WO2005020995A1 - Methods related to the treatment of mucosal associated conditions - Google Patents
Methods related to the treatment of mucosal associated conditions Download PDFInfo
- Publication number
- WO2005020995A1 WO2005020995A1 PCT/US2004/028407 US2004028407W WO2005020995A1 WO 2005020995 A1 WO2005020995 A1 WO 2005020995A1 US 2004028407 W US2004028407 W US 2004028407W WO 2005020995 A1 WO2005020995 A1 WO 2005020995A1
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- WO
- WIPO (PCT)
- Prior art keywords
- amines
- erm
- mucosal surface
- irm
- substituted
- Prior art date
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0034—Urogenital system, e.g. vagina, uterus, cervix, penis, scrotum, urethra, bladder; Personal lubricants
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/02—Drugs for genital or sexual disorders; Contraceptives for disorders of the vagina
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Definitions
- the specified delivery time for the application of an IRM to a mucosal surface may be six hours or less, four hours or less, two hours or less, or one hour or less, depending on the desired treatment regimen.
- the specified delivery time for the application of an ERM to a mucosal surface may be even shorter. For example, it can be sixty minutes or less, thirty minutes or less, or even twenty minutes or less.
- the specified delivery time is at least ten minutes, and preferably at least fifteen minutes for desired effect.
- an IRM may be applied once a week.
- an IRM may also be applied several times a week. For example, an IRM may be applied twice a week, three times a week, or five times a week.
- a "mucosal surface” includes mucosal membranes such as buccal, gingival, nasal, ocular, tracheal, bronchial, gastrointestinal, rectal, urethral, ureteral, vaginal, cervical, and uterine mucosal membranes.
- mucosal membranes such as buccal, gingival, nasal, ocular, tracheal, bronchial, gastrointestinal, rectal, urethral, ureteral, vaginal, cervical, and uterine mucosal membranes.
- the therapeutic affect of the IRM may extend only to the superficial layers of the mucosal surface or to tissues deep below the surface.
- Immune response modifiers useful in the methods ofthe present invention include compounds that act on the immune system by inducing and/or suppressing cytokine biosynthesis. IRMs possess potent immunostimulating activity including, but not limited to, antiviral and antitumor activity, and can also down-regulate other aspects ofthe immune response, for example, shifting the immune response away from a TH-2 immune response, which is useful for treating a wide range of TH-2 mediated diseases. IRMs can also be used to modulate humoral immunity by stimulating antibody production by B cells. Further, various IRMs have been shown to be useful as vaccine adjuvants (see, e.g., U.S. Pat. Nos.
- the methods of the present invention do not use imiquimod or resiquimod.
- the immune response modifier is selected from the group consisting of imidazoquinoline amines, tetrahydro imidazoquinoline amines, imidazopyridine amines, 6,7-fused cycloalkylimidazopyridine amines, 1,2-bridged imidazoquinoline amines, imidazonaphthyridine amines, imidazotetrahydronaphthyridine amines, oxazoloquinoline amines, thiazoloquinoline amines, oxazolopyridine amines, thiazolopyridine amines, oxazolonaphthyridine amines, thiazolonaphthyridine amines, IH- imidazo dimers fused to pyridine amines, quinoline amines, tetrahydroquinoline amines, imidazopyr
- IRMs diseases for which IRMs may be used as treatments include, but are not limited to: viral diseases, such as genital warts, common warts, plantar warts, hepatitis B, hepatitis C, herpes simplex virus type I and type II, molluscum contagiosum, variola, HIV, CMV, VZV, rhino virus, adenovirus, coronavirus, influenza, para-influenza; bacterial diseases, such as tuberculosis, and mycobacterium avium, leprosy; other infectious diseases, such as fungal diseases, chlamydia, Candida, aspergillus, cryptococcal meningitis, pneumocystis carnii, cryptosporidiosis, histoplasmosis, toxoplasmosis, trypanosome infection, leishmaniasis; neoplastic diseases, such as intraepithelial neoplasias, cervical dysplasia, actin
- Example 2 Devices were prepared as described in Example 1 and saturated with either a solution containing 1.0 % by weight of ERM 1 in isostearic acid or with a solution containing 0.1 % by weight of ERM 1 in isostearic acid. Rats were dosed intravaginally; the devices were removed after 2 hours. Cytokines were assayed at 2, 4, and 6 hours post dosing. A group of rats that did not receive any treatment served as controls. The results are shown in the table below where each value is the mean ofthe values for 3 rats.
