Site specific in vivo activation of therapeutic drugs
AssigneeAkzo N.V.
InventorsReinhard Bredehorst, Chong-Ho Kim, Richard McCabe, Nicholas Pomato, Carl-Wilhelm Vogel
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AssigneeAkzo N.V.
InventorsReinhard Bredehorst, Chong-Ho Kim, Richard McCabe, Nicholas Pomato, Carl-Wilhelm Vogel
Estimating the term…
A method for site-specific in-vivo activation of a prodrug in an animal using an activator-targeting moiety conjugate to localize an activator at a predetermined site of use and a prodrug compound that is converted to an active drug in the presence of the activator. In the preferred embodiment, the targeting moiety, the activator, and the prodrug demonstrate little or no immunogenicity in the animal being treated. The targeting moiety is relatively specific for binding to the target tissue than to non-target tissue. The activator is not found or present in only small amounts in circulation or in non-target tissue, does not have a substrate for its activity in circulation or in non-target tissue, can be linked to the targeting moiety, and is capable of converting the prodrug to an active drug. The prodrug is selected for its ability to exert a cytotoxic activity on the target tissue after conversion by the activator.
In an improved method for in vivo activation of a prodrug at the location of target tissue in a patient comprising:
An activator-targeting moiety conjugate comprising lysozyme as the activator, wherein the targeting moiety is an antibody selected from the group consisting of a human monoclonal antibody, a monoclonal antibody fragment and a chimeric monoclonal antibody, and whereby said activator-targeting moiety is non-immunogenic in humans.
A prodrug comprising an anthracycline carrying a cleavable molecule that prevents cellular uptake.
Dependencies are inferred from the claim text.