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18B Fraunhoferstrasse, Planegg, 82152, DE
Coriolis Pharma is a global contract research and development organization (CRDO) and the premier partner for the development of liquid and lyophilized drug products, analytical services, and manufacturing services across a vast array of therapeutic modalities, including biologics, gene and cell therapies and vaccines. Our scientists design and execute platform and custom services to accelerate and de-risk your program right from the start and throughout the entire product lifecycle.
Andelyn will use its Curator cell and gene therapy platform to transition Genprex’s candidate in support of clinical trials.
By: Patrick Lavery
The companies will collaborate to advance the treatment through development and FDA approval.
Customers can engage Cytovance for analytical method development, transfer, qualification, validation, product characterization, release testing, stability studies, and storage.
CDMO to manufacture AAV9-GM2 candidate for Tay-Sachs and Sandhoff diseases.
By: Charlie Sternberg
ST-920 is a one-time administered AAV gene therapy undergoing BLA review for Fabry disease.
Nearly half of biopharma companies report difficulty finding mammalian production capacity, while cell and gene therapy face even tighter constraints.
By: Katrina Cordovado
Sponsored By ProBio CDMO
Collaboration combines Circio’s circVec platform with Avenue’s protein engineering technology to improve secretion of therapeutic proteins.
Catalent will support commercial packaging and distribution as Nanoscope advances its rolling BLA submission.
Alliances and expertise behind advancing CGTs in today’s market.
By: Kristin Brooks
Collaboration targets lower-dose therapies for genetic muscle disease and in vivo cell therapy.
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.
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