- Example 7 Devices were prepared from cotton pellets as described in Example 6. The devices were saturated with one ofthe following solutions: 5.0 % ERM 3 in 50/50 ISA/EPM; 5.0 % IRM 7 in 50/50 ISA/EPM; 5.0 % ERM 9 in 50/50 ISA/EPM; 5.0% IRM 10 in 50/50 ISA/EPM; or with 50/50 ISA/EPM (vehicle). Rats were dosed intravaginally; the devices were removed after 2 hours. Cytokines were assayed at 2, 4, and 6 hours post dosing. The results are shown in the table below where each value is the mean ofthe values for 6 rats.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Gynecology & Obstetrics (AREA)
- Tropical Medicine & Parasitology (AREA)
- Reproductive Health (AREA)
- Biotechnology (AREA)
- Urology & Nephrology (AREA)
- AIDS & HIV (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
- Absorbent Articles And Supports Therefor (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2004268665A AU2004268665A1 (en) | 2003-09-02 | 2004-09-01 | Methods related to the treatment of mucosal associated conditions |
| EP04782823A EP1663222A4 (en) | 2003-09-02 | 2004-09-01 | METHODS RELATING TO THE TREATMENT OF GIANCES |
| JP2006524955A JP2007504172A (ja) | 2003-09-02 | 2004-09-01 | 粘膜に関連した症状の処置に関する方法 |
| CA002536578A CA2536578A1 (en) | 2003-09-02 | 2004-09-01 | Methods related to the treatment of mucosal associated conditions |
| MXPA06002408A MXPA06002408A (es) | 2003-09-02 | 2004-09-01 | Metodos relacionados al tratamiento de condiciones asociadas a la mucosa. |
| US10/595,117 US20060216333A1 (en) | 2003-09-02 | 2004-09-01 | Methods related to the treatment of mucosal associated conditions |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49960703P | 2003-09-02 | 2003-09-02 | |
| US60/499,607 | 2003-09-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2005020995A1 true WO2005020995A1 (en) | 2005-03-10 |
Family
ID=34272845
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2004/028407 Ceased WO2005020995A1 (en) | 2003-09-02 | 2004-09-01 | Methods related to the treatment of mucosal associated conditions |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20060216333A1 (https=) |
| EP (1) | EP1663222A4 (https=) |
| JP (1) | JP2007504172A (https=) |
| CN (1) | CN1845736A (https=) |
| AU (1) | AU2004268665A1 (https=) |
| CA (1) | CA2536578A1 (https=) |
| MX (1) | MXPA06002408A (https=) |
| WO (1) | WO2005020995A1 (https=) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006115413A3 (en) * | 2005-04-27 | 2007-04-19 | Univ Leiden Medical Ct | Methods and means for the treatment of hpv induced intraepithelial neoplasias |
| EP1889609A3 (en) * | 2006-07-18 | 2008-08-13 | Meda AB | Immune response modifier foam formulations |
| US7655672B2 (en) | 2004-12-17 | 2010-02-02 | 3M Innovative Properties Company | Immune response modifier formulations containing oleic acid and methods |
| US8124096B2 (en) | 2006-07-31 | 2012-02-28 | 3M Innovative Properties Company | Immune response modifier compositions and methods |
| US8889154B2 (en) | 2005-09-15 | 2014-11-18 | Medicis Pharmaceutical Corporation | Packaging for 1-(2-methylpropyl)-1H-imidazo[4,5-c] quinolin-4-amine-containing formulation |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040265351A1 (en) | 2003-04-10 | 2004-12-30 | Miller Richard L. | Methods and compositions for enhancing immune response |
