| BASEL and GENEVA, February 20, 2004 |
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Lonza and NovImmune announce manufacturing agreement for clinical grade monoclonal antibodies
Basel and Geneva, February 20, 2004 -Lonza, Basel, and the Geneva-based drug
development company NovImmune today announced an agreement for the
production and supply of clinical grade monoclonal antibody drugs, all the way to
market supply. NovImmune develops fully human therapeutic monoclonal
antibodies, based on its direct access to both the transgenic mouse technology (humice) and the antibody display technology. This agreement provides Lonza with
access to the whole pipeline of NovImmune, a potential for the manufacturing of
NovImmune's own products as well as of those developed with or licensed to
partners. Lonza will manufacture the products all the way to market. NovImmune
gains access to Lonza's development and manufacturing capacity.
"We very much look forward to meeting the manufacturing needs of NovImmune
and of its partners. The agreement will initially lead to the production of two
antibodies and provision of GMP material for clinical trials. Lonza is one of the
worlds' leaders in the manufacture of antibodies and is very pleased to have the
opportunity to apply its experience to the products which are being developed by
NovImmune", said Markus Gemuend, CEO of Lonza Group.
"Our manufacturing agreement with Lonza deals with one of the recognized
bottlenecks in the development of therapeutic monoclonal antibodies" said Jack
Barbut, ScD, CEO of NovImmune. "In addition to covering our own immediate
manufacturing needs towards phase I and II clinical trials, this agreement offers our
future licensing partners an access to manufacturing, for each of our products, all
the way to market supply. This adds considerable value to NovImmune's
therapeutic antibody program. NovImmune's focus on immune-related diseases
and inflammation, is supported by strong immunobiology in house and
consequently on unusually stringent biological validation for each of its monoclonal
products. In our view, this is an important asset to minimize the risk of subsequent
failure in clinical trials." Click here to download the press release (.PDF format)
For further information please contact:
Roland Waibel
Walter Eschenmoser |