Classifications

• • 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
  • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
  • A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
• • 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
  • A61K9/007—Pulmonary tract; Aromatherapy
  • A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
  • A61K9/0075—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
• • 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
  • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
  • A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • 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
• • 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
  • A61P11/06—Antiasthmatics
• • 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
  • A61P11/08—Bronchodilators
• • 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
  • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
  • A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
  • A61K9/145—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic compounds

Definitions

• the present invention relates to use of a composition for symptomatic relief, when needed, comprising, in admixture
• the invention further relates to a method for prevention or treatment of an acute condition of asthma and/or intermittent asthma and/or episodes in chronic asthma by administering, by inhalation, a composition comprising the first and second active ingredients as defined previously.
• asthma Despite recent advances in the awareness of asthma and the introduction of powerful and effective anti-asthma drugs, asthma remains a poorly understood and frequently poorly treated disease. There have been recent advances in the treatment of the disease which result from the recognition that asthma is a chronic inflammatory disease. Therapy is now aimed at both controlling the symptoms and reducing the inflammation. The symptoms may be controlled by ⁇ 2 -adrenoceptor agonists such as terbutaline, salbutamol, formoterol and salmeterol. Prophylactic therapy is typically provided by steroids such asbeclomethasone dipropionate, fluticasone propionate, mometasone furoate and budesonide.
• steroids such asbeclomethasone dipropionate, fluticasone propionate, mometasone furoate and budesonide.
• composition for symptomatic relief when needed comprising, in admixture
• a second active ingredient which is budesonide for the manufacture of a medicament for use in the prevention or treatment of an acute condition of asthma and/or intermittent asthma and/or episodes in chronic asthma.
• composition when needed, relates to use of said composition during one or more of the following conditions:
• Acute asthma attacks may occur on an irregular basis when exposed to an agent e.g. during the pollen season, a virus infection, cold air, perfumes or any other agent(s) triggering an asthma attack in the patient.
• compositions comprising active compounds (a) and (b) for treating acute conditions of asthma, intermittent asthma and episodes in chronic asthma, in addition to treating chronic asthma on a regular basis, with the same active compounds (a) and (b) or one or more different active compounds, preferably selected from short-acting ⁇ -agonists, long-acting ⁇ -agonists and glucocorticosteroids.
• a method of prevention or treatment of an acute condition of asthma and/or intermittent asthma and/or episodes in chronic asthma, when needed which comprises administering, by inhalation, to a patient an effective amount of a composition comprising, in admixture:
• the medicament can be administered when needed to a patient with an acute attack of asthma.
• the combination of formoterol and budesonide can be used as a rescue medication. Worsening of symptoms can be counteracted by incremental use of the combination for symptom relief, e.g. during exacerbations with the additional steroid component coming in as early as possible to suppress the enhanced airway inflammation.
• the long duration of formoterol will reduce the risk of too frequent dosing.
• When taking the combination budesonide/formoterol when needed the severity of exacerbations can be reduced.
• the as needed use (Pro Re Nata, PRN) will also minimize the difficulty of predicting which patients will be controlled on a low dose of inhaled steroid rather than increasing the steroid dose before adding a long-acting ⁇ 2 -agonist.
• Under-treatment with inhaled glucocorticosteroids following a too low maintenance dose will be more or less “selfcorrected” by the rescue usage according to the present invention.
• the PRN use of the combination will always give some beneficial anti-inflammatory effects even if it is used by the patient only for rescue purposes.
• a treatment for patients suffering from respiratory disease, particularly asthma will therefore be to use the combination formoterol/budesonide for maintenance therapy as well as on an as needed basis (for rescue purposes). e.g. for prevention of exercise and/or allergen induced asthma.
• Formoterol is a compound which can exist in several stereochemical forms.
• the present invention includes the individual stereoisomers as well as mixtures thereof. It is intended that the present invention includes geometrical isomers, rotational isomers. racemates, diastereomers and enantiomers. in particular the R,R enantiomer of formoterol.
• Suitable physiologically salts of formoterol include acid addition salts derived from inorganic and organic acids such as the hydrochloride. hydrobronide, sulfate, phosphate. maleate, fumarate, tartrate, citrate. benzoate, 4-methoxybenzoate, 2- or 4-hydroxybenzoate, 4-chlorobenzoate, p-toluenesulphonate, methanesulphonate, ascorbate, salicylate, acetate. succinate, lactate, glutarate, gluconate, tricarballylate, hydroxy-naphthalene-carboxylate or oleate.
• Formoterol is preferably used in the form of its fumarate salt and as a dihydrate of this salt.
• compositions comprising the 22 R epimer of budesonide as the second active ingredient.
• a suitable unit dose of formoterol (as fumarate dihydrate) is in the range of from 1 ⁇ g to 48 ⁇ g, preferably from 2 ⁇ g to 24 ⁇ g, and more preferably between 3 ⁇ g and 12 ⁇ g.
• the daily dose of formoterol (as fumarate dihydrate), including maintenance therapy, should be in the range of from 1 ⁇ g to 100 ⁇ g, preferably from 2 ⁇ g to 60 ⁇ g, and more preferably from 3 ⁇ g to of 48 ⁇ g.
• a suitable unit dose of budesonide is in the range of from 20 ⁇ g to 1600 ⁇ g, suitably from 30 ⁇ g to 800 ⁇ g, preferably from 50 ⁇ g to 400 ⁇ g, and more preferably between 100 ⁇ g and 200 ⁇ g.
• the daily dose of budesonide, including maintenance therapy, should be in the range of 20 ⁇ g to 4800 ⁇ g, preferably from 30 ⁇ g to 3200 ⁇ g, and more preferably from 40 ⁇ g to 1600 ⁇ g.
• the particular dose regimen will depend on the patient (age, sex, weight etc.) and the severity of the disease (mild, moderate, severe asthma etc.).
• the molar ratio of the first active ingredient (as formoterol) to the second active ingredient of the invention suitably lies in the range of from 1:1 to 1:100, preferably from 1:1 to 1:70, and more preferably from 1:1 to 1:50.
• the mixture comprises one or more pharmaceutically acceptable additives, diluents or carriers, more preferably in an amount of from 50 ⁇ g to 4000 ⁇ g in each dose, most preferably in an amount of from 100 ⁇ g to 2000 ⁇ g and most preferably from 100 ⁇ g to 1000 ⁇ g.
• suitable additives, diluents or carriers include lactose, dextran, mannitol or glucose.
• lactose is used, and more preferably as the monohydrate.
• One or more of the ingredients of the mixture may be in the form of dry powder, more preferably a small particle dry powder, most preferably an agglomerated small particle dry powder.
• one or more of the active ingredients (a) or (b) are in the form of an ordered mixture with diluent, additive or carrier.
• the ingredients used in the invention can be obtained in these preferred forms using methods known to those skilled in the art.
• the particle size of the active ingredients is preferably less than 10 ⁇ m.
• Administration may be by inhalation orally or intranasally.
• the ingredients of the system are preferably adapted to be administered from a dry powder inhaler, a pressurized metered dose inhaler, or a nebulizer.
• the ingredients of the system are preferably in a small particle form. They are dissolved, or, preferably, suspended in a liquid propellant mixture.
• the propellants which can be used include chlorofluorocarbons, hydrocarbons or hydrofluorocarbons.
• Especially preferred propellants are P134a (tetrafluoroethane), P152a (difluoroethane) and P227 (heptafluropropane) each of which may be used alone or in combination. They are optionally used in combination with one or more other propellants and/or one or more surfactants and/or one or more other excipients, for example ethanol, a lubricant, an antioxidant and/or a stabilizing agent.
• ingredients of the system of the invention are adapted to be administered via a nebulizer they may be in the form of a nebulized aqueous suspension or solution, with or without suitable pH or tonicity adjustment, either as a unit dose or multidose formulation.
• micronization is carried out in a conventional manner such that the particle size range for each component is suitable for administration by inhalation.
• Turbuhaler is a trademark of Astra AB.
• a patient on maintenance treatment with the fixed combination formoterol fumarate dihydrate/budesonide in a dose of 4.5/80 ⁇ g or 4.5/160 ⁇ g bid additionally uses the same combination either for rescue purposes once or twice daily to treat sporadic breakthrough symptoms, or as needed to treat exacerbations during one or two weeks, with a maximum daily dose of 36/640 ⁇ g (8 puffs of 4.5/80 ⁇ g) and 36/1280 ⁇ g (8 puffs of 4.5/160 ⁇ g), respectively.
• a patient with intermittent asthma uses the fixed combination formoterol fumarate dihydrate/budesonide as sole medication to be taken as needed until the asthma resolves.
• the highest recommended daily dose will be either 36/640 ⁇ g (8 puffs of 4.5/80 ⁇ g) or 36/1280 ⁇ g (8 puffs of 4.5/160 ⁇ g) for a period not exceeding 8-120 weeks. If symptoms still persist after that period of time—regular maintenance therapy should be considered.

