Compositions and methods for ribonuclease-based therapeutics
The present invention relates generally to conjugates of human ribonucleases and water-soluble polymers, compositions comprising the conjugates and methods of using the same. In particular, the present invention provides conjugates of human ribonucleases and one or more water-soluble polymer compositions (e.g., to increase serum half-life and a pharmacokinetic profile, in vivo biological activity, stability, and/or reduce host immune response to the protein in vivo) as well as methods of using the conjugates in the therapy, treatment, and/or prevention of disease (e.g., cancer).
1. A method of treating a human subject having cancer comprising administering to said human subject a composition comprising a human ribonuclease conjugated to a water-soluble polymer, wherein said human ribonuclease is a variant human ribonuclease 1 (RNase 1) comprising a G89C variation of SEQ ID NO: 1, wherein said water soluble polymer is monomethoxy-polyethylene glycol-maleimide, wherein said monomethoxy-polyethylene glycol-maleimide has a molecular weight of between 5 and 60 kDa, and wherein said monomethoxy-polyethylene glycol-maleimide is attached to the cysteine at position 89; wherein said composition is administered under conditions such that tumor growth associated with said cancer is inhibited.
2. The method of claim 1 , wherein said RNase 1 monomethoxy-polyethylene glycol conjugate comprises two methoxy-polyethylene glycol molecules.
3. A method of treating a human subject having cancer comprising administering to said human subject a composition comprising a human ribonuclease conjugated to a water-soluble polymer, wherein said human ribonuclease is a variant human ribonuclease 1 (RNase 1) comprising a G89C variation of SEQ ID NO: 1, wherein said water soluble polymer is monomethoxy-polyethylene glycol-maleimide, wherein said monomethoxy-polyethylene glycol-maleimide has a molecular weight of between about 30 and about 60 kDa, and wherein said monomethoxy-polyethylene glycol-maleimide is attached to the cysteine at position 89; wherein said composition is administered under conditions such that tumor growth associated with said cancer is inhibited.