IP Library Granted Patent US 6,855,338
Granted Patent B2
US 6,855,338 · App. 10/087,041 · Granted Feb 15, 2005

Anti-tumor therapies comprising a combination of a cartilage extract and an anti-neoplastic agent providing high efficacy and low toxic side effects

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Quick Facts
Patent No.
US 6,855,338
App. No.
10/087,041
Granted
Feb 15, 2005
Kind
B2
Abstract

This invention described a novel use for cartilage extract, namely a shark cartilage extract, in a combined anti-tumor therapy. The cartilage extract is used in combination with anti-neoplastics. The combined therapy provides for a higher anti-tumor efficacy with no concomitant increase, even better with a decrease, of toxic side effects.

Claims (31)

1. An anti-tumor composition comprising

an anti-tumor amount of anti-neoplastic agent;

a side effect-reducing amount of a shark cartilage extract; and

a pharmaceutically acceptable carrier.

2. The anti-tumor composition of claim 1 , wherein the anti-neoplastic agent is selected from the group consisting of busulfan, thiotepa, chlorambucil, cyclophosphamide, estramustine sodium phosphate, ifosfamide, mechlorethamine hydrochloride, melphalan, carmustine, lomustine, streptozocin, carboplatin, cisplatin, methotrexate sodium, cladribine, mercaptopurine, thioguanine, cytarabine, fluorouracil, hydroxyurea, daunorubicin, doxorubicin hydrochloride, epirubicin hydrochloride, idarubicin hydrochloride, dactinomycin, bleomycin sulfate, mitomycin, mitotane, mitoxantrone hydrochloride, etoposide, teniposide, docetaxel, paclitaxel, vinblastine sulfate, vincristine sulfate, vindesine sulfate, vinorelbine tartrate, altretamine, amsacrine, 1-asparaginase, dacarbazine, fludarabine phosphate, porfimer sodium, procarbazine hydrochloride, tretinoin (all-trans retinoic acid), marimastat, suramin, TNP 470, thalidomide and radiotherapeutics.

3. The anti-tumor composition of claim 1 , wherein the anti-neoplastic agent is cisplatin.

4. The anti-tumor composition of claim 1 , wherein the shark cartilage extract comprises water-soluble molecules and a major portion of the water-soluble molecules have a molecular weight of less than about 500 kDa.

5. The anti-tumor composition of claim 4 , wherein the shark cartilage extract has been prepared by fractionating a crude shark cartilage extract comprising water-soluble molecules obtained from shark cartilage material such that a major portion of the molecules having a molecular weight of greater than about 500 kDa is separated from a major portion of the molecules having a molecular weight of less than about 500 kDa.

6. The anti-tumor composition of claim 1 , further comprising hypoxanthine.

7. An anti-tumor composition comprising

a sub-optimal dosage amount of an anti-neoplastic agent;

a side effect-reducing amount of a shark cartilage extract; and

a pharmaceutically acceptable carrier that is an aqueous solution,

wherein administration of the anti-tumor composition causes less side effects than administration of a similar composition that does not contain shark cartilage extract.

8. An anti-tumor composition comprising

an optimal dosage amount of an anti-neoplastic agent;

a side effect-reducing amount of a shark cartilage extract; and

a pharmaceutically acceptable carrier that is an aqueous solution,

wherein administration of the anti-tumor composition causes less side effects than administration of a similar composition that does not contain shark cartilage extract.

9. An anti-tumor treatment kit comprising

a first composition comprising a pharmaceutical dosage of an anti-neoplastic agent; and

a second composition comprising a side effect-reducing amount of a shark cartilage extract.

10. The anti-tumor treatment kit of claim 9 , wherein the first composition and the second composition are each independently contained within a dosage form.

11. The anti-tumor treatment kit of claim 9 , wherein the anti-neoplastic agent is selected from the group consisting of busulfan, thiotepa, chlorambucil, cyclophosphamide, estramustine sodium phosphate, ifosfamide, mechlorethamine hydrochloride, melphalan, carmustine, lomustine, streptozocin, carboplatin, cisplatin, methotrexate sodium, cladribine, mercaptopurine, thioguanine, cytarabine, fluorouracil, hydroxyurea, daunorubicin, doxorubicin hydrochloride, epirubicin hydrochloride, idarubicin hydrochloride, dactinomycin, bleomycin sulfate, mitomycin, mitotane, mitoxantrone hydrochloride, etoposide, teniposide, docetaxel, paclitaxel, vinblastine sulfate, vincristine sulfate, vindesine sulfate, vinorelbine tartrate, altretamine, amsacrine, 1-asparaginase, dacarbazine, fludarabine phosphate, porfimer sodium, procarbazine hydrochloride, tretinoin (all-trans retinoic acid), marimastat, suramin, TNP 470, thalidomide and radiotherapeutics.

12. The anti-tumor treatment kit of claim 9 , wherein the anti-neoplastic agent is cisplatin.

13. The anti-tumor treatment kit of claim 9 , wherein the shark cartilage extract comprises water-soluble molecules, a major portion of which have a molecular weight of less than about 500 kDa.

14. The anti-tumor treatment kit of claim 9 , wherein the shark cartilage extract has been prepared by fractionating a crude shark cartilage extract comprising water soluble molecules obtained from shark cartilage material such that a major portion of the molecules having a molecular weight of greater than about 500 kDa is separated from a major portion of the molecules having a molecular weight of less than about 500 kDa.

15. The anti-tumor treatment kit of claim 9 , wherein the anti-neoplastic agent is present in a sub-optimal dosage amount and at least one of the first and second compositions further comprises a pharmaceutically acceptable carrier, wherein the pharmaceutically acceptable carrier is an aqueous solution, and administration of the compositions of the anti-tumor treatment kit causes less side effects than the administration of the compositions of a similar treatment kit that does not contain a composition containing shark cartilage extract.

16. The anti-tumor treatment kit of claim 9 , wherein at least one of the first and second compositions further comprises a pharmaceutically acceptable carrier, wherein said pharmaceutically acceptable carrier is an aqueous solution, the anti-neoplastic agent is present in an optimal dosage amount, and administration of the compositions of the anti-tumor treatment kit causes less side effects than the administration of the compositions of a similar treatment kit that does not contain shark cartilage extract.

17. The anti-tumor treatment kit of claim 9 , wherein the anti-neoplastic agent is cisplatin.

18. The anti-tumor treatment kit of claim 9 , wherein the first composition is contained within a parenteral dosage form and the second composition is contained within an oral dosage form.

Assignments (5)
CHANGE OF NAME Recorded Feb 28, 2006
From: LES LABORATOIRES AETERNA INC./AETERNA LABORATORIES INC.
To: AETERNA ZENTARIS INC.
Reel/Frame 017606/0311 →
RELEASE OF SECURITY INTEREST Recorded Feb 28, 2006
From: SGF SANTE INC.
To: AETERNA ZENTARIS INC.
Reel/Frame 017606/0606 →
SECURITY AGREEMENT Recorded Jun 11, 2003
From: LES LABORATOIRES AETERNA INC.
To: LE FONDS DE SOLIDARITE DES TRAVAILLEURS DU QUEBEC
Reel/Frame 014159/0082 →
SECURITY AGREEMENT Recorded Jun 11, 2003
From: LES LABORATORIES AETERNA INC.
To: SGF SANTE INC.
Reel/Frame 014159/0110 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2002
From: DUPONT, ERIC
To: LES LABORATOIRES AETERNA, INC.
Reel/Frame 013107/0878 →