US20090304604A1 - Pulmonary delivery of alpha-1 proteinase inhibitor - Google Patents

Pulmonary delivery of alpha-1 proteinase inhibitor Download PDF

Info

Publication number
US20090304604A1
US20090304604A1 US12/278,767 US27876707A US2009304604A1 US 20090304604 A1 US20090304604 A1 US 20090304604A1 US 27876707 A US27876707 A US 27876707A US 2009304604 A1 US2009304604 A1 US 2009304604A1
Authority
US
United States
Prior art keywords
api
aerosol
purified
pulmonary
proteinase inhibitor
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/278,767
Other languages
English (en)
Inventor
Shabtai Bauer
Manfred Keller
Martin Knoch
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
PARI Pharma GmbH
Kamada Ltd
Original Assignee
PARI Pharma GmbH
Kamada Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by PARI Pharma GmbH, Kamada Ltd filed Critical PARI Pharma GmbH
Priority to US12/278,767 priority Critical patent/US20090304604A1/en
Assigned to KAMADA LTD. reassignment KAMADA LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BAUER, SHABTAI
Assigned to PARI PHARMA GMBH reassignment PARI PHARMA GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KELLER, MANFRED, KNOCH, MARTIN
Publication of US20090304604A1 publication Critical patent/US20090304604A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/55—Protease inhibitors
    • A61K38/57—Protease inhibitors from animals; from humans
    • 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
    • A61K9/0078—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a nebulizer such as a jet nebulizer, ultrasonic nebulizer, e.g. in the form of aqueous drug solutions or dispersions
    • 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

