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`This version of the claims will replace all previous versions.
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`1. (Original) A modified PH20 polypeptide, comprising one or more amino acid modifications
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`in an unmodified PH20 polypeptide, wherein:
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`the unmodified PH20 polypeptide consists of the amino acid sequence selected from among
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`SEQ ID NOs: 3, 7 and 32-66;
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`amino acid modifications are selected from among amino acid replacements(s), deletion(s),
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`and/or insertion(s);
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`the modified PH20 polypeptide comprises an amino acid replacementat a position
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`corresponding to residue 324, with reference to amino acid positions set forth in SEQ ID NO:3;
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`the replacementat the position corresponding to residue 324 is selected from amongA,D,
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`H, M, N, Rand S;
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`corresponding aminoacid positions are identified by alignment of the PH20 polypeptide
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`with the polypeptide having the amino acid sequence of SEQ ID NO:3; and
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`the modified PH20 polypeptide has at least 91 % sequence identity to a polypeptide having
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`the amino acid sequenceselected from among SEQ ID NOs: 3, 7 and 32-66.
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`2. (Original) The modified PH20 polypeptide of claim 1, wherein the modified PH20
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`polypeptide has at least 95% sequence identity to the amino acid sequence selected from among
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`SEQ ID NOs: 3, 7, and 32-66.
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`3. (Original) The modified PH20 polypeptide of claim 1 that has increased
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`resistance to or stability in denaturing conditions compared to an unmodified PH20 polypeptide that
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`does not contain the amino acid modification(s).
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`4. (Original) The modified PH20 polypeptide of claim 1 that exhibits increased hyaluronidase
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`activity compared to the unmodified PH20 polypeptide not containing the amino acid replacement
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`at position 324.
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`5. (Original) The modified PH20 polypeptide of claim 1 that is a soluble PH20 polypeptide.
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`6. (Original) The modified PH20 polypeptide of claim 1, wherein the replacementat the
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`position corresponding to residue 324is D.
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`7. (Original) The modified PH20 polypeptide of claim 1, wherein the replacementat the
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`position corresponding to residue 324 is Nor R.
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`8. (Original) The modified PH20 polypeptide of claim 1, wherein the unmodified PH20
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`polypeptide comprises the amino acid sequence selected from among SEQ ID NOs: 3 and 32-66.
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`9. (Original) The modified PH20 polypeptide of claim 1, wherein the unmodified PH20
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`polypeptide consists of the amino acid sequence selected from among SEQ ID NOs: 3 and 32-66.
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`10. (Original) The modified PH20 polypeptide of claim 6, wherein the unmodified PH20
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`polypeptide consists of the amino acid sequence selected from among SEQ ID NOs: 3 and 32-66.
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`DB1i/ 144937442.1
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`2
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`11. (Original) The modified PH20 polypeptide of claim 1, wherein the unmodified PH20
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`polypeptide consists of the amino acid sequence of SEQ ID NO:35.
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`12. (Original) The modified PH20 polypeptide of claim 1, wherein the unmodified PH20
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`polypeptide consists of the amino acid sequence of SEQ ID NO:32.
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`13. (Original) The modified PH20 polypeptide of claim 6, wherein the unmodified PH20
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`polypeptide consists of the amino acid sequence of SEQ ID NO:35.
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`14. (Original) The modified PH20 polypeptide of claim 6, wherein the unmodified PH20
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`polypeptide consists of the amino acid sequence of SEQ ID NO:32.
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`15. (Original) The modified PH20 polypeptide of claim 1, comprising a sequence of amino
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`acids that exhibits at least 91 % sequence identity to the sequence of amino acids set forth in any of
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`SEQ ID NOs: 3, 32-66, 623, and 624 and that contains an amino acid replacementD at the residue
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`correspondingto residue 324 with reference to SEQ ID NO:3.
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`16. (Original) The modified PH20 polypeptide of claim 1 that is C-terminally truncated,
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`wherebythe polypeptide is soluble.
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`17. (Original) The modified PH20 polypeptide of claim 1 that comprises one or more
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`modifications of the polypeptide selected from amongglycosylation, sialylation, aloumination,
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`famesylation, carboxylation, hydroxylation, and phosphorylation.
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`18.
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`19.
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`(Original) The modified PH20 polypeptide of claim 1 that is glycosylated.
