identify Unpredictable Off-Target and Structural Effects in Genome Editing
Amy Raymond
Executive Director, Therapeutic Strategy Lead, Worldwide Clinical Trials
Optimizing Gene Editing Trials for Rare Disease Patient Populations
Why Attend Gene Thrive 2025
GeneThrive 2025 offers a unique opportunity for professionals across various sectors to come together and participate in a transformative event focused on gene therapy. Here are several compelling reasons why individuals should attend:
Stay Updated on the Latest Advancements
Gene Thrive provides access to cutting-edge research and breakthrough technologies.
Networking and Collaboration
A platform for networking and collaboration among industry leaders, researchers, and other stakeholders.
Professional Development
Gain invaluable insights and skills through keynote presentations, discussions, and interactive sessions.
Access to Expertise
Engage with experts, thought leaders, and key opinion leaders in the gene therapy field.
Influence and Impact
Influence the direction of gene therapy advancements and policy shaping future developments.
Inspiration and Motivation
Be inspired by innovative research and patient success stories, fueling your own passion in the field.
Agenda at a Glance
CRISPR and Beyond: Innovations in Gene Editing
This session will delve into the latest advancements in gene editing technologies, including CRISPR/Cas9, base editing, and prime editing. Experts will discuss their applications in therapeutic development, challenges, and future prospects.
Precision Gene Editing with Base Editors
Explore base editing, the game-changer enabling pinpoint single-nucleotide tweaks without risky double-strand breaks. Experts will break down its mechanics, spotlight its role in drug development, and weigh its limits—plus tease recent leaps and where it’s headed.
Prime Editing: Rewriting the Genetic Code
Get the inside track on prime editing, a breakthrough tech rewriting DNA with surgical precision—insertions, deletions, or swaps, no compromises. Leaders will reveal how it works, its therapeutic potential, and the challenges ahead, showcasing why it’s a big deal for the industry.
Next-Generation Gene Editing Platforms
Discover the cutting-edge tools pushing beyond CRISPR—think homing endonucleases, transposon systems, and synthetic nucleases. This subsession spotlights how these platforms are reshaping research and therapies, with insights into their practical impact and future promise.
Viral Vectors: Engineering the Perfect Carrier
Dive into viral vectors, the workhorses of gene therapy delivery. Experts will unpack cutting-edge engineering tricks—boosting safety, dodging immune blowback, and maxing out efficiency—while confronting the real-world hurdles holding them back.
Non-Viral Delivery Systems
Explore the rising stars of gene delivery—liposomes, nanoparticles, polymers, and cell-penetrating peptides. Leaders will weigh their edge over viral options, dissect limitations, and showcase breakthroughs that amp up targeting and payload punch.
Genome Editing Delivery: CRISPR Carriers
Get the lowdown on delivering CRISPR-Cas systems for precision edits. This subsession covers viral and non-viral strategies, spotlighting how to optimize for target cells, sidestep pitfalls, and unlock CRISPR’s full therapeutic potential.
Targeted Delivery: Precision Medicine Approaches:
Crack the code on hitting the bullseye with gene therapies. Experts will dive into ligand-guided targeting, tissue-specific promoters, and other precision tactics—showing how to sharpen specificity, cut off-target noise, and boost clinical impact.
Genetic Disorders: Therapeutic Breakthroughs:
Dive into gene therapy’s impact on genetic disorders—think cystic fibrosis, muscular dystrophy, and sickle cell disease. Experts will reveal recent wins, unpack active trials, and tackle the leap from preclinical promise to bedside reality.
Cancer Immunotherapy: Targeting Tumor Cells: Advances in Base Editing:
Explore gene therapy’s arsenal against cancer—CAR-T cells, adoptive transfers, and oncolytic viruses. Leaders will break down cutting-edge advances, clinical results, and the next wave of strategies to wipe out tumors with precision.
Neurodegenerative Diseases: Promising Interventions:
Unlock gene therapy’s potential for neurodegenerative foes like Parkinson’s, Alzheimer’s, and ALS. This subsession digs into novel delivery tactics, editing tools, and emerging targets aimed at halting these diseases at their roots.
Infectious Diseases: Gene-Based Strategies:
Fight back against infections—viral, bacterial, and beyond—with gene therapy. Experts will showcase gene-driven vaccines, antivirals, and immune boosts, plus explore how editing can outsmart pathogens and fortify host defenses.
Informed Consent and Autonomy
Unpack the messy reality of consent in gene therapy trials. Leaders will tackle how to secure genuine buy-in, clarify risks versus rewards, and shield vulnerable groups—ensuring trials don’t just push science but respect patients.
Equity and Access
Face the hard truth about who gets gene therapies—and who doesn’t. Experts will dissect barriers like sky-high costs, spotty insurance, and uneven healthcare systems, pitching bold fixes to level the playing field for all patients.
Privacy and Genetic Data
Dive into the minefield of genetic data—privacy risks, security gaps, and legal gray zones. This subsession spotlights how to safeguard sensitive info, meet regs, and steward data responsibly in research and practice.
Social and Cultural Implications
Explore how society views gene therapy—hype, fear, or something else? Experts will decode cultural drivers of acceptance or pushback, sharing ways to build trust and inclusivity across research, education, and care.
Next-Generation Therapeutic Modalities:
Uncover the tools rewriting gene therapy’s playbook—RNA therapies, in vivo editing, and synthetic biology. Experts will spotlight their game-changing potential, real-world applications, and the hurdles to bringing them to market.
Personalized Medicine and Gene Editing:
See how gene editing meets precision medicine head-on. Leaders will dive into genome sequencing breakthroughs, biomarker wins, and patient-tailored edits—showing how to craft therapies as unique as the people they treat.
Gene Therapy for Rare Diseases:
Tackle rare diseases with gene therapy’s firepower. This subsession digs into fast-tracking solutions for unmet needs—think streamlined regs, patient advocacy, and team-ups that turn orphan drugs into reality.
Regulatory and Policy Landscape:
Navigate the shifting rules and red tape of gene therapy. Experts will break down regulatory roadblocks, policy shifts, and what’s coming next to keep innovation safe, ethical, and on track for the clinic.
Interested in Sponsoring Gene Thrive 2025?
If your company is interested in sponsoring Gene Thrive 2025, we would be delighted to discuss the opportunities with you. Please send us a quick email, and we will promptly provide you with more information and our sponsorship brochure.
Sponsors
Gene Thrive 2025: Advancing Innovation, Transforming Lives: The Future of Gene Therapy Starts Here
Venue
AC Hotel Barcelona Forum
Paseo Taulat 278, Barcelona, 08019
Spain


Contact
Address
259, Narendra Colony, Hyderabad, Telangana 502032
Call Us
+91 9059841607
Email Us
jyothi@pharmasynergevents.com
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