Definitions

  • the present invention relates to a system and methods of treating pulmonary diseases comprising the administration of a ready-to-use liquid composition comprising alpha-1 proteinase inhibitor (API) in aerosol form in a nebulizer.
  • API compositions are adapted to optimize the delivery of the active ingredient to the lungs.
  • Alpha-1 proteinase inhibitor also known as Alpha-1-antitrypsin (A1AT, AAT) and Serine protease inhibitor
  • A1AT Alpha-1-antitrypsin
  • Serine protease inhibitor is a plasma-derived protein belonging to the family of serine proteinase inhibitors. It is a glycoprotein having an average molecular weight of 50,600 daltons, produced by the liver and secreted into the circulatory system. The protein is a single polypeptide chain, to which several oligosaccharide units are covalently bound.
  • API has a role in controlling tissue destruction by endogenous serine proteinases, and is the most prevalent serine proteinase inhibitor in blood plasma. API inhibits, inter alia, trypsin, chymotrypsin, various types of elastases, skin collagenase, renin, urokinase and proteases of polymorphonuclear lymphocytes.
  • API is currently used therapeutically for the treatment of pulmonary emphysema in patients who have a genetic API deficiency, also known as Alpha-1 Antitrypsin Deficiency or Congenital Emphysema.
  • Purified API has been approved for replacement therapy (also known as “augmentation therapy”) in these patients.
  • the endogenous role of API is to regulate the activity of neutrophil elastase, which breaks down foreign proteins present in the lung. In the absence of sufficient quantities of API, the elastase breaks down lung tissue, which over time results in chronic lung tissue damage and emphysema.
  • API has also been proposed as a treatment for cystic fibrosis (CF) patients who suffer from recurrent endobronchial infections and sinusitis.
  • CF cystic fibrosis
  • the major cause of morbidity and mortality among CF patients is lung diseases.
  • CF patients carry a mutation in the CFTR gene, resulting in a malfunctioning CTFR protein, defective water and salt transport and the ensuing thick secretions in the lung.
  • the membrane defect caused by the CFTR mutation leads to chronic lung inflammation and infection.
  • elastase secreted by neutrophils in response to infection is neutralized by API.
  • API is known to penetrate into pulmonary tissue and exert its activity within this tissue.
  • the unregulated inflammatory response overwhelms the normal protease (elastase)/antiprotease (API) balance.
  • the abnormal cycle is destructively self-perpetuating and leads to the accumulation of elastase in the lung and ultimately to tissue damage, destruction of the lung architecture, severe pulmonary dysfunction and, ultimately, death.
  • Supplemental API may reduce the deleterious effects associated with excessive amounts of elastase.
  • API is currently administered intravenously.
  • the Aralast®, Zemaira® and Prolastin® brands of human Alpha-1-Proteinase Inhibitor are intravenous formulations indicated for augmentation therapy in patients having congenital deficiency of API with clinically evident emphysema.
  • An API formulation for efficient administration in inhalation is highly desired, and not yet commercially available due to problems in achieving suitable quantity, dispersion and activity of the protein.
  • International Application WO2005048985 discloses compositions comprising API, which further comprise a stabilizing carbohydrate, a surfactant and an antioxidant to stabilize the API for use as a therapeutic, wherein the composition is preferably formulated to be administered by inhalation.
  • nebulizer providing an increased amount of aerosol during inhalation while minimizing both aerosol losses during exhalation and the residual drug in the nebulizer reservoir.
  • the nebulizer includes an aerosol generator that atomizes the liquid through a vibrating diaphragm into particle sizes that are efficiently delivered to the lungs. This nebulizer is currently commercialized under the trade name eFlow®.
  • eFlow® incorporates a “gentle” aerosolization mechanism that minimizes exposure of the drug to shear stresses by reducing the shear stresses and the residence time in the shear fields and does not heat the liquid formulation.
  • International Applications WO 03/026832; WO 2004/014569; WO 2004/052436 and U.S. Pat. No. 5,518,179 disclose further aspects of the eFlow® technology.
  • nebulizer disclosed in WO 01/34232 is exemplified with a salbutamol/sulfate solution and a budesonide suspension.
  • Alpha anti-trypsin is listed as a potential active agent for use with that nebulizer.
  • U.S. Pat. No. 6,655,379 discloses a method and device for the pulmonary delivery of an active agent formulation where inspiratory flow rate of the active agent formulation is less than 17 liters/min.
  • the active agent formulation may be provided in dry powder, in nebulized form, or in the form of aerosolized particles in admixture with a propellant. That invention is exemplified in conjugation with inhalable insulin powder.
  • the present invention relates to a system and methods of treating pulmonary diseases in a subject in need thereof.
  • the system and methods provide administration to the subject of a composition comprising API in the form of an aerosol.
  • the aerosol is produced by nebulizing the API composition in an electronic nebulizer.
  • the nebulizer is eFlow® electronic nebulizer, as disclosed in International Application WO 01/34232
  • the API composition is a ready-to-use solution comprising highly pure, active API, as disclosed in International Application WO 2005/027821.
  • the present invention discloses an inhalation system providing high amounts of active API within the desired location of the lung tissues, thus enabling an efficient treatment of pulmonary diseases.
  • the invention is based in part on the unexpected discovery that pulmonary delivery of a composition comprising less than 10% (weight/volume) API nebulized in the eFlow® nebulizer is efficient and effective.
  • the API composition is preferably a ready-to-use sterilized liquid composition comprising highly pure, active API.
  • the present invention now shows that the activity of API after nebulization remains at above 90% of the activity before nebulization, and, due to the high purity of the composition there is no evidence of dimers, oligomers or aggregates formed in the API aerosol as a result of the nebulization process.
  • the majority of aerosol droplets is in a size range of less than 5 ⁇ m and more specifically between 1 and 4 ⁇ m enabling maximal uptake in the peripheral lung regions.
  • using the system of the present invention reduces inhalation time due to a high liquid output rate and efficient delivery of the active API to the lung.
  • the ready-to-use stable liquid formulation, comprising highly pure, active API is convenient and provides improved dosing accuracy compared to lyophilized products.
  • the present invention provides a system for the treatment of pulmonary diseases comprising:
  • a pharmaceutical composition comprising a purified, stable, active alpha-1 proteinase inhibitor (API) in a form of a ready to use sterile solution; and
  • API active alpha-1 proteinase inhibitor
  • the pharmaceutical composition is nebulized by the inhalation nebulizer to form an aerosol composition.
  • the liquid composition is packed in a pre-sterilised unit dose.
  • the API in the pharmaceutical composition is purified from a partially purified mixture of proteins by a process comprising chromatography on a plurality of ion exchange resins, as disclosed in International Application WO 2005/027821 to one of the Applicants of the present invention.
  • the API in the pharmaceutical composition is preferably purified from a partially purified mixture of proteins by a process comprising chromatography on at least two anion exchange resins and at least one cation exchange resin.
  • the concentration of API in the pharmaceutical composition is less than 10% (weight per volume; w/v). In certain embodiments the concentration of API is between about 1% to about 5%, preferably about 2%. In another embodiment the pH of the pharmaceutical composition is in the range of 6.5-7.5. In yet further embodiment, the pharmaceutical composition is devoid of a protein stabilizer.
  • the purified AAT is at least 90% pure. According to preferred embodiments the purified AAT is at least 95%, more preferably at least 99% pure. According to some embodiments, at least 90% of the API is in its active form.
  • the mass median diameter of the aerosol droplet size distribution is less than about 5 ⁇ m; preferably the mass median diameter of the aerosol droplets is between about 1 ⁇ m and about 4 ⁇ m, more preferably between about 2.0 ⁇ m and about 3.5 ⁇ m and most preferably between about 2.5 ⁇ m to about 3.3 ⁇ m.
  • GSD geometric standard deviations
  • At least a fraction of 50%, preferably 60%, more preferably 70% and more of the loaded nominal dose of API is dissolved in droplets having a diameter from about 1.1 ⁇ m to about 4.7 ⁇ m.
  • the present invention provides a method for treating pulmonary diseases or disorder comprising:
  • a pharmaceutical composition comprising a purified, stable, active alpha-1 proteinase inhibitor in a form of a ready to use sterile solution; and b) an inhalation nebulizer comprising