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`(Original) The modified PH20 polypeptide of claim 18, wherein the polypeptideis a
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`glycoprotein that comprises an N-acetylglucosamine moietylinked to each of at least three
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`asparagine (N) residues.
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`20. (Original) The modified PH20 polypeptide of claim 1 that is conjugated to a polymer.
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`21. (Original) The modified PH20 polypeptide of claim 20, wherein the polymer is dextran or
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`polyethylene glycol (PEG).
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`22. (Original) The modified PH20 polypeptide of claim 1, further comprising a heterologous
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`signal sequence, wherein the unmodified PH20 polypeptide consists of the amino acid sequence
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`selected from among SEQ ID NOs: 3 and 32-66.
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`23. (Original) A chimeric polypeptide, comprising the modified PH20 polypeptide of claim 1.
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`24. (Original) A pharmaceutical composition, comprising the modified PH20 polypeptide of
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`claim 1.
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`25. (Original) The modified PH20 polypeptide of claim 6, wherein:
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`the unmodified PH20 polypeptide consists of the amino acid sequence of SEQ ID NO:32; and
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`the amino acid sequence of the modified PH20 polypeptide has at least 95% sequence
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`identity to the amino acid sequence of SEQ ID NO:32.
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`26. (Original) The modified PH20 polypeptide of claim 6, wherein:
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`the unmodified PH20 polypeptide consists of the amino acid sequence of SEQ ID NO:35; and
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`DB1i/ 144937442.1
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`3
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`the amino acid sequence of the modified PH20 polypeptide has at least 95% sequence
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`identity to the amino acid sequence of SEQ ID NO:35.
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`27. (Original) The pharmaceutical composition of claim 24, further comprising a
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`therapeutically active agent formulated in the same composition or in a separate composition.
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`28. (Original) The pharmaceutical composition of claim 27, wherein the therapeutically
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`active agent is a polypeptide, a protein, a nucleic acid, a drug, a small molecule, or an organic
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`molecule.
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`29. (Original) The pharmaceutical composition of claim 27, wherein the therapeutically
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`active agentis selected from among a chemotherapeutic agent, an analgesic agent, an anti-
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`inflammatory agent, an antimicrobial agent, an amoebicidal agent, a trichomonacidal agent, an anti-
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`Parkinson agent, an anti-malarial agent, an anticonvulsant agent, an anti-depressant agent, an
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`antiarthritics agent, an anti-fungal agent, an antihypertensive agent, an antipyretic agent, an anti-
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`parasite agent, an antihistamine agent, an alpha-adrenergic agonist agent, an alpha blocker agent,
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`an anesthetic agent, a bronchial dilator agent, a biocide agent, a bactericide agent, a bacteriostat
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`agent, a beta adrenergic blocker agent, a calcium channel blocker agent, a cardiovascular drug
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`agent, a contraceptive agent, a decongestant agent, a diuretic agent, a depressant agent, a
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`diagnostic agent, an electrolyte agent, a hypnotic agent, a hormone agent, a hyperglycemic agent, a
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`muscle relaxant agent, a muscle contractant agent, an ophthalmic agent, a parasympathomimetic
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`agent, a psychic energizer agent, a sedative agent, a sympathomimetic agent, a tranquilizer agent, a
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`urinary agent, a vaginal agent, a viricide agent, a vitamin agent, a non-steroidal anti-inflarmmatory
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`agent, an angiotensin converting enzyme inhibitor agent, and a sleep inducer.
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`30. (Original) The pharmaceutical composition of claim 27, wherein the therapeutically
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`active agent is an antibody.
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`31. (Withdrawn) A methodfor treating a hyaluronan-associated disease or condition,
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`comprising administering to a subject a modified PH20 polypeptide ofclaim 1.
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`32. (Withdrawn) The method of claim 31, wherein the hyaluronan-associated disease or
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`condition is an inflammatory disease or a tumor or cancer.
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`33. (Withdrawn) The method of claim 32, wherein the hyaluronan-associated disease or
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`condition is a solid tumor.
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`34. (Withdrawn) The modified PH20 polypeptide of claim 1 that is modified by conjugation
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`to a moiety selected from among a multimerization domain, a toxin, a detectable label, and a drug.
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`35. (Original) The modified PH20 polypeptide of claim 34, wherein the modified
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`PH20 polypeptide is conjugated to a multimerization domain that is an Fe domain.
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`DB1i/ 144937442.1
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`4
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