Granted Patent B2

US 7,125,858 · App. 10/168,327 · Granted Oct 24, 2006

Abstract

Claims (24)

1. A composition comprising purified hyaluronic acid, a second anti-neoplastic agent and a pharmaceutically acceptable carrier, wherein the second anti-neoplastic agent is Mycobacterium phlei DNA (M-DNA), Mycobacterium phlei cell wall complex (MCC), an oligonucleotide, or a combination thereof, wherein the oligonucleotide is SEQ ID NO:1 or SEQ ID NO: 2.

2. A method comprising administering a composition comprising purified hyaluronic acid, a second anti-neoplastic agent and a pharmaceutically acceptable carrier to a mammal having cancer in an amount effective to treat the cancer,

wherein the second anti-neoplastic agent is Mycobacterium phlei DNA (M-DNA), Mycobacterium phlei DNA (M-DNA)- Mycobacterium phlei cell wall complex (MCC), an oligonucleotide, tamoxifen, or a combination thereof, and wherein the oligonucleotide is SEQ ID NO: 1 or SEQ ID NO: 2.

3. A method comprising administering a composition comprising purified hyaluronic acid, a second anti-neoplastic agent and a pharmaceutically acceptable carrier to a mammal having cancer in an amount effective to treat the cancer,

wherein the second anti-neoplastic agent is a Mycobacterium phlei DNA (M-DNA), Mycobacterium phlei DNA (M-DNA)- Mycobacterium phlei cell wall complex (MCC), an oligonucleotide or tamoxifen,

wherein the oligonucleotide is SEQ ID NO: 1 or SEQ ID NO: 2, and,

the cancer is squamous cell carcinoma, fibrosarcoma, sarcoid carcinoma, melanoma, mammary cancer, lung cancer, colorectal cancer, renal cancer, osteosarcoma, cutaneous melanoma, basal cell carcinoma, pancreatic cancer, bladder cancer, brain cancer, ovarian cancer, prostate cancer, leukemia or lymphoma.

4. The composition of claim 1 , wherein the purified hyaluronic acid is hyaluronan, hyaluronate, a salt of hyaluronic acid, a homologue, an analogue, a derivative, a complex, ester, fragment or subunit of hyaluronic acid that is suitable for use in a mammal.

5. The composition of claim 1 , wherein the pharmaceutically acceptable carrier is a liquid carrier, a solid carrier or a combination thereof.

6. The composition of claim 5 , wherein the liquid carrier is water, saline, a physiologically acceptable buffer, an aqueous suspension, an oil emulsion, a water-in-oil emulsion, a water-in-oil-in-water emulsion, a site-specific emulsion, a long residence emulsion, a sticky emulsion, a microemulsion, a nanoemulsion, a mineral oil, neutral oil or mixture thereof.

7. The composition of claim 5 , wherein the solid carrier is a chemical carrier, a biological carrier, a particle, a microparticle, a nanoparticle, a microsphere, a nanosphere, a minipump, a bacterial cell wall extract, a biodegradable or non-biodegradable natural or synthetic polymer that allow for sustained release of the composition, or a mixture thereof.

8. The method of claim 2 , wherein the cancer is squamous cell carcinoma, fibrosarcoma, sarcoid carcinoma, melanoma, mammary cancer, lung cancer, colorectal cancer, renal cancer, osteosarcoma, cutaneous melanoma, basal cell carcinoma, pancreatic cancer, bladder cancer, brain cancer, ovarian cancer, prostate cancer, leukemia or lymphoma.

9. The method of claim 2 , wherein the administering is oral, topical, subcutaneous, transdermal, subdermal, intra-muscular, intra-peritoneal, intra-vesical, intra-articular, intra-arterial, intra-venous, intra-dermal, intra-cranial, intra-lesional, intra-tumoral, intra-ocular, intra-pulmonary, intra-spinal, nasal inhalation, pulmonary inhalation, impression into skin, electroporation, through an osmotic minipump, or through a cannula to the site of interest.

10. A method comprising administering a composition comprising purified hyaluronic acid, a second anti-neoplastic agent and a pharmaceutically acceptable carrier to a mammal having cancer in an amount effective to treat the cancer,

wherein die second anti-neoplastic agent is Mycobacterium phlei DNA (M-DNA), Mycobacterium phlei DNA (M-DNA)- Mycobacterium phlei cell wall complex (MCC), or an oligonucleotide, or a combination thereof, wherein the oligonucleotide is SEQ ID NO: 1 or SEQ ID NO: 2.

11. The method of claim 10 , wherein the cancer is squamous cell carcinoma, fibrosarcoma, sarcoid carcinoma, melanoma, mammary cancer, lung cancer, colorectal cancer, renal cancer, osteosarcoma, cutaneous melanoma, basal cell carcinoma, pancreatic cancer, bladder cancer, brain cancer, ovarian cancer, prostate cancer, leukemia or lymphoma.

12. The method of claim 10 , wherein the administering is oral, topical, subcutaneous, transdermal, subdermal, intra-muscular, intra-peritoneal, intra-vesical, intra-articular, intra-arterial, intra-venous, intra-dermal, intra-cranial, intra-lesional, intra-tumoral, intra-ocular, intra-pulmonary, intra-spinal, nasal inhalation, pulmonary inhalation, impression into skin, electroporation, through an osmotic minipump, or though a cannula to the site of interest.

13. The composition of claim 1 , wherein the purified hyaluronic acid has a molecular mass of between about 1×10 3 and 1×10 7 Daltons.

14. The composition of claim 1 , wherein the purified hyaluronic acid has a molecular mass of between about 5×10 4 and 1×10 6 Daltons.

15. The composition of claim 1 , wherein the purified hyaluronic acid has a molecular mass of between about 1×10 4 and 8×10 5 Daltons.

16. The method of claim 2 , wherein the amount of purified hyaluronic acid administered per dose is about 0.001 to about 25 mg per kg body weight.

17. The method of claim 2 , wherein the amount of purified hyaluronic acid administered per dose is about 0.01 to about 10 mg per kg body weight.

18. The method of claim 10 , wherein the amount of purified hyaluronic acid administered per dose is about 0.001 to about 25 mg per kg body weight.

19. The method of claim 10 , wherein the amount of purified hyaluronic acid administered per dose is about 0.01 to about 10 mg per kg body weight.

Assignments (12)