  • At least 50% of the loaded nominal dose of API can be delivered to the subject, preferably 60% and more preferably 70% or more of the API is delivered to the subject.
  • the API is absorbed by lung tissues of the subject.
  • the pulmonary disease or disorder is selected from the group consisting of emphysema, including inherited emphysema; chronic obstructive pulmonary disease (COPD); bronchiectasis (chronic dilatation of the bronchial tubes); fibrotic lung diseases or disorders including cystic fibrosis, interstitial pulmonary fibrosis and sarcoidosis; tuberculosis; and pulmonary diseases secondary to HIV.
  • COPD chronic obstructive pulmonary disease
  • bronchiectasis chronic dilatation of the bronchial tubes
  • fibrotic lung diseases or disorders including cystic fibrosis, interstitial pulmonary fibrosis and sarcoidosis; tuberculosis; and pulmonary diseases secondary to HIV.
  • API is required to balance the excess concentration of neutrophil elastase present during episodes of inflammation and stress that occur in pulmonary diseases at the phase of exacerbation.
  • the high amounts of active API that can be delivered to the lung tissue by the system and method of the present invention makes it highly suitable to treat pulmonary diseases at the phase of exacerbation.
  • the system and/or method is used for treating a pulmonary disease at a phase of acute exacerbation of the disease.
  • the disease is selected from the group consisting of emphysema, chronic obstructive pulmonary disorder (COPD), bronchiectasis, other parenchymatic or fibrotic lung diseases including cystic fibrosis, interstitial pulmonary fibrosis and sarcoidosis, tuberculosis and pulmonary diseases secondary to HIV.
  • COPD chronic obstructive pulmonary disorder
  • bronchiectasis other parenchymatic or fibrotic lung diseases including cystic fibrosis, interstitial pulmonary fibrosis and sarcoidosis, tuberculosis and pulmonary diseases secondary to HIV.
  • a subject is a human subject.
  • the human subject may be an adult, a child or an infant.
  • FIG. 1 shows the drug delivery profile after breath simulation with API.
  • the present invention discloses a system and methods of treating a pulmonary disease in a subject in need thereof, comprising the administration of a ready to use liquid pharmaceutical composition comprising a purified, stable, active alpha-1 proteinase inhibitor (API) in the form of an aerosol produced by nebulizing the API composition, particularly nebulizing the API composition in an eFlow® nebulizer.
  • API proteinase inhibitor
  • Inhalation delivery is directed to the target site, such that there is negligible systemic absorption and side effects are minimized; it requires lower therapeutic doses, and thus there is a greater product availability; it provides quick relief of symptoms and expected good tolerance; it is more convenient form for patients thus better compliance is expected; and it reduces treatment costs as a result of efficient utilization of an expensive drug using stable, purified API with a highly efficient nebulizer such as the eFlow®.
  • the aerosol droplets retain high activity of alpha-1 proteinase inhibitor: an activity of greater than 90% is desired;
  • the nebulization does not promote API dimerization, oligomerization or aggregation
  • Aerosol median droplet size of less than 5 ⁇ m
  • the present invention provides a system comprising pure API delivered via the eFlow® nebulizer exhibiting, inter alia, the aforementioned advantageous properties. Additionally, the present invention further provides a liquid composition comprising API at a concentration of less than 10% w/v, preferably a ready-to use liquid composition.
  • the high activity and purity of the API composition in combination with the gentle vibrating membrane aerosolization mechanism ensures delivery of highly active API.
  • the ready-to-use stable liquid formulation is convenient to use and obviates the problem of dose preparation and dosing accuracy.
  • API Alpha-1 Proteinase Inhibitor
  • AAT alpha-1 antitrypsin
  • SEpin Serine Proteinase Inhibitor family of proteolytic inhibitors. This glycoprotein consists of a single polypeptide chain containing one cysteine residue and 12-13% carbohydrates of the total molecular weight. API has three N-glycosylation sites at asparagine residues 46, 83 and 247, which are occupied by mixtures of complex bi- and triantennary glycans.
  • API serves as a pseudo-substrate for elastase; elastase attacks the reactive center loop of the API molecule by cleaving the bond between methionine 358 -serine 359 residues to form an API-elastase complex.
  • glycoprotein refers to a protein or peptide covalently linked to a carbohydrate.
  • the carbohydrate may be monomeric or composed of oligosaccharides.
  • eFlow® nebulizer refers to the nebulizer disclosed in international application WO 01/34232.
  • inhalation nebulizer refers to a nebulizer comprising the basic elements of the eFlow® nebulizer and any equivalent nebulizer.
  • pulmonary delivery and “respiratory delivery” refer to delivery of API to a patient by inhalation through the mouth and into the lungs.
  • treat and “treating” includes preventing, alleviating, ameliorating, halting, restraining, slowing or reversing the progression, or reducing the severity of pathological conditions described above. As such, these methods include both medical therapeutic (acute) and/or prophylactic (prevention) administration as appropriate.
  • CF cystic fibrosis
  • CFTR cystic fibrosis transmembrane conductance regulator
  • epiphysema refers to a pathological condition of the lungs in which there is a decrease in respiratory function and often breathlessness due to an abnormal increase in the size of the air spaces, caused by irreversible expansion of the alveoli and/or by the destruction of alveolar walls by neutrophil elastase.
  • COPD chronic obstructive pulmonary disease
  • chronic obstructive pulmonary disease refers to lung disease characterized by obstruction to airflow that interferes with normal breathing.
  • COPD is the fourth leading cause of death in America, claiming the lives of 120,000 Americans in 2002.
  • Smoking is the primary risk factor for COPD with approximately 80% to 90% of COPD deaths are caused by smoking.
  • bronchiectasis refers to a congenital or acquired disorder associated with abnormal bronchial dilatation with bronchial wall destruction and transmural inflammation. The most important functional finding of altered airway anatomy is severely impaired clearance of secretions from the bronchial tree.
  • TB refers to the disease caused by the M. tuberculosis bacterium. TB is an airborne, chronic bacterial infection.
  • exacerbation refers to an increase in the severity of symptoms during a course of a disease which is mostly associated with a worsening of quality of life. Exacerbations are quite frequent in patients with chronic lung diseases and more specifically in API deficient patients. By definition, exacerbations are simply a worsening and/or increase in symptoms.
  • Emphysema is a pathological condition of the lungs marked by an abnormal increase in the size of the air spaces, resulting in strenuous breathing and an increased susceptibility to infection. It can be caused by irreversible expansion of the alveoli or by the destruction of alveolar walls.
  • Congenital emphysema also known as Alpha-1 Antitrypsin (AAT) deficiency or inherited emphysema, is a genetic disorder that increases the risk of developing a variety of diseases including pulmonary emphysema and cirrhosis of the liver. It is caused by mutation in the gene coding for API, the body major serine proteinase inhibitor or serpin.
  • This gene is located in the long arm of chromosome 14 of the human genome.
  • the genetic deficiency can result in life-threatening liver disease in children and adults or in lung disease in adults.
  • an inherited mutation of the API gene causes the build up of abnormal API within the hepatocytes of the liver.
  • the liver is the major source of circulating API and this transport problem leads to low levels of API in the blood and tissue.
  • Various mutations of the API gene exist, most of them associated with deficiency in circulating API. Genotypes that lead to the production of a protein that is dysfunctional as an elastase inhibitor and cause increased risk of emphysema, but are released at a normal level to the circulation have been also identified.
  • the method of the present invention is used for treating lung diseases and disorders associated with cystic fibrosis.
  • the membrane defect caused by the CFTR mutation leads to chronic lung inflammation and infection.
  • Chronic lower respiratory infection provokes a persistent inflammatory response in the airway, resulting in chronic obstructive disease.
  • CF patients become prone to episodes of exacerbation, characterized by worsening symptoms of respiratory infection, particularly by Pseudomonas aeruginosa , accompanied by acute decline in lung function.
  • Loss of pulmonary function is a primary cause of death in patients suffering from cystic fibrosis.
  • Patients with a Forced Expiratory Volume in one second (FEV1) below 30% of their predicted value have a 2-year mortality of greater than 50%.
  • the current mortality rate is 1.2 deaths per 100 patients per year; the median survival is 32 years.
  • 94% were due to cardiorespiratory failure.
  • Respiratory failure is characterized by increasing dyspnea, hypoxemia and elevation of arterial PCO 2 .
