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Completion of a “First in Human” Clinical Phase I Study Using CAP® Cells

Published: Tuesday, November 05, 2013
Last Updated: Tuesday, November 05, 2013
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Consortium reported safe completion of clinical study with recombinant human Alkaline Phosphatase (hRESCAP®).

CEVEC Pharmaceuticals (“CEVEC”) has announced that a Dutch consortium led by TNO reported the safe completion of a clinical Phase I study with recombinant human Alkaline Phosphatase (hRESCAP®) derived from CEVEC’s CAP® cells.

The consortium consisting of TNO and Alloksys Life Sciences B.V., among others, performed a dose escalating investigative Phase I study to determine the safety and pharmacokinetics of parenterally delivered hRESCAP® in healthy volunteers.

Paving the path to ultimately treat chronic inflammatory diseases like Rheumatoid Arthritis in AMRIF B.V., a recently founded sister company to Alloksys Life Sciences, the study represents a major milestone for CEVEC since it establishes the CAP® cell line as a regulatory-proven expression host for the broader production of therapeutic proteins, antibodies and vaccines.

CAP® cells are immortalized suspension cells for stable protein production developed by CEVEC. This non-tumor origin cell line exhibits high protein expression, has been adapted to serum-free suspension culture and shows post-translational modifications that are human-like, including authentic human glycosylation patterns.

The Technology allows for superior yields of complex (glyco) proteins in a shorter time frame than traditional methods.

“We’re proud that our long-standing collaboration with Alloksys Life Sciences B.V. to produce recombinant human alkaline phosphatase at high yields and consistent quality in CAP® has succeeded to enter the clinic. The safe and very promising outcome of this study underlines the potential of our human CAP® cells to become a standard expression host for therapeutic and clinically relevant proteins. TNO obtained regulatory approval to conduct a single ascending dose study with hRESCAP® produced with CEVECs expression system. This will certainly facilitate the regulatory acceptance and pave the way for clinical development of all other CAP® -derived therapeutics that are currently at preclinical stage or entering clinical development” stated Wolfgang Kintzel, CEO at CEVEC.


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