US2007141044A1PendingUtilityA1
Method for treating cancer patients undergoing chemotherapy
Individually held — no corporate assignee on recordPriority: Jun 5, 2003Filed: Jun 4, 2004Published: Jun 21, 2007
Est. expiryJun 5, 2023(expired)· nominal 20-yr term from priority
Inventors:Shalom Z. Hirschman
A61K 31/00A61K 38/012A61K 31/7105A61K 45/06A61P 7/00A61P 35/00A61P 7/06A61P 43/00A61K 38/01A61K 38/16
61
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Claims
Abstract
A method for treating cancer patients undergoing chemotherapeutic treatments by administering Product R, a peptide-nucleic acid preparation, is disclosed.
Claims
exact text as granted — not AI-modified1 . A method of maintaining or increasing the number of white blood cells in a cancer patient undergoing chemotherapeutic treatment for cancer, comprising administering to said patient an effective treatment amount of Product R.
2 . The method of claim 1 in which said cancer patient does not have basal cell carcinoma or a cancer of a lymphocytic cell.
3 . The method of claim 1 or 2 in which said administering is not subcutaneous, intralesional, topical or by injection.
4 . The method of claim 1 in which said administering to said patient is parenterally and said Product R is in a sterile injectable formulation.
5 . The method of claim 4 in which said cancer patient does not have basal cell carcinoma or a cancer of a lymphocytic cell.
6 . The method of claim 1 in which an effective treatment amount of Product R is in a range from about 5 microliters to about 40 microliters per kilogram of body weight per day in a sterile formulation.
7 . The method of claim 1 in which an effective treatment amount of Product R is in a range from about 10 microliters to about 25 microliters per kilogram of body weight per day in a sterile formulation.
8 . The method of claim 1 in which an effective treatment amount of Product R is about 30 microliters per kilogram of body weight per day in a sterile injectable formulation for about one week, followed by about 15 microliters per kilogram of body weight per day in a sterile formulation.
9 . A method of maintaining or increasing the number of platelets in the blood in a cancer patient undergoing chemotherapeutic treatment for cancer, comprising administering to said patient an effective treatment amount of Product R.
10 . The method of claim 9 in which said cancer patient does not have basal cell carcinoma or a cancer of a lymphocytic cell.
11 . The method of claim 9 or 10 in which said administering is not subcutaneous, intralesional, topical or by injection.
12 . The method of claim 9 in which said administering to said patient is parenterally and said Product R is in a sterile injectable formulation.
13 . The method of claim 12 in which said cancer patient does not have basal cell carcinoma or a cancer of a lymphocytic cell.
14 . The method of claim 9 in which an effective treatment amount of Product R is in a range from about 5 microliters to about 40 microliters per kilogram of body weight per day in a sterile formulation.
15 . The method of claim 9 in which an effective treatment amount of Product R is in a range from about 10 microliters to about 25 microliters per kilogram of body weight per day in a sterile formulation.
16 . The method of claim 9 in which an effective treatment amount of Product R is about 30 microliters per kilogram of body weight per day in a sterile injectable formulation for about one week, followed by about 15 microliters per kilogram of body weight per day in a sterile formulation.
17 . A method of reducing gastric-intestinal toxicity in a cancer patient resulting from an anti-cancer chemotherapeutic agent comprising administering to said patient an effective treatment amount of Product R.
18 . The method of claim 17 in which said cancer patient does not have basal cell carcinoma or a cancer of a lymphocytic cell.
19 . The method of claim 17 or 18 in which said administering is not subcutaneous, intralesional, topical or by injection.
20 . The method of claim 17 in which said administering to said patient is parenterally and said Product R is in a sterile injectable formulation.
21 . The method of claim 20 in which said cancer patient does not have basal cell carcinoma or a cancer of a lymphocytic cell.
22 . The method of claim 17 in which an effective treatment amount of Product R is in a range from about 5 microliters to about 40 microliters per kilogram of body weight per day in a sterile formulation.
23 . The method of claim 17 in which an effective treatment amount of Product R is in a range from about 10 microliters to about 25 microliters per kilogram of body weight per day in a sterile formulation.
24 . The method of claim 17 in which an effective treatment amount of Product R is about 30 microliters per kilogram of body weight per day in a sterile injectable formulation for about one week, followed by about 15 microliters per kilogram of body weight per day in a sterile formulation.
25 . A pharmaceutical composition comprising an effective treatment amount of Product R, an anti-cancer chemotherapeutic agent, and a pharmaceutically acceptable carrier
26 . A kit comprising a first container which contains an effective treatment amount of Product R; and a second container which contains an anti-cancer chemotherapeutic agent.
27 . The kit of claim 26 further comprising a needle or syringe.Join the waitlist — get patent alerts
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