  • CF patients are restricted in their day-to-day activities due to reduced lung function and constant pulmonary infections as a result of their condition.
  • CF chronic infection associated with CF
  • phagocytic neutrophils secrete elastase, which has the potential to destroy the elastic tissue of the lung.
  • neutrophils of patients with CF have been shown to be in a state of increased responsiveness and tend to degranulate more readily, releasing tissue-destroying elastase.
  • patients with CF appear to have a state of unregulated inflammatory response, which overwhelms the normal protease (elastase)/antiprotease (API) balance, leading to the accumulation of elastase in the lung and ultimately to tissue damage.
  • protease elastase
  • API antiprotease
  • API is administered to CF patients by the inhalation route. It has been previously demonstrated (McElvaney et al, 1991) that aerosolized alpha-anti-trypsin given to cystic fibrosis patients suppressed neutrophil elastase in the respiratory epithelial lining fluid (ELF), restored the anti-neutrophil elastase capacity in the ELF and reversed the inhibitory effect of the ELF on the ability of neutrophils to effectively combat Pseudomonas infections.
  • aerosol compositions comprising active API can be readily produced using the system of the present invention.
  • Bronchiectasis is an abnormal dilation of the proximal medium-sized bronchi (>2 mm in diameter) caused by destruction of the muscular and elastic components of the bronchial walls. It can be congenital or acquired.
  • Congenital bronchiectasis usually affects infants and children and results from developmental arrest of the bronchial tree.
  • the more commonly acquired forms occur in adults and older children and require an infectious insult, impairment of drainage, airway obstruction, and/or a defect in host defence.
  • the latter may be mediated in part by inflammatory cytokines, nitric oxide, and neutrophilic proteases.
  • peribronchial alveolar tissue may be damaged, resulting in diffuse peribronchial fibrosis.
  • Tuberculosis has recently re-emerged as a public health problem. Most persons that are infected with Mycobacterium tuberculosis harbour the bacterium without symptoms but many develop active TB disease. Each year, 8 million people worldwide develop active TB and 3 million die.
  • MDR-TB Multidrug-resistant TB
  • Treatment for MDR-TB often requires the use of special TB drugs, all of which can produce serious side effects.
  • MDR-TB patients may have to take several antibiotics, at least three to which the bacteria still respond, every day for up to two years.
  • MDR-TB will die, which is the same as for patients with standard TB who do not receive treatment. Palliative therapy for these patients is needed.
  • a purified stable composition of API is provided.
  • a liquid composition of purified, stable of API is provided.
  • International application WO 2005/027821 to one of the applicants of the present invention, provides pharmaceutical compositions comprising a purified, stable, active API in a form of a ready to use sterile solution.
  • WO 2005/027821 also provides process, which combines removal of contaminating substances (i.e., lipids, lipoproteins and other proteins) and separation of active from inactive API by sequential chromatography steps. The process disclosed in that invention is suitable for a large-scale production of API.
  • the mixture of proteins from which the API is purified is preferably Cohn Fraction IV-1 paste, but can include other Cohn Fractions, separately or in combination; human blood plasma; plasma fractions; or any protein preparation containing API.
  • the process is applicable to purification of recombinant human API from the milk of transgenic animals.
  • the mixture of proteins comprising API is dispersed in an aqueous medium, preferably water, at a ratio of between about 20 to about 35 liter per about 1 kg of source material, preferably Cohn Fraction IV-1 paste.
  • the pH of the dispersion is adjusted to a pH range of from about 8.0 to about 9.5.
  • the pH adjustment stabilizes the API and promotes the dissolution of the API in the dispersion, thereby increasing the production yield.
  • Dispersion may take place at an elevated temperature of between 30° C. and 40° C., for further increase in API solubility.
  • a particular advantage of that process is the elimination of contaminants or by-products that otherwise compromise the efficiency of API purification processes.
  • Cohn Fraction IV-1 paste preparations contain a significant amount of the lipoprotein Apo A-1, which has the effect of compromising column flow and capacity during purification.
  • Other non-desired proteins such as albumin and transferrin are also present in the paste preparation.
  • Removing a portion of such contaminants according to the invention disclosed in WO 2005/027821 is performed by two steps: (a) removing contaminating lipids and lipoproteins by lipid removal agent and (b) precipitating a portion of contaminating protein from the API-containing aqueous dispersion.
  • the removal of contaminating proteins, without loss of API enables a significant reduction in equipment scale, e.g., column size.
  • the precipitate that forms can be separated by conventional means such as centrifugation or filtration, and is then discarded.
  • the supernatant is ready for further purification, for example an anion exchange resin.
  • the API is then eluted from the column.
  • the solution is treated to reduce its water content and change the ionic composition by conventional means such as by diafiltration, ultrafiltration, lyophilization, etc., or combinations thereof.
  • the API-containing effluent obtained after the first anion exchange chromatography is concentrated by ultrafiltration.
  • the retentate is then diafiltered against pure water to reach conductivity within the range of from about 3.5 to about 4.5 mS/cm.
  • the solution is loaded on a cation exchange resin with the same type of buffer used for the anion-exchange step, having appropriate pH and conductivity such to allow the API to pass and be washed off with the buffer flow through, while contaminating substances are retained on the cation exchange resin.
  • the API-containing solution obtained after the cation exchange chromatography can be treated to reduce its water content.
  • the solution is concentrated by ultrafiltration.
  • the buffer is any suitable acid/salt combination that provides acceptable buffer capacity in ranges of pH required throughout the API purification process.
  • the buffer used throughout the process is not citrate-based buffer, more preferably the buffer anion is acetate.
  • the process of that invention further comprises viral removal and/or viral inactivation steps.
  • Methods for viral removal and inactivation are known in the art.
  • the viral removal step comprises filtration.
  • the virus removal step is performed after the cation exchange chromatography. Typically, the cation exchange flow-through solution containing API is concentrated, and then nanofiltered.
  • the method of viral inactivation employed comprises a solvent/detergent (S/D) treatment.
  • the viral inactivation step is preferably performed prior to loading the solution on the second anion exchange resin.
  • the detergent used is polysorbate and the solvent is Tri-n-Butyl-Phosphate (TnBP).
  • the polysorbate is polysorbate 80.
  • Polysorbate 80 may be added at from about 0.8% to about 1.3% volume per weight (v/w) of the resulting mixture and TnBP may be added from about 0.2% to about 0.4% weight per weight of the resulting mixture.
  • the solution containing active, purified API obtained after the second anion exchange chromatography can be further processed to obtain a pharmaceutical composition for therapeutic, diagnostic, or other uses.
  • the process further comprises the steps of changing the ionic composition of the solution containing purified, active API to contain a physiologically compatible ion and sterilizing the resulted solution.
  • the purified API obtained by the process of that invention is highly stable.
  • the pharmaceutical composition disclosed in WO 2005/0278 and used with the system and methods of the present invention comprises at least 90% pure, preferably 95% pure, more preferably 99% pure API.
  • at least 90% of the API is in its active form.
  • composition is intended to be used herein in its broader sense to include preparations containing a protein composition in accordance with this invention used for therapeutic purposes.
  • the pharmaceutical composition intended for therapeutic use should contain a therapeutic amount of API, i.e., that amount necessary for preventative or curative health measures.
  • terapéuticaally effective amount refers to an amount of a protein or protein formulation or composition which is effective to treat a condition in a living organism to whom it is administered over some period of time.
  • compositions of the present invention may be manufactured by processes well known in the art, e.g. by means of conventional mixing, dissolving, granulating, grinding, pulverizing, dragee-making, levigating, emulsifying, encapsulating, entrapping or lyophilizing processes.
