IP Library Patent Application 12180130
Patent Application
App. No. 12/180,130

USES OF TRIENTINE AND PENICILLAMINE AS COUNTERMEASURES TO METAL CONTAMINATION

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Patent No.
US None
App. No.
12/180,130
Abstract

Methods are provided for the alleviation, prevention and treatment of negative effects of overexposure to metal contaminants. Subjects exposed to a metal contaminant can be treated using trientine and/or penicillamine or salts, esters, solvates thereof. In addition, communities can protect its members by securing sufficient quantities of such countermeasures.

Claims (43)

1 . A method of treating a mammal suffering from one or more negative effects of overexposure to a metal contaminant comprising administering to the affected mammal a therapeutically effective amount of trientine or a pharmaceutically acceptable salt or solvate thereof, which metal contaminant includes at least one metal selected from the group consisting of a metal from Group IA, IIA, VIIB, VIIB, VIII, IB, IIB, IIIA, IVA, VA, VIA, Lanthanide Series, and Actinide Series of the periodic table, wherein said at least one metal is other than copper.

2 . The method of claim 1 wherein said at least one metal is selected from the group consisting of mercury, nickel, bismuth, palladium, zinc, cadmium, lead, cobalt, chromium, iron, silver, and cesium.

3 . The method of claim 1 wherein said at least one metal is palladium.

4 . The method of claim 1 wherein said at least one metal is cobalt.

5 . The method of claim 1 wherein said at least one metal is a radioactive isotope.

6 . The method of claim 2 wherein said at least one metal is a radioactive isotope.

7 . The method of claim 1 wherein said at least one metal is a radioactive isotope of a metal selected from the group consisting of americium, californium, cobalt, iridium, palladium, plutonium, polonium, and uranium.

8 . The method of claim 7 wherein said at least one metal is polonium.

9 . The method of claim 1 wherein said administration is carried out enterally.

10 . The method of claim 1 wherein said administration is carried out parenterally.

11 . The method of claim 1 wherein said trientine or a pharmaceutically acceptable salt or solvate thereof is administered in a dose ranging from about 4 mg of free base per kg of mammal per day to about 25 mg of free base per kg of mammal per day.

12 . The method of claim 1 wherein said administration is carried out sequentially or concomitantly with the administration of an effective amount of penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof.

13 . The method of claim 12 wherein said penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof is administered in a dose ranging from about 2 mg of penicillamine per kg of mammal per day to about 30 mg of penicillamine per kg of mammal per day.

14 . The method of claim 12 wherein the affected mammal is overexposed to at least two metals.

15 . The method of claim 14 wherein said at least two metals includes indium.

16 . The method of claim 12 wherein effective amounts of trientine hydrochloride and d-penicillamine are co-administered.

17 . A method of treating a community of individuals against the negative effects of overexposure to metal contamination on a large scale comprising providing a quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof sufficient to treat within a week or less of said overexposure every member of a community numbering between 5,000 and 1,000,000 individuals.

18 . The method of claim 17 wherein a quantity of dosage forms of penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof sufficient to treat within a week or less of said overexposure every member of a community numbering between 15,000 and 1,000,000 individuals is also provided.

19 . The method of claim 18 wherein said dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof and said dosage forms of penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof are provided in combined single dosage forms.

20 . The method of claim 17 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is provided sufficient to treat within three days or less of said overexposure every member of the community.

21 . The method of claim 17 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is provided sufficient to treat within two days or less of said overexposure every member of the community.

22 . The method of claim 17 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is provided sufficient to treat within one day or less of said overexposure every member of the community.

23 . The method of claim 17 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is provided sufficient to treat within a week or less of said overexposure every member of a community numbering between 15,000 and 1,000,000 individuals.

24 . The method of claim 17 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is provided sufficient to treat within a week or less of said overexposure every member of a community numbering between 100,000 and 1,000,000 individuals.

25 . The method of claim 17 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is provided sufficient to treat within a week or less of said overexposure every member of a community numbering between 500,000 and 1,000,000 individuals.

26 . A method of preparing a community against the negative effects of overexposure to metal contamination on a large scale comprising stockpiling a quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof sufficient to treat within a week or less of said overexposure every member of a community numbering between 5,000 and 1,000,000 individuals.

27 . The method of claim 26 wherein a quantity of dosage forms of penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof sufficient to treat within a week or less of said overexposure every member of a community numbering between 15,000 and 1,000,000 individuals is also stockpiled.

28 . The method of claim 27 wherein said dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof and said dosage forms of penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof are stockpiled in combined single dosage forms.

29 . The method of claim 26 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is stockpiled sufficient to treat within three days or less of said overexposure every member of the community.

30 . The method of claim 26 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is stockpiled sufficient to treat within two days or less of said overexposure every member of the community.

31 . The method of claim 26 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is stockpiled sufficient to treat within one day or less of said overexposure every member of the community.

32 . The method of claim 26 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is stockpiled sufficient to treat within a week or less of said overexposure every member of a community numbering between 15,000 and 1,000,000 individuals.

33 . The method of claim 26 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is stockpiled sufficient to treat within a week or less of said overexposure every member of a community numbering between 100,000 and 1,000,000 individuals.

34 . The method of claim 26 wherein said quantity of dosage forms of trientine or a pharmaceutically acceptable salt or solvate thereof is stockpiled sufficient to treat within a week or less of said overexposure every member of a community numbering between 500,000 and 1,000,000 individuals.

35 . The method of claim 12 wherein said trientine or a pharmaceutically acceptable salt or solvate thereof and said penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof are concomitantly administered in a single combination dosage form.

36 . A method of treating a mammal suffering from one or more negative effects of overexposure to a metal contaminant comprising sequentially or concomitantly administering to the affected mammal a therapeutically effective amount of trientine or a pharmaceutically acceptable salt or solvate thereof and penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof, which metal contaminant includes at least one radioactive isotope of a metal selected from the group consisting of americium, californium, cobalt, curium, iridium, palladium, plutonium, polonium, radium, strontium, and uranium.

37 . The method of claim 36 wherein the radioactive isotope is cobalt-60 or polonium-210 or a combination thereof.

38 . A pharmaceutical dosage form comprising an effective amount of trientine or its pharmaceutically acceptable salt or solvate and an effective amount of penicillamine or its pharmaceutically acceptable salt, ester or solvate and optionally one or more pharmaceutically acceptable carriers.

39 . A method of treating a mammal suffering from one or more negative effects of overexposure to polonium, comprising administering to the affected mammal a therapeutically effective amount of penicillamine or a pharmaceutically acceptable salt, ester, or solvate thereof.

40 . The method of claim 39 wherein said administration is carried out enterally.

41 . The method of claim 39 wherein said administration is carried out parenterally.

42 . The method of claim 39 wherein said penicillamine or a pharmaceutically acceptable salt or solvate thereof is administered in a dose ranging from about 2 mg of free base per kg of mammal per day to about 30 mg of free base per kg of mammal per day.

43 . The method of claim 14 wherein said at least two metals includes polonium.

Assignments (8)
RELEASE OF SECURITY INTEREST Recorded Apr 8, 2025
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: SOLTA MEDICAL, INC.; PRECISION DERMATOLOGY, INC.; BAUSCH HEALTH IRELAND LIMITED (F/K/A/ VALEANT PHARMACEUTICALS IRELAND LIMITED); SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD; SANTARUS, INC.; MEDICIS PHARMACEUTICAL CORPORATION; HUMAX PHARMACEUTICAL S.A.; SOLTA MEDICAL IRELAND LIMITED; BAUSCH & LOMB MEXICO, S.A. DE C.V.; BAUSCH+LOMB OPS B.V.; BAUSCH HEALTH AMERICAS, INC.; BAUSCH HEALTH COMPANIES INC.; BAUSCH HEALTH HOLDCO LIMITED; BAUSCH HEALTH MAGYARORSZAG KFT (A/K/A BAUSCH HEALTH HUNGARY LLC); BAUSCH HEALTH POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA (F/K/A VALEANT PHARMA POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA); BAUSCH HEALTH US, LLC; BAUSCH HEALTH, CANADA INC. / SANTE BAUSCH, CANADA INC.; ICN POLFA RZESZOW SPOLKA AKCYJNA (A/K/A ICN POLFA RZESZOW S.A.); ORAPHARMA, INC.; PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA SPOLKA AKCYJNA (A/K/A PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA S.A.); SOLTA MEDICAL DUTCH HOLDINGS B.V.; V-BAC HOLDING CORP.; VRX HOLDCO LLC; 1261229 B.C. LTD.; 1530065 B.C. LTD.
Reel/Frame 070778/0199 →
NOTICE OF SUCCESSION OF AGENCY Recorded Jan 9, 2015
From: GOLDMAN SACHS LENDING PARTNERS, LLC
To: BARCLAYS BANK PLC, AS SUCCESSOR AGENT
Reel/Frame 034749/0689 →
SECURITY AGREEMENT Recorded Jul 18, 2011
From: VALEANT PHARMACEUTICALS INTERNATIONAL, A DELAWARE CORPORATION; ATON PHARMA, INC., A DELAWARE CORPORATION; CORIA LABORATORIES, LTD., A DELAWARE CORPORATION; DOW PHARMACEUTICAL SCIENCES, INC., A DELAWARE CORPORATION; VALEANT PHARMACEUTICALS NORTH AMERICA LLC, A DELAWARE LLC; PRESTWICK PHARMACEUTICALS, INC., A DELAWARE CORPORATION; VALEANT BIOMEDICALS, INC., A DELAWARE CORPORATION
To: GOLDMAN SACHS LENDING PARTNERS LLC, AS COLLATERAL AGENT
Reel/Frame 026606/0061 →
PATENT SECURITY RELEASE AGREEMENT Recorded Mar 14, 2011
From: GOLDMAN SACHS LENDING PARTNERS LLC
To: VALEANT PHARMACEUTICALS INTERNATIONAL; VALEANT PHARMACEUTICALS NORTH AMERICA; CORIA LABORATORIES, LTD.; DOW PHARMACEUTICAL SCIENCES, INC.; ATON PHARMA, INC.
Reel/Frame 025950/0048 →
SECURITY AGREEMENT Recorded Oct 4, 2010
From: ATON PHARMA, INC.; VALEANT PHARMACEUTICALS NORTH AMERICA; VALEANT PHARMACEUTICALS INTERNATIONAL; CORIA LABORATORIES, LTD.; DOW PHARMACEUTICAL SCIENCES, INC.
To: GOLDMAN SACHS LENDING PARTNERS LLC, AS COLLATERAL AGENT
Reel/Frame 025084/0169 →
RELEASE OF SECURITY INTEREST IN PATENTS Recorded May 27, 2010
From: CIT HEALTHCARE LLC
To: ATON PHARMA, INC.
Reel/Frame 024445/0267 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2009
From: LEVINSON, BARRY; WELLS, MICHAEL
To: ATON PHARMA
Reel/Frame 022632/0743 →
SECURITY AGREEMENT Recorded Feb 19, 2009
From: ATON PHARMA, INC.
To: CIT HEALTHCARE LLC, AS AGENT
Reel/Frame 022283/0515 →