IP Library Granted Patent US 7,812,163
Granted Patent B2
US 7,812,163 · App. 11/332,856 · Granted Oct 12, 2010

Methods and compositions for controlling ectoparasites

Assignee: HatchTech Pty Ltd.
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Quick Facts
Patent No.
US 7,812,163
App. No.
11/332,856
Granted
Oct 12, 2010
Kind
B2
Abstract

A method for inhibiting hatching of an ectoparasite egg, the method comprising exposing the ectoparasite egg to at least one metal chelating agent and/or metalloprotease inhibitor, wherein the metal chelating agent is a compound comprising at least two heteroatoms able to simultaneously coordinate with a metal ion, at least one of the two heteroatoms being selected from nitrogen, sulfur, oxygen and phosphorus, wherein the compound comprises at least one carbocyclic ring substituted with at least one heteroatom and/or with a substituent containing at least one heteroatom, or the compound comprises at least one heterocyclic ring containing at least one heteroatom, wherein said heterocyclic ring is optionally substituted with at least one heteroatom and/or with a substituent containing at least one heteroatom is provided. Methods of treating ectoparasite infestations and compositions for use in such methods are also provided.

Claims (31)

1. A method for inhibiting hatching of an ectoparasite egg comprising exposing the ectoparasite egg to a topical composition comprising at least one metal chelating agent wherein the at least one metal chelating agent is a compound of formula (Ia):

wherein X is a covalent bond, CH 2 —Z—CH 2 or —Z—

wherein R 1 and R 1′ are independently selected from hydrogen, or C 1-3 alkyl

wherein at least one of R 2 , R 2′ −, R 3 , R 3′ −, R 4 and R 4′ − is a methyl group and the remaining R 2 , R 2′ , R 3 , R 3′ , R 4 and R 4′ are independently selected from hydrogen or C 1-3 alkyl

Z is selected from a covalent bond, —NH—, —O—, —S—, —C(O)— and —C(S)—;

or a pharmaceutically, veterinary or agriculturally acceptable salt thereof.

2. A method according to claim 1 wherein Z is —NH—, —O— or S.

3. A method according to claim 1 wherein the compound of formula (Ia) is selected from:

6,6′-dimethyl-2,2′-dipyridyl,

5,5′-dimethyl-2,2′-dipyridyl,

4,4′-dimethyl-2,2′-dipyridyl,

or a pharmaceutically, veterinary or agriculturally acceptable salt thereof.

4. A method according to claim 1 , wherein the ectoparasite egg is laid by an ectoparasite of a species from an order selected from the group consisting of Lepidoptera, Hemiptera, Orthoptera, Psocoptera, Hymenoptera, Isoptera, Coleoptera, Dictyoptera, Thysanoptera, Homoptera, Diptera, Anaplura, Malophaga, Siphonaptera, Arachnida and Phthiraptera.

5. A method according to claim 4 , wherein the ectoparasite egg is laid by an ectoparasite of a species selected from the group consisting of Helicoverpa spp. Crocidolomia pavonana (Cabbage cluster caterpillar), Pieris rapae (Cabbage white butterfly), Phthorimaea operculella (Potatoe moth), Chrsyodexis spp. (Tobacco loopers), Plutella xylostella (Diamondback moth), Eiphyas postvittana (Walker)(light briown apple moth), Bovicola ovis (Sheep louse), Bovicola bovis, Haemotopinus eurysternus (short-nosed cattle louse), Linognathus vituli (long nosed cattle louse), Solenoptes scabiei suis, Sarcoptes scabiei bovis, Psoroptes ovis, Pthirus pubis, Pediculus humanus capitus, Pedicululs humanus humanus, Sarcoptes scabiei var, humani and Dermatophgoides spp.

6. A method of treating ectoparasite infestation in a host comprising topically applying to the host so that the ectoparasite egg on said host comes into topical contact with an effective amount of at least one metal chelating agent wherein the at least one metal chelating agent is a compound of formula (Ia):

wherein X is a covalent bond, CH 2 —Z—CH 2 or—Z—

wherein R 1 and R 1′ are independently selected from hydrogen, or C 1-3 alkyl

wherein at least one of R 2 , R 2′ −, R 3 , R 3′ −, R 4 and R 4′ − is a methyl group and the remaining R 2 , R 2 ′, R 3 , R 3 ′ , R 4 and R 4′ are independently selected from hydrogen or C 1-3 alkyl

Z is selected from a covalent bond, —NH—, —O—, —S—, —C(O)— and —C(S)—;

or a pharmaceutically, veterinary or agriculturally acceptable salt thereof.

7. A method according to claim 6 , wherein the host is a plant, an animal or a human.

8. A method of claim 6 wherein the ectoparasite infestation is caused by an ectoparasite of a species from an order selected from the group consisting of Lepidoptera, Hemiptera, Orthoptera, Psocoptera, Hymenoptera, Isoptera, Coleoptera, Dictyoptera, Thysanoptera, Homoptera, Diptera, Anaplura, Malophaga, Siphonaptera, Arachnida and Phthiraptera.

9. A method according to claim 6 , wherein the ectoparasite infestation is caused by an ectoparasite of a species from the group consisting Helicoverpa spp. Crocidolomia pavonana (Cabbage cluster caterpillar), Pieris rapae (Cabbage white butterfly), Phthorimaea operculella (Potatoe moth), Chrsyodexis spp. (Tobacco loopers), Plutella xylostella (Diamondback moth), Eiphyas postvittana (Walker)(light briown apple moth), Bovicola ovis (Sheep louse), Bovicola bovis, Haemotopinus eurysternus (short-nosed cattle louse), Linognathus vituli (long nosed cattle louse), Solenoptes scabiei suis, Sarcoptes scabiei bovis, Psoroptes ovis, Pthirus pubis, Pediculus humanus capitus, Pedicululs humanus humanus, Sarcoptes scabiei var, humani and Dermatophgoides spp.

10. A method according to claim 6 , wherein the ectoparasite infestation is a lice infestation.

11. A method according to claim 6 , wherein the metal chelating agent is applied simultaneously, separately or sequentially with a second ectoparasiticide.

12. A method according to claim 11 , wherein the second ectoparasiticide controls nymphs and/or adult ectoparasites.

13. A method according to claim 1 , wherein said composition is formulated for use in a direct topical application in a form selected from the group consisting of a dip, spray, aerosol, shampoo, mousse, emulsion, solution cream, dust, and lotion.

14. A method according to claim 6 , wherein said composition is formulated for use in a direct topical application in a form selected from the group consisting of a dip, spray, aerosol, shampoo, mousse, emulsion, solution cream, dust, and lotion.

15. A method according to claim 1 , wherein said ectoparasite egg is human head lice eggs and the composition is formulated for use in a topical application to human scalp and is in a form selected from the group consisting of a dip, spray, aerosol, shampoo, mousse, emulsion, solution cream, dust, and lotion.

16. A method according to claim 6 , wherein said ectoparasite egg is human head lice eggs and the composition is formulated for use in a topical application to human scalp and is in a form selected from the group consisting of a dip, spray, aerosol, shampoo, mousse, emulsion, solution cream, dust, and lotion.

17. A method according to any of claims 13 - 16 wherein said composition 5,5′-dimethyl-2,2′-dipyridyl.

Assignments (5)
SECURITY INTEREST Recorded Jan 30, 2026
From: CHANNEL PHARMACEUTICAL CORPORATION; PELTHOS THERAPEUTICS INC.
To: HORIZON TECHNOLOGY FINANCE CORPORATION
Reel/Frame 073644/0472 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 16, 2026
From: HATCHTECH PTY LTD
To: PELTHOS THERAPEUTICS INC.
Reel/Frame 074394/0060 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2024
From: DR. REDDY'S LABORATORIES, S.A.
To: HATCHTECH PTY LIMITED
Reel/Frame 067085/0376 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2016
From: HATCHTECH PTY LIMITED
To: DR. REDDY'S LABORATORIES, S.A.
Reel/Frame 039007/0287 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2006
From: BOWLES, VERNON MORRISON
To: HATCHTECH PTY LTD.
Reel/Frame 017512/0422 →
Priority Claims (1)
AU 2003903686 · Jul 16, 2003 · national
Continuity (4)
Continuation In Part PCTAU200400095500 · Jul 16, 2004
Provisional Application 6064582400 · Jan 20, 2005
Provisional Application 6048771700 · Jul 16, 2003
Related Publication 20060178404A1 · Aug 10, 2006