  • compositions for use in accordance with the present invention thus may be formulated in conventional manner using one or more acceptable diluents or carriers comprising excipients and auxiliaries, which facilitate processing of the active compounds into preparations, which can be used pharmaceutically. Proper formulation is dependent on the route of administration chosen. According to certain currently preferred embodiments, the pharmaceutical compositions of the present invention are formulated in a form suitable for inhalation.
  • API-containing pharmaceutical compositions disclosed in WO 2005/027821 to one of the Applicants of the present invention is advantageous over hitherto known API-containing preparations, as the API is highly stable also when the composition is kept in a liquid form. Therefore, it is not necessary to lyophilize the API-preparation for stable storage in a form of a powder. Subsequently, there is no need to reinstate the powder to a liquid before use for parenteral administration or for inhalation. According to certain preferred embodiment, ready-to use liquid pharmaceutical composition is used with the system of the present invention.
  • the liquid pharmaceutical composition can be packed in pre-sterilised unit dose vials containing 0.25-10 ml made of glass or polymeric materials or filled into polyethylen or any other suitable polymer vials manufactured for instance by a blow fill seal process, commonly used for ready to use inhalation solutions, having typical volume contents from 0.25 ml to 5 ml.
  • API is used for the treatment of pulmonary diseases.
  • most of the API never reaches the lung. It has been estimated that only 2% of the intravenously administered dose reaches the lung (Hubbard & Crystal, 1990).
  • API by the inhalation route may be more beneficial as it reaches directly the lower respiratory tract.
  • the present invention now discloses inhalation route which requires lower therapeutic doses of API and thus the scarce supply of human plasma-derived API would be available for the treatment of more patients.
  • This route of administration may be also more effective in neutralizing neutrophil elastase, and thus the system and methods of the present invention are highly suitable for treating pulmonary diseases at periods of exacerbation.
  • administration by inhalation is simpler and less stressful for the patient than the intravenous route and would reduce the burden on the local health care system (by requiring less clinical input).
  • Formulations of pharmaceutical compositions for administration by the route of inhalation are known in the art.
  • the active ingredients are delivered in the form of an aerosol spray from a pressurized metered dose inhaler with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichloro-tetrafluoroethane or carbon dioxide, in powder form administered using a dry powder inhaler or, in aqueous liquid aerosol form using a nebulizer.
  • a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichloro-tetrafluoroethane or carbon dioxide
  • Nebulizers for liquid aerosol delivery may be categorized as jet nebulizers operated by a pressurized flow of air using a portable compressor or central air supply in a hospital, ultrasonic nebulizers incorporating a piezo-crystal to provide the energy for generating the aerosol out of an ultrasonic fountain, and novel electronic nebulizers based on the principle of a perforated vibrating membrane, such as the eFlow® nebulizer. All nebulization principles involve the aqueous solution being exposed to shear stresses, which may negatively affect the delicate nature of proteins such as API. However, the present invention now discloses that the vibrating membrane principle incorporated in the eFlow® nebulizer can retain the integrity of the API protein structure and, thus, is best suited for pulmonary administration of the API.
  • the overall efficiency of the system of the present invention is superior over hitherto known inhalation systems, for example, the “Akita” inhalation management system associated with a customised PARI LC STAR nebulizer.
  • the drug residue is only about 15% or less, whereas in a jet nebulizer like the LC STAR used in combination with Akita, the residue is at least 40% or more of the loaded dose resulting in a lower delivered dose in droplets of 5 ⁇ m or less compared to the system of the present invention.
  • This novel feature allows for a more efficient and economic drug administration when using eFlow® in combination with the API.
  • the operating conditions for delivery of a suitable inhalation dose vary according to the type of mechanical device employed.
  • the frequency of administration and operating period will be dictated chiefly by the amount of the active composition (API according to the present invention) per unit volume in the aerosol.
  • API active composition
  • Some devices such as metered dose inhalers may produce higher aerosol concentrations than others and thus will be operated for shorter periods to give the desired result.
  • the present invention now discloses that providing composition comprising less than about 10%, preferably less than about 5% of highly purified, stable API, nebulized in the eFlow® nebulizer is highly efficient and effective in treating pulmonary disease.
  • the system and/or method of the present invention is used for treating pulmonary emphysema. It is known that patients with API deficiency have a low level of API and a high burden of neutrophils in their lower respiratory tracts. This observation supports the hypothesis that a deficiency of API predisposes a patient to emphysema by altering the balance between neutrophil elastase and anti-neutrophil elastase in the lower respiratory tract. Whereas normal persons have an adequate anti-neutrophil elastase screen to protect the lower respiratory tract, those with API deficiency do not, permitting the neutrophil elastase to destroy lung tissue. Thus, providing patient with endogenous API-deficiency with exogenic API at the correct dose and location can overcome the deleterious effects of such deficiency.
  • the study described hereinbelow examined the nebulization characteristics of an Alpha-1 Protease Inhibitor (API) solution when nebulized with eFlow® electronic nebulizer (PARI GmbH, Germany, a company specialized in nasal and pulmonary drug delivery).
  • API Alpha-1 Protease Inhibitor
  • the set of experiments was carried out using a liquid formulation of Alpha-1 Proteinase Inhibitor (API), also suitable for injection (Kamada Ltd., Israel).
  • the eFlow® electronic inhaler used is an electronic nebulizer system based on a vibrating membrane principle, as disclosed in International Patent Application WO 01/34232.
  • eFlow® is designed to improve the delivery efficiency and utilization of an aerosolized drug. This is achieved by a vibrating membrane technology generating an aerosol with a very narrow droplet size distribution, expressed by a smaller GSD compared to jet nebulizers (1.7 vs. 2.1) (Balcke, et al., 2004).
  • the unique configuration of the eFlow® nebulizer results in a reduction in the percentage of coarse droplet and elevation of the percentage of very fine droplets, and thus facilitates a better targeting of the active pharmaceutical ingredient, particularly API, to the lung. This is particularly important for expensive drugs of limited availability, such as Alpha-1 Protease Inhibitor.
  • nebulizers The delivery performance of nebulizers depends on the airflow pattern of a tidally breathing patient; therefore, a breath simulator was used to determine the dose of the drug delivered and the time required for nebulizing the entire amount of a drug composition, particularly a liquid drug composition.
  • a standardized breathing manoeuvre was examined to determine the delivered dose, the drug residue in the device and the aerosol loss during exhalation (collected on “exhalation” filters to ensure recovery of the drug amount).
  • An additional assay was conducted using a breathing pattern with reduced inhalation and a prolonged exhalation time, which mimics the breathing pattern of an emphysema patient.
  • API solution 2% (Kamada, Lot A and Lot B)
  • Extraction buffer The extraction buffer was prepared by dissolving 0.57 g NaH 2 PO 4 —H 2 O and 1.46 g NaCl in water “Milli-Q” grade and adjusting the pH to 6.9 to 7.7. The solution volume was then completed with “Milli-Q” water to a final volume of 500 ml.
  • API activity was determined by measuring the extent of inhibition of proteolytic activity of porcine pancreatic elastase on the substrate succinyl-alanine-alanine-alanine-p-nitroanilide. The proteolytic activity was determined spectrophotometrically by the rate of appearance of the reaction product p-nitroaniline.
  • the degree of inhibition of proteolytic activity induced by API is obtained by calculating the ratio of the reaction rate with non-inhibited porcine pancreatic elastase (no API in the reaction medium) to the reaction rate in the presence of API.
  • the activity is expressed in mg API/ml. Presence of dimers/oligomers was examined by Size Exclusion HPLC, performed with Zorbax GF-250 GPC Column.
  • the aerodynamic droplet size distribution was investigated by cascade impactor methods. Two different methods were used.
  • the Andersen Cascade Impactor (ACI) is a traditional impactor type, which has been used in the past to characterize a wide range of different aerosols.
  • the Next Generation Pharmaceutical Impactor (NGI) is a new impactor type, which has been specially designed for the characterization of pharmaceutical aerosols (Marple, et al., 2003a, 2003b, 2004) and has been recently introduced into the European Pharmacopoeia.
