KR970702064A - PHARMACEUTICAL FORMULATION FOR SUBCUTANEOUS, INTRAMUSCULAR OR INTRADERMAL ADMINISTRATION OF FACTOR Ⅷ OR FACTOR Ⅸ For Factor VII or Subcutaneous, Intramuscular or Intradermal Administration of Factor VII - Google Patents

PHARMACEUTICAL FORMULATION FOR SUBCUTANEOUS, INTRAMUSCULAR OR INTRADERMAL ADMINISTRATION OF FACTOR Ⅷ OR FACTOR Ⅸ For Factor VII or Subcutaneous, Intramuscular or Intradermal Administration of Factor VII Download PDF

Info

Publication number
KR970702064A
KR970702064A KR1019960705410A KR19960705410A KR970702064A KR 970702064 A KR970702064 A KR 970702064A KR 1019960705410 A KR1019960705410 A KR 1019960705410A KR 19960705410 A KR19960705410 A KR 19960705410A KR 970702064 A KR970702064 A KR 970702064A
Authority
KR
South Korea
Prior art keywords
factor vii
factor
administration
formulation
formulation according
Prior art date
Application number
KR1019960705410A
Other languages
Korean (ko)
Other versions
KR100373882B1 (en
Inventor
슈피라 야크
비들룬트 라스
외슈터벅 토마스
스외슈트룀 브리타
미카엘손 마리아네
Original Assignee
크리스터 발스트룀
파마시아& 업존 아베
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
Priority claimed from SE9401105A external-priority patent/SE9401105D0/en
Application filed by 크리스터 발스트룀, 파마시아& 업존 아베 filed Critical 크리스터 발스트룀
Publication of KR970702064A publication Critical patent/KR970702064A/en
Application granted granted Critical
Publication of KR100373882B1 publication Critical patent/KR100373882B1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/36Blood coagulation or fibrinolysis factors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/36Blood coagulation or fibrinolysis factors
    • A61K38/37Factors VIII
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43Enzymes; Proenzymes; Derivatives thereof
    • A61K38/46Hydrolases (3)
    • A61K38/48Hydrolases (3) acting on peptide bonds (3.4)
    • A61K38/482Serine endopeptidases (3.4.21)
    • A61K38/4846Factor VII (3.4.21.21); Factor IX (3.4.21.22); Factor Xa (3.4.21.6); Factor XI (3.4.21.27); Factor XII (3.4.21.38)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/42Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/44Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Inorganic Chemistry (AREA)
  • Hematology (AREA)
  • Zoology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)

Abstract

본 발명은 응고 인자 Ⅷ 또는 인자 Ⅸ를 포함하는, 피하, 근육내 또는 피내 투여용의 약제학적 제형물 및 혈우병 A 또는 B를 치료하기 위한 약제의 제조에서 이들을 사용하는 방법에 관한 것이다. 상기 제형물은, 200IU/㎖ 이상의 활성을 가지는 응고 인자 Ⅷ 또는 인자 Ⅸ 및 이들의 생체 이용률을 증가시키는 첨가제를 포함한다. 인자 Ⅷ로의 시험은, 피하, 근육내 또는 피내 투여 후 장시간 동안 혈류 중의 활성 인자 Ⅷ의 치료학적 수준을 제공한다. 인자 Ⅷ는 적합하게 고도로 정제된 재조합 인자 Ⅷ 및 바람직하게는, 피하 투여용의 약제의 제조에서 사용될 수 있는, 인자 Ⅷ의 결실 유도체이다.The present invention relates to methods of using them in the preparation of pharmaceutical formulations for subcutaneous, intramuscular or intradermal administration, including coagulation factor VII or factor VII and medicaments for treating hemophilia A or B. The formulations include coagulation factor VII or factor VII having an activity of at least 200 IU / ml and additives that increase their bioavailability. Testing with factor XV provides therapeutic levels of active factor XV in the bloodstream for a long time after subcutaneous, intramuscular or intradermal administration. Factor VII is a deletion derivative of Factor VII that can be used in the manufacture of suitably highly purified recombinant factor VII and, preferably, a medicament for subcutaneous administration.

Description

인자 Ⅷ 또는 인자 Ⅸ의 피하, 근육내 또는 피내 투여용 약제학적 제형물(PHARMACEUTICAL FORMULATION FOR SUBCUTANEOUS, INTRAMUSC-ULAR OR INTRADERMAL ADMINISTRATION OF FACTOR Ⅷ OR FACTOR Ⅸ)PHARMACEUTICAL FORMULATION FOR SUBCUTANEOUS, INTRAMUSC-ULAR OR INTRADER MAL ADMINISTRATION OF FACTOR Ⅷ OR FACTOR Ⅸ For Factor VII or Subcutaneous, Intramuscular or Intradermal Administration of Factor VII

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (24)

200IU/㎖이상의 활성을 갖는 응고 인자 Ⅷ 또는 인자 Ⅸ 및 이들의 생체 이용률을 증가시키는 첨가제를 포함하는, 피하, 근육내 또는 피내 투여용 약제학적 제형물로서, 투여 후 6시간 이상 동안 혈액내의 인자 Ⅷ 또는 인자 Ⅸ 활성의 치료학적 수준을 정상 혈장 농도의 1.5% 이상으로 제공하는 것을 특징으로 하는 제형물.A pharmaceutical formulation for subcutaneous, intramuscular or intradermal administration, comprising a coagulation factor VII or factor VII having an activity of at least 200 IU / ml and an additive that increases their bioavailability, wherein the factor VII in the blood for at least 6 hours after administration Or a therapeutic level of factor VII activity at at least 1.5% of normal plasma concentration. 제1항에 있어서, 상기 제형물이, 투여 후 혈액내의 인자 Ⅷ 또는 인자 Ⅸ 활성의 치료학적 수준을 혈장 정상 수준의 2.5% 이상으로 제공하는 것을 특징으로 하는 제형물.The formulation of claim 1, wherein the formulation provides a therapeutic level of Factor VIII or Factor VIII activity in the blood after administration at 2.5% or more of normal plasma levels. 제1항 내지 2항에 있어서, 인자 Ⅷ 또는 인자 Ⅸ 활성의 상기 치료학적 수준이 투여 후 12시간 동안 유지되는 것을 특징으로 하는 제형물.The formulation according to claim 1, wherein said therapeutic level of factor VIII or factor VIII activity is maintained for 12 hours after administration. 제1항 내지 3항 중 어는 한 항에 있어서, 첨가제가, 아미노산, 펩티드, 단백질 또는 이들의 조합물로 이루어진 군으로부터 선택되는 것을 특징으로 하는 제형물.The formulation according to any one of claims 1 to 3, wherein the additive is selected from the group consisting of amino acids, peptides, proteins or combinations thereof. 제4항에 있어서, 상기 단백질이 젤라틴 및 콜라겐으로 이루어진 군으로부터 선택되는 것을 특징으로 하는 제형물.The formulation of claim 4, wherein said protein is selected from the group consisting of gelatin and collagen. 제1항 내지 3항 중에 어느 한 항에 있어서, 상기 첨가제가 폴리삭카라이드로 이루어진 군으로부터 선택되는 것을 특징으로 하는 제형물.The formulation according to any one of claims 1 to 3, wherein said additive is selected from the group consisting of polysaccharides. 제6항에 있어서. 상기 폴리삭카라이드가 키토산, 시클로덱스토린, 전분, 덱스트란, 셀룰로오스 및 이들의 유도체 및/또는 이들의 조합물로 이루어진 군으로부터 선택되는 것을 특징으로 하는 제형물.The method of claim 6. Wherein said polysaccharