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Lonza and InduPro to collaborate on next-gen ADC therapies

Lonza and InduPro have signed a licensing agreement to advance next-generation antibody-drug conjugates (ADC) therapies.
Under the terms of the agreement, Lonza will grant InduPro a non-exclusive, worldwide license to its proprietary GlycoConnect, HydraSpace and linker-payload technologies. These technologies will be applied to the development of ADCs targeting up to two oncology antigens, supporting the advancement of highly targeted cancer therapies.
InduPro will then combine its proprietary bispecific antibody capabilities with Lonza’s ADC platform, including GlycoConnect, HydraSpace, and SYNtecan E. By leveraging these complementary technologies, the companies aim to develop differentiated therapeutic approaches designed to address complex diseases such as cancer, where precision targeting and efficacy remain critically important.
“We are pleased to be starting this collaboration with InduPro, which underscores the strength and versatility of our ADC platform,” said Jan Vertommen, Vice President of Commercial Development, Advanced Synthesis at Lonza.
“By combining our expertise in bioconjugation technologies and manufacturing with InduPro’s innovative proximity guided antibody platform, we reinforce our commitment to enabling our licensing partners and supporting the advancement of next-generation ADC programmes.”
“This agreement represents an important step in advancing our pipeline of proximity-driven bispecific ADCs,” added Prakash Raman, CEO of InduPro.
“By combining InduPro’s ability to identify novel, disease-specific co-target pairs with Lonza’s industry-leading ADC technologies, we aim to develop differentiated, first-in-class therapeutics that improve selectivity, expand therapeutic windows, and ultimately deliver better outcomes for patients with hard-to-treat tumours.”
The post Lonza and InduPro to collaborate on next-gen ADC therapies appeared first on Drug Discovery World (DDW).
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STAT+: Biosecure didn’t stop China’s rise in biotech. Some lawmakers want to do more
WASHINGTON — Last year, Congress passed a bill restricting how U.S. pharmaceutical and biotechnology companies can do business with Chinese firms. Many political leaders don’t seem to be satisfied.
Already, they’re laying the groundwork for additional legislative and regulatory measures to counter the rise of Chinese biopharma companies. And federal health officials are working to make it easier for companies to operate in the U.S.
“The itch has not been entirely scratched,” said Bobby McMillin, partner at Arnold Porter.
WASHINGTON — Last year, Congress passed a bill restricting how U.S. pharmaceutical and biotechnology companies can do business with Chinese firms. Many political leaders don’t seem to be satisfied.
Already, they’re laying the groundwork for additional legislative and regulatory measures to counter the rise of Chinese biopharma companies. And federal health officials are working to make it easier for companies to operate in the U.S.
“The itch has not been entirely scratched,” said Bobby McMillin, partner at Arnold Porter.
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Labs see rising demand for nitrosamine, topical performance and microbiome testing
Recent BioSpace industry conference conversations point to sponsors pushing earlier on safety, quality and performance data, leading to demand for nitrosamine analysis, IVRT/IVPT and microbiome database capabilities.
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10 companies hiring in San Francisco, South San Francisco (plus a few in Brisbane, San Rafael)
10 companies hiring in San Francisco, South San Francisco (plus a few in Brisbane, San Rafael)
Looking for a new role in and around San Francisco? Check out these companies hiring across all disciplines. Read More
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