  • Non-aerosolized API Two control samples (non-aerosolized API) were prepared by filling around 0.5 g of API solution into polypropylene (PP) tubes and adjusting the weight with extraction buffer to around 13 g. All samples were stored at 2° C. to 8° C. until analysis.
  • Samples were analyzed utilizing the API activity assay described above and evaluated with respect to droplet size distribution pattern, Mass Median Aerodynamic Diameter, Geometric Standard Deviation and Respirable Fraction (% ⁇ 5 ⁇ m) using the software package CITDAS.
  • a breath simulation apparatus was employed to characterize the drug delivery performance of the API/eFlow® system under simulated breathing conditions.
  • the nebulizer was loaded with a dose of 80 mg/4 ml and connected to the breath simulator, which generates the desired human breathing pattern.
  • the tests were performed according to the following protocol: The nebulizer was connected to a sinus pump (PARI breath simulator) mimicking a standard breathing pattern of an adult (500 ml tidal volume, 15 breaths/minute, inhalation:exhalation ratio 1:1, pattern S, Table 1). Alternatively, two modified patterns, which are used as models for impaired breathing patterns of emphysema patients, were employed (E1 and E2, Table 1).
  • Filters collecting the inhaled and exhaled aerosol (“inhalation” and “exhalation” filters, respectively) were installed between the nebulizer and the pump via a Y-piece.
  • the nebulizer was filled with 4 ml of the API formulation for inhalation and run until all the solution was nebulized (nebulization time). Nebulization was interrupted at 3-minute intervals to change saturated filters.
  • the aerosol (containing the API as the drug substance) was collected on the filters.
  • API Delivered Dose is the amount of aerosol that would be inhaled by the patient ex mouthpiece, as well as the amount of aerosolized API lost during exhalation.
  • Inhalation filters were changed after 3 and 6 minutes and after the end of nebulization. Proteins were extracted from the filters by placing the filters in a polypropylene (PP) test tube and adding 30 g of extraction buffer. The tubes were then shake at 250 rpm for 30 min., and the solution was separated from filters by decanting into new PP tubes. The amount of API remained as residue inside the nebulizer was measured by rinsing the nebulizer with 15 g extraction buffer.
  • PP polypropylene
  • the value of the in-vitro respirable dose is based on the delivered dose taking into account the fraction of droplets which are in the respirable size range, i.e. in the range of ⁇ 5 ⁇ m.
  • the in-vitro respirable dose was calculated by multiplying the Delivered Dose and the Respirable Fraction determined during aerosol droplet size characterization.
  • Table 2 summarizes the API characterizations before (control) ant after nebulization (test).
  • API distribution data determined by breath simulation mean ⁇ SD Delivered Dose (mg) 65.3 3.2 Drug residue (mg) 14.4 3.6 Aerosol loss (mg) 13.9 2.5 Nebulization time (min) 9.0 1.0 Delivered Dose (%) 70.0 3.2 Drug residue (%) 15.4 3.9 Aerosol loss (%) 14.9 2.6
  • the additional experiments show delivered dose values in the range from 55% to 57% of loaded dose. There appears to be no difference in delivered dose values between the two patterns. Hence, mean values were calculated from all four runs.
  • the series of breath simulations show that around 70% of the loaded dose can be delivered ex-mouthpiece of the nebulizer with a breathing pattern reflecting a normally breathing patient and around 56% can still be delivered for a severely impaired breathing pattern.
  • Aerodynamic droplet size distribution was analyzed using an Andersen Cascade Impactor (ACI) fitted with an USP-throat (Copley Scientific Instruments, Nottingham, UK).
  • ACI Andersen Cascade Impactor
  • USP-throat Copley Scientific Instruments, Nottingham, UK
  • the ACI was equilibrated at 18° C. using a water bath. Environmental conditions were controlled at 23° C. and 50% relative humidity.
  • the nebulizer was filled with 4 ml of formulation and connected to the USP-throat. The airflow rate through the nebulizer and impactor was set at 28.3 L/min. The nebulizer was operated until nebulization was complete. Then the ACI was disassembled, plates and USP-throat were rinsed with 10 ml of phosphate buffer. The drug content was analyzed for each impactor stage and the USP throat separately.
  • the Mass Median Aerodynamic Diameter (MMAD) was calculated according to USP methods, using the CITDAS software
  • NTI Next Generation Impactor
  • Aerodynamic droplet size distribution was also analyzed using a Next Generation Pharmaceutical Impactor (NGI) fitted with a USP-throat (Copley Scientific Instruments, Nottingham, UK).
  • NGI Next Generation Pharmaceutical Impactor
  • eFlow® was filled with 4 ml of API formulation and connected to the USP-throat.
  • the nebulizer was operated until nebulization was completed, and then the NGI was disassembled.
  • the API content was analyzed for each impactor stage and the USP throat separately.
  • the Mass Median Aerodynamic Diameter (MMAD) was calculated according to USP methods, using the software package CITDAS (Copley Scientific Instruments, Nottingham, UK).
  • the NGI was operated at a flow of 15 ⁇ 0.5 l/min at 22° C. ⁇ 2° C. and at 50% ⁇ 5% relative humidity (r.h.).
  • the NGI cups were weighted before and after loading.
  • the API on the single stages was extracted with 10 ml extraction buffer for 30 min.
  • the NGI inlet was rinsed with 20 g and the nebulizer with 15 g extraction buffer (weight recorded).
  • the geometric droplet size distribution was characterized by a diffractometer Mastersizer X (Malvern Instruments,dorfberg, Germany). Environmental conditions were controlled at 23° C. and 50% relative humidity. The airflow rate through the nebulizer and diffractometer was set at 201/min. The Mass Median Diameter (MMD) was calculated according to the Mie-theory choosing the 2QAA presentation model supplied with the Malvern software.
  • the value of the in-vitro respirable dose is derived from the delivered dose determined in the breath simulation experiment and the respirable fraction, i.e. the proportion of the API drug disposed in droplets having a size of ⁇ 5 ⁇ m. Assessment of respirable fraction by three different droplet-sizing methods gave very similar results (between 87.4 and 90.3%) with an average of 88.5 ⁇ 2.15% across all methods. This value is used for the calculation of the respirable dose.
  • Respirable Dose, Drug Delivery Rate and Respirable Drug Delivery Rate API Mean ⁇ SD Respirable Dose (mg ⁇ 5 ⁇ m) 57.8 2.90 Respirable Dose (% of charged amount ⁇ 5 ⁇ m) 61.9 2.79 Drag Delivery Rate (mg/min) 7.4 0.98 Respirable Drug Delivery Rate (mg ⁇ 5 ⁇ m/min) 6.5 0.74
  • the present in-vitro study investigated the nebulization of Alpha-1 Protease Inhibitor (API) solution in combination with the eFlow®, a novel electronic nebulizer.
  • API Alpha-1 Protease Inhibitor
  • API activity in the two tested lots after nebulization by eFlow® was found to be 90.0% to 94.5% of the original activity.
  • the droplet size distribution obtained from the eFlow® was investigated by cascade impaction and laser diffraction.
  • Cascade impaction was conducted using the Next Generation Pharmaceutical Impactor and the Andersen Cascade Impactor.
  • Laser Diffraction was conducted using a Malvern Mastersizer X.
  • the target range of the droplet size was between 1 ⁇ m and 4 ⁇ m. Characterization by three different methods showed a median droplet size, MMD or MMAD, between 3.1 ⁇ m and 3.3 ⁇ m, meeting the desired target, and a respirable fraction of 87% to 90%.
  • the GSD which indicates the scattering of the droplet size distribution, was around 1.5, representing a very narrow size distribution.
  • In-vitro breath simulation tests were conducted to assess treatment time and API delivery, using a standardized breathing pattern representing an adult patient.
  • the volume of API solution filled into the eFlow® was 4.0 ml (equivalent to a nominal dose of 80 mg).
  • the nebulization time was 9.0 ⁇ 0.1 min.
  • An amount of around 65 mg (70%) of active API can be delivered at the mouthpiece of the nebulizer.
  • an in-vitro respirable dose of around 58 mg (62%) can be calculated.
  • Additional tests with a breathing pattern thought to represent a patient suffering from severe emphysema still gave an in-vitro delivered dose of 47 mg (56%).
  • API nebulization of API by eFlow® produces an aerosol suitable to reach the patients lungs.
  • the inhalation of API nebulized with the eFlow® delivers the drug molecules directly to the site of action and reduces the required amount of the scarce and expensive drug. Inhalation of API can help to offer an easy, quick and efficient therapy and can enable more patients suffering from pulmonary disease to receive treatment.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Zoology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Dispersion Chemistry (AREA)
  • Otolaryngology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
US12/278,767 2006-02-09 2007-02-08 Pulmonary delivery of alpha-1 proteinase inhibitor Abandoned US20090304604A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/278,767 US20090304604A1 (en) 2006-02-09 2007-02-08 Pulmonary delivery of alpha-1 proteinase inhibitor

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US77146506P 2006-02-09 2006-02-09
US77365406P 2006-02-16 2006-02-16
PCT/IL2007/000182 WO2007091267A2 (fr) 2006-02-09 2007-02-08 Administration pulmonaire d'un inhibiteur de la protéinase alpha-1
US12/278,767 US20090304604A1 (en) 2006-02-09 2007-02-08 Pulmonary delivery of alpha-1 proteinase inhibitor

Publications (1)

Publication Number Publication Date
US20090304604A1 true US20090304604A1 (en) 2009-12-10

Family

ID=38345545

Family Applications (3)

Application Number Title Priority Date Filing Date
US12/278,767 Abandoned US20090304604A1 (en) 2006-02-09 2007-02-08 Pulmonary delivery of alpha-1 proteinase inhibitor
US12/278,756 Active US7973005B2 (en) 2006-02-09 2007-02-08 Alpha-1 antitrypsin for treating exacerbation episodes of pulmonary diseases
US13/458,957 Abandoned US20120211005A1 (en) 2006-02-09 2012-04-27 Pulmonary delivery of alpha-1 proteinase inhibitor

Family Applications After (2)

Application Number Title Priority Date Filing Date
US12/278,756 Active US7973005B2 (en) 2006-02-09 2007-02-08 Alpha-1 antitrypsin for treating exacerbation episodes of pulmonary diseases
US13/458,957 Abandoned US20120211005A1 (en) 2006-02-09 2012-04-27 Pulmonary delivery of alpha-1 proteinase inhibitor

Country Status (13)

Country Link
US (3) US20090304604A1 (fr)
EP (3) EP2740487B1 (fr)
AU (2) AU2007213343B2 (fr)
BR (2) BRPI0707635A2 (fr)
CA (2) CA2641875C (fr)
DK (1) DK1981572T3 (fr)
ES (2) ES2399449T3 (fr)
HK (1) HK1198919A1 (fr)
MX (2) MX2008010173A (fr)
PL (1) PL1981572T3 (fr)
PT (1) PT1981572E (fr)
RU (2) RU2433841C2 (fr)
WO (2) WO2007091267A2 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150150803A1 (en) * 2011-06-07 2015-06-04 Parion Sciences, Inc. Aerosol delivery systems, compositions and methods
US9987443B2 (en) 2007-10-10 2018-06-05 Parion Sciences, Inc. Inhaled hypertonic saline delivered by a heated nasal cannula
US10335558B2 (en) 2011-06-07 2019-07-02 Parion Sciences, Inc. Methods of treatment
WO2021198115A1 (fr) 2020-04-01 2021-10-07 UNION therapeutics A/S Traitement
WO2021198116A1 (fr) 2020-04-01 2021-10-07 UNION therapeutics A/S Formulation

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2740487B1 (fr) * 2006-02-09 2018-02-28 Kamada Ltd. Alpha-1-Antitrypsine pour le traitement des épisodes d'exacerbation des maladies pulmonaires
ES2679819T3 (es) 2009-11-03 2018-08-31 Grifols Therapeutics Inc. Composición, método y kit para inhibidor de alfa-1 proteinasa
AU2010324839B2 (en) 2009-11-24 2015-02-19 Grifols Therapeutics Inc. Lyophilization methods, compositions, and kits
WO2013096458A1 (fr) * 2011-12-19 2013-06-27 Gtc Biotherapeutics, Inc. Alpha-1-antitrypsine humaine recombinante pour le traitement de troubles inflammatoires
SG2014012066A (en) 2011-12-30 2014-09-26 Grifols Sa Alpha1-proteinase inhibitor for delaying the onset or progression of pulmonary exacerbations
WO2013175007A1 (fr) * 2012-05-25 2013-11-28 Inserm Agents pour le traitement de la mucoviscidose
BR112014030569B1 (pt) 2012-06-08 2021-12-28 Koninklijke Philips N.V Método de monitoramento da função pulmonar de um paciente usando um sistema que tem um aparelho respiratório e uma unidade de processamento, e sistema para uso no monitoramento da função pulmonar de um paciente
US10034921B2 (en) 2013-02-13 2018-07-31 Laboratoire Français Du Fractionnement Et Des Biotechnologies Proteins with modified glycosylation and methods of production thereof
WO2016087582A1 (fr) * 2014-12-03 2016-06-09 Institut National De La Sante Et De La Recherche Medicale (Inserm) Procédés et compositions pharmaceutiques pour la prévention et/ou le traitement d'exacerbations aiguës de la maladie pulmonaire obstructive chronique
PT3463280T (pt) 2016-05-31 2022-10-07 Polyphor Ag Beta-hairpin peptidomimético com atividade inibitória da elastase e respectivas formas de dosagem de aerossóis
EP3348293A1 (fr) 2017-01-17 2018-07-18 Carebay Europe Ltd. Dispositifs d'administration de médicaments
WO2018154568A1 (fr) * 2017-02-21 2018-08-30 Kamada Ltd. Procédés et utilisations de l'alpha 1-antitrypsine pour une intervention précoce dans des maladies pulmonaires
PT3723790T (pt) * 2017-12-12 2024-05-10 Kamada Ltd Métodos de indução de tolerância imunitária e de redução da resposta de anticorpos antifármacos
WO2020157752A1 (fr) * 2019-01-29 2020-08-06 Kamada Ltd Composition d'aérosol pharmaceutique

