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Collaboration targets lower-dose therapies for genetic muscle disease and in vivo cell therapy.
By: Charlie Sternberg
Margin compression, tariff exposure, and supplier consolidation are piling pressure on contract manufacturers. But single-use technology redrew the competitive landscape and a second wave in cell and gene therapy is doing it again.
By: Dan Stanton
Biotech companies partner to develop low-dose, targeted AAV gene therapies for cardiac disease.
Catalent to support gene therapy manufacturing for SPG50 and other pipeline programs.
Addresses manufacturing challenges related to scalability, cost of goods and process consistency as gene therapy programs move toward commercialization.
Epicrispr’s investigational gene therapy, EPI-321, is a treatment for facioscapulohumeral muscular dystrophy.
By: Patrick Lavery
To create US-APAC manufacturing corridor, enabling local production for global clinical trials.
By: Kristin Brooks
Forge Biologics will provide process development and manufacturing services to support gene therapy for ultrarare disease.
Will apply the AAV Curator Platform to manufacture clinical grade AAV for Drake Rayden Foundation for the treatment of nonketotic hyperglycinemia.
Potency assays are central to proving a therapy activity and safety.
Released By Solvias
Notable pitfalls in the cell and gene therapy space can be addressed with specific aspects of digitalization.
By: Anshul Mangal
Pitcher offers experience scaling cell and gene therapy manufacturing operations and aligning them with client and patient needs.
The program aims to expedite the development of technologies and life-changing therapies for patients in need.
AGC Biologics to provide GMP manufacturing for AAVantgarde’s two novel candidates designed to address progressive and irreversible vision loss.
Expands the company’s nationwide network supporting cell and gene therapy (CGT) innovation.
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