Landscapes

• Health & Medical Sciences (AREA)
• Veterinary Medicine (AREA)
• General Health & Medical Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Pharmacology & Pharmacy (AREA)
• Medicinal Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Public Health (AREA)
• Animal Behavior & Ethology (AREA)
• Epidemiology (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Engineering & Computer Science (AREA)
• Pulmonology (AREA)
• General Chemical & Material Sciences (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Otolaryngology (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Medicinal Preparation (AREA)

Priority Applications (1)

Applications Claiming Priority (2)

Related Parent Applications (1)

Related Child Applications (1)

Publications (1)

Family

ID=20411658

Family Applications (2)

Family Applications After (1)

Country Status (35)

Cited By (6)

Families Citing this family (38)

Citations (8)

Family Cites Families (29)

• 1998
  • 1998-06-11 SE SE9802073A patent/SE9802073D0/xx unknown
• 1999
  • 1999-05-28 AR ARP990102532A patent/AR018410A1/es unknown
  • 1999-06-01 TW TW088109070A patent/TWI252756B/zh not_active IP Right Cessation
  • 1999-06-09 SA SA99200234A patent/SA99200234B1/ar unknown
  • 1999-06-09 MY MYPI99002351A patent/MY129281A/en unknown
  • 1999-06-10 ID IDW20002566A patent/ID27937A/id unknown
  • 1999-06-10 BR BR9911073-3A patent/BR9911073A/pt not_active Application Discontinuation
  • 1999-06-10 UA UA2000126983A patent/UA87956C2/uk unknown
  • 1999-06-10 CA CA002334411A patent/CA2334411C/en not_active Expired - Lifetime
  • 1999-06-10 HU HU0103108A patent/HUP0103108A3/hu unknown
  • 1999-06-10 CZ CZ20004593A patent/CZ300874B6/cs not_active IP Right Cessation
  • 1999-06-10 TR TR2000/03666T patent/TR200003666T2/xx unknown
  • 1999-06-10 PT PT99930103T patent/PT1085877E/pt unknown
  • 1999-06-10 ES ES99930103T patent/ES2302384T3/es not_active Expired - Lifetime
  • 1999-06-10 DE DE69938390T patent/DE69938390T2/de not_active Expired - Lifetime
  • 1999-06-10 JP JP2000553082A patent/JP2002517450A/ja active Pending
  • 1999-06-10 IL IL13992199A patent/IL139921A0/xx active IP Right Grant
  • 1999-06-10 US US09/367,950 patent/US20010049396A1/en not_active Abandoned
  • 1999-06-10 EP EP99930103A patent/EP1085877B1/en not_active Revoked
  • 1999-06-10 NZ NZ536279A patent/NZ536279A/en not_active IP Right Cessation
  • 1999-06-10 KR KR1020007013993A patent/KR20010052721A/ko not_active Application Discontinuation
  • 1999-06-10 PL PL99344665A patent/PL344665A1/xx unknown
  • 1999-06-10 AT AT99930103T patent/ATE389409T1/de active
  • 1999-06-10 DK DK99930103T patent/DK1085877T3/da active
  • 1999-06-10 EP EP10178172A patent/EP2266574A1/en not_active Withdrawn
  • 1999-06-10 SK SK1888-2000A patent/SK286252B6/sk not_active IP Right Cessation
  • 1999-06-10 CN CNB998072303A patent/CN100389771C/zh not_active Expired - Lifetime
  • 1999-06-10 EP EP03002381A patent/EP1316311A1/en not_active Withdrawn
  • 1999-06-10 RU RU2000131218/14A patent/RU2222332C2/ru not_active IP Right Cessation
  • 1999-06-10 WO PCT/SE1999/001031 patent/WO1999064014A1/en not_active Application Discontinuation
  • 1999-06-10 AU AU46710/99A patent/AU771715B2/en not_active Expired
  • 1999-06-10 EE EEP200000740A patent/EE05661B1/xx unknown
• 2000
  • 2000-11-27 IL IL139921A patent/IL139921A/en not_active IP Right Cessation
  • 2000-11-27 ZA ZA200006943A patent/ZA200006943B/en unknown
  • 2000-12-05 IS IS5752A patent/IS5752A/is unknown
  • 2000-12-08 NO NO20006253A patent/NO20006253L/no not_active Application Discontinuation
• 2001
  • 2001-08-17 HK HK01105814A patent/HK1035145A1/xx not_active IP Right Cessation
• 2003
  • 2003-09-19 US US10/665,240 patent/US9295644B2/en not_active Expired - Lifetime
• 2008
  • 2008-05-13 CY CY20081100507T patent/CY1110376T1/el unknown
• 2013
  • 2013-02-18 NO NO20130269A patent/NO20130269L/no not_active Application Discontinuation
• 2014
  • 2014-06-27 NO NO20140823A patent/NO20140823L/no not_active Application Discontinuation

Patent Citations (9)

Also Published As

Similar Documents

Legal Events