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4697003A (en) * 1985-11-01 1987-09-29 Miles Laboratories, Inc. Method of preparing alpha-1-proteinase inhibitor
US5093316A (en) * 1986-12-24 1992-03-03 John Lezdey Treatment of inflammation
US5518179A (en) * 1991-12-04 1996-05-21 The Technology Partnership Limited Fluid droplets production apparatus and method
US5618786A (en) * 1987-04-30 1997-04-08 Cooper Laboratories, Inc. Aerosolization of protein therapeutic agent
US5780440A (en) * 1996-06-17 1998-07-14 Protease Sciences Inc. Treatment of pulmonary disease with protease inhibitors
US6462180B1 (en) * 1999-11-24 2002-10-08 Bayer Corporation Method of preparing α-1 proteinase inhibitor
US6655379B2 (en) * 1998-03-16 2003-12-02 Nektar Therapeutics Aerosolized active agent delivery
US20080060640A1 (en) * 2002-12-09 2008-03-13 Pari Gmbh Spezialisten Fur Effektive Inhalation Inhalation Therapy Device
US20090131305A1 (en) * 2006-02-09 2009-05-21 Shabtai Bauer Alpha-1 antitrypsin for treating exacerbation episodes of pulmonary diseases

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19953317C1 (de) 1999-11-05 2001-02-01 Pari Gmbh Inhalationsvernebler
EP1295647A1 (fr) 2001-09-24 2003-03-26 The Technology Partnership Public Limited Company Buses dans des membranes perforées et méthode de fabrication
ATE463304T1 (de) 2002-08-02 2010-04-15 Pari Pharma Gmbh Vorrichtung zur erzeugung von flüssigkeitströpfchen
WO2005027821A2 (fr) 2003-09-22 2005-03-31 Kamada Ltd. Preparation a grande echelle d'un inhibiteur d'alpha-1 proteinase et son utilisation
ATE530165T1 (de) * 2003-11-14 2011-11-15 Baxter Int Alpha1-antitrypsin-zusammensetzungen und behandlungsverfahren unter verwendung dieser zusammensetzungen
US7914771B2 (en) 2004-03-09 2011-03-29 Arriva Pharmaceuticals, Inc. Treatment of chronic obstructive pulmonary disease by low dose inhalation of protease inhibitor

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4697003A (en) * 1985-11-01 1987-09-29 Miles Laboratories, Inc. Method of preparing alpha-1-proteinase inhibitor
US5093316A (en) * 1986-12-24 1992-03-03 John Lezdey Treatment of inflammation
US5618786A (en) * 1987-04-30 1997-04-08 Cooper Laboratories, Inc. Aerosolization of protein therapeutic agent
US5518179A (en) * 1991-12-04 1996-05-21 The Technology Partnership Limited Fluid droplets production apparatus and method
US5780440A (en) * 1996-06-17 1998-07-14 Protease Sciences Inc. Treatment of pulmonary disease with protease inhibitors
US6655379B2 (en) * 1998-03-16 2003-12-02 Nektar Therapeutics Aerosolized active agent delivery
US6462180B1 (en) * 1999-11-24 2002-10-08 Bayer Corporation Method of preparing α-1 proteinase inhibitor
US20080060640A1 (en) * 2002-12-09 2008-03-13 Pari Gmbh Spezialisten Fur Effektive Inhalation Inhalation Therapy Device
US20090131305A1 (en) * 2006-02-09 2009-05-21 Shabtai Bauer Alpha-1 antitrypsin for treating exacerbation episodes of pulmonary diseases

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9987443B2 (en) 2007-10-10 2018-06-05 Parion Sciences, Inc. Inhaled hypertonic saline delivered by a heated nasal cannula
US20150150803A1 (en) * 2011-06-07 2015-06-04 Parion Sciences, Inc. Aerosol delivery systems, compositions and methods
US10335558B2 (en) 2011-06-07 2019-07-02 Parion Sciences, Inc. Methods of treatment
WO2021198115A1 (fr) 2020-04-01 2021-10-07 UNION therapeutics A/S Traitement
WO2021198116A1 (fr) 2020-04-01 2021-10-07 UNION therapeutics A/S Formulation

Also Published As

Publication number Publication date
WO2007091267A2 (fr) 2007-08-16
AU2007213344A1 (en) 2007-08-16
RU2472524C2 (ru) 2013-01-20
BRPI0707634A2 (pt) 2011-05-10
DK1981572T3 (da) 2013-03-04
ES2664624T3 (es) 2018-04-20
EP1981572A2 (fr) 2008-10-22
RU2433841C2 (ru) 2011-11-20
PL1981572T3 (pl) 2013-05-31
AU2007213343A1 (en) 2007-08-16
EP2740487B1 (fr) 2018-02-28
US7973005B2 (en) 2011-07-05
CA2641875A1 (fr) 2007-08-16
WO2007091266A3 (fr) 2007-11-15
EP1981572B1 (fr) 2012-11-21
CA2641875C (fr) 2016-10-04
MX2008010173A (es) 2009-02-12
US20090131305A1 (en) 2009-05-21
WO2007091266A2 (fr) 2007-08-16
CA2641872A1 (fr) 2007-08-16
EP1981531A2 (fr) 2008-10-22
RU2008135580A (ru) 2010-03-20
MX2008010172A (es) 2009-09-07
ES2399449T3 (es) 2013-04-01
RU2008135582A (ru) 2010-03-20
BRPI0707635A2 (pt) 2011-05-10
EP2740487A1 (fr) 2014-06-11
AU2007213343B2 (en) 2012-09-13
HK1198919A1 (en) 2015-06-19
WO2007091267A3 (fr) 2007-11-22
AU2007213344B2 (en) 2012-11-15
US20120211005A1 (en) 2012-08-23
PT1981572E (pt) 2013-02-26

Similar Documents

Publication Publication Date Title
AU2007213344B2 (en) Pulmonary delivery of alpha-I proteinase inhibitor
RU2635482C2 (ru) Ингибитор альфа1-протеиназы для задержки начала или прогрессирования легочных обострений
Vogelmeier et al. The intrapulmonary half-life and safety of aerosolized alpha1-protease inhibitor in normal volunteers.
IL164078A (en) Antithrombin iii for use in treating lung injury
US10960062B2 (en) Methods and uses of alpha 1-antitrypsin for early intervention in pulmonary diseases
US20210008183A1 (en) Methods of inducing immune tolerance and reducing anti-drug antibody response
NZ621596B2 (en) Alpha1-proteinase inhibitor for delaying the onset or progression of pulmonary exacerbations

Legal Events

Date Code Title Description
AS Assignment

Owner name: KAMADA LTD., ISRAEL

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:BAUER, SHABTAI;REEL/FRAME:023222/0753

Effective date: 20081118

Owner name: PARI PHARMA GMBH, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KELLER, MANFRED;KNOCH, MARTIN;REEL/FRAME:023222/0756

Effective date: 20081219

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION