• High Performance: Stable adeno-associated virus (AAV) cell line development service results in titers up to 6E15 vg/L before purification, in under 20 weeks.
  • Improved Quality: Fully stable clonal cell lines integrate all essential viral genes and transgenes, reducing batch variability and delivering more consistent product quality.
  • Reduced Cost of Goods: Transfection-free AAV manufacturing eliminates GMP plasmid costs while reducing supply chain risk, enabling greater scalability, and lowering batch-failure risk.

Boston, MA, October 6, 2025–Asimov, the synthetic biology company advancing the design and manufacture of therapeutics, today announced the launch of its AAV Edge Stable Producer System. With this launch, Asimov aims to address the shortcomings of traditional transient transfection-based production and bring AAV manufacturing standards closer to those established for antibody-based biologics.

A major challenge in AAV gene therapy has been developing scalable, cost-efficient processes to reliably produce high-quality vectors. Most programs still depend on transient production, which requires multiple GMP plasmids to be transfected every batch. This approach drives up costs, introduces supply chain risk, limits bioreactor scalability, and can potentially result in inconsistent product quality.

Asimov’s AAV Edge Stable Producer System brings AAV manufacturing in line with the gold-standard practices long established in protein biologics. By stably integrating all essential viral genes into the genome of HEK293 cells, Asimov generates high-titer, clonal producer cell lines. Stable clones eliminate the need for costly GMP plasmids, enable straightforward scale-up in bioreactors, and minimize batch-to-batch variability. The result is lower manufacturing cost, more consistent product quality, and the potential for safer, more effective AAV gene therapies.

Asimov’s new offering delivers research cell banks (RCBs) within 20 weeks that contain the desired capsid and transgene. Therapeutic developers receive clonal, suspension-adapted, fully stable AAV HEK293 producer cell lines that enable reliable manufacture of gene therapies at scale, with titers up to 6E15 vg/L before purification.

“It’s no secret that the gene therapy field has gone through several painful years recently, but the fact is that gene therapy remains our best shot at treating many of the world’s most intractable diseases. We firmly believe in the potential of this modality, and stand alongside the patients and scientific pioneers who continue to push the field forward,” said Alec Nielsen, co-founder and CEO of Asimov. “Together, we're pulling every lever available to improve scalability, safety, efficacy, quality, and cost. Stable producer cell lines are one of the technologies needed to unlock the next generation of gene therapies. I’m incredibly proud of our team for achieving this technical milestone in synthetic biology, and excited by the validation we’re receiving from pharma partners on their gene therapy programs.”

Today’s launch further expands Asimov’s offerings in cell and gene therapy, which now include stable producer systems for both lentiviral and AAV manufacturing. Additionally, the AAV Edge Stable Producer System complements Asimov’s existing AAV payload design capabilities, which include tissue specific promoters and expression optimization tools. To learn more about the AAV Edge Stable Producer System, please visit https://www.asimov.com/aav-edge-system?tab=aav-stable-production.

About Asimov

Asimov’s mission is to advance humanity’s ability to design living systems, enabling biotechnologies with outsized societal benefit. The company is developing a synthetic biology platform – from cells to software – to design and manufacture next-generation therapeutics, including biologics, cell/gene therapies, and RNA through a combination of products, services, and collaborations.  

Founded by bioengineers from MIT and Boston University and headquartered in Boston, the company has raised over $200 million from top institutional investors including Andreessen Horowitz, CPP Investments, Horizons Ventures, and Fidelity Management & Research Company. For more information, visit www.asimov.com.  

Highlights

  • Virtual Private Network (VPN): Users connect to the cluster, provide some credentials and are then able to access internal tools.
  • Single Sign-On: A tool like Kerberos allows you to use the same account across various components.
  • Home-grown user accounts: You implement an authentication system and users have a separate username/password for your computing infrastructure.

Asimov, the synthetic biology company building a full-stack platform to program living cells, announced today it has been awarded a contract as part of the Defense Advanced Research Projects Agency (DARPA) Automating Scientific Knowledge Extraction (ASKE) opportunity.

Through ASKE, Asimov will work to develop a physics-based artificial intelligence (AI) design engine for biology. The goal of the initiative is to improve the reliability of programming complex cellular behaviors.

“To achieve truly predictive engineering of biology, we require dramatic advances in computer-aided design. Machine learning will be critical to bridge genome-scale experimental data with computational models that accurately capture the underlying biophysics. As genetically engineered systems grow in complexity, they become difficult for humans to design and understand. For simple genetic systems with only a couple of genes, synthetic biologists typically use high-throughput screening and basic optimization algorithms. But to engineer more complex applications in health, materials, and manufacturing, we need radically new algorithms to intelligently design the DNA and simulate cell behavior.”

Alec Nielsen, Phd, Asimov CEO
Over the past 50 years, DARPA has been a world leader in spurring innovation across the field of AI, including statistical-learning and rule-based approaches. We are proud to work with DARPA to advance the state-of-the-art in AI-assisted genetic engineering.

Asimov’s founders previously built a hybrid genetic engineering and computer-aided design platform called Cello to program logic circuit behaviors in cells. The ASKE opportunity will seek to support an ambitious expansion in the types of biological behaviors that can be engineered.

Asimov’s approach will leverage “multi-omics” cellular measurements, structured biological metadata, and novel AI architectures that combine deep learning, reinforcement learning, and mechanistic modeling. Over the past year, the company has ramped up hiring in experimental synthetic biology, machine learning, and data science to accelerate development of their genetic design platform.

Highlights

Headering 3

DARPA recently announced a multi-year investment of $2B into innovative artificial intelligence research called the AI Next campaign. A part of this wide-ranging AI strategy is DARPA’s Artificial Intelligence Exploration program, which was developed to help expeditiously move pioneering AI research from idea to exploration in fewer than 90 days. DARPA’s ASKE opportunity is part of this program and is focused on developing AI technologies that can reason over rich models of complex systems.

“Over the past 50 years, DARPA has been a world leader in spurring innovation across the field of AI, including statistical-learning and rule-based approaches. We are proud to work with DARPA to advance the state-of-the-art in AI-assisted genetic engineering.”

Alec Nielsen, PhD, Asimov CEO
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