| AU2004268625B2 (en) | 2003-08-27 | 2011-03-31 | 3M Innovative Properties Company | Aryloxy and arylalkyleneoxy substituted imidazoquinolines |
| KR20060120069A (ko) | 2003-10-03 | 2006-11-24 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 피라졸로피리딘 및 그의 유사체 |
| AR046046A1 (es) | 2003-10-03 | 2005-11-23 | 3M Innovative Properties Co | Imidazoquinolinas alcoxi sustituidas. composiciones farmaceuticas. |
| CA2547020C (en) | 2003-11-25 | 2014-03-25 | 3M Innovative Properties Company | 1h-imidazo[4,5-c]pyridine-4-amine derivatives as immune response modifier |
| US8541438B2 (en) | 2004-06-18 | 2013-09-24 | 3M Innovative Properties Company | Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines |
| JP5543068B2 (ja) | 2004-12-30 | 2014-07-09 | スリーエム イノベイティブ プロパティズ カンパニー | キラル縮合[1,2]イミダゾ[4,5−c]環状化合物 |
| EP1831221B1 (en) | 2004-12-30 | 2012-08-08 | 3M Innovative Properties Company | Substituted chiral fused 1,2 imidazo 4,5-c ring compounds |
| US8378102B2 (en) | 2005-02-09 | 2013-02-19 | 3M Innovative Properties Company | Oxime and hydroxylamine substituted thiazolo[4,5-c] ring compounds and methods |
| AU2006212765B2 (en) | 2005-02-09 | 2012-02-02 | 3M Innovative Properties Company | Alkyloxy substituted thiazoloquinolines and thiazolonaphthyridines |
| EP1845988A2 (en) | 2005-02-11 | 2007-10-24 | 3M Innovative Properties Company | Substituted imidazoquinolines and imidazonaphthyridines |
| JP2008531567A (ja) | 2005-02-23 | 2008-08-14 | コーリー ファーマシューティカル グループ,インコーポレイテッド | ヒドロキシアルキル置換イミダゾキノリン化合物および方法 |
| EP1851224A2 (en) | 2005-02-23 | 2007-11-07 | 3M Innovative Properties Company | Hydroxyalkyl substituted imidazoquinolines |
| EP1851220A2 (en) | 2005-02-23 | 2007-11-07 | 3M Innovative Properties Company | Hydroxyalkyl substituted imidazonaphthyridines |
| AU2006216686A1 (en) | 2005-02-23 | 2006-08-31 | Coley Pharmaceutical Group, Inc. | Method of preferentially inducing the biosynthesis of interferon |
| ZA200803029B (en) | 2005-09-09 | 2009-02-25 | Coley Pharm Group Inc | Amide and carbamate derivatives of alkyl substituted /V-[4-(4-amino-1H-imidazo[4,5-c] quinolin-1-yl)butyl] methane-sulfonamides and methods |
| EA200800782A1 (ru) | 2005-09-09 | 2008-08-29 | Коли Фармасьютикал Груп, Инк. | ПРОИЗВОДНЫЕ АМИДА И КАРБАМАТА N-{2-[4-АМИНО-2-(ЭТОКСИМЕТИЛ)-1Н-ИМИДАЗОЛО[4,5-c]ХИНОЛИН-1-IL]-1,1-ДИМЕТИЛЭТИЛ}МЕТАНСУЛЬФОНАМИДА И СПОСОБЫ |
| KR20080083270A (ko) | 2005-11-04 | 2008-09-17 | 콜레이 파마시티컬 그룹, 인코포레이티드 | 하이드록시 및 알콕시 치환된 1에이치 이미다조퀴놀린 및방법 |
| EP1988896A4 (en) | 2006-02-22 | 2011-07-27 | 3M Innovative Properties Co | CONJUGATES TO MODIFY IMMUNE REACTIONS |
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Also Published As
| Publication number | Publication date |
|---|---|
| AU2004268665A1 (en) | 2005-03-10 |
| CA2536578A1 (en) | 2005-03-10 |
| EP1663222A4 (en) | 2008-05-21 |
| EP1663222A1 (en) | 2006-06-07 |
| CN1845736A (zh) | 2006-10-11 |
| MXPA06002408A (es) | 2006-06-20 |
| JP2007504172A (ja) | 2007-03-01 |
| US20060216333A1 (en) | 2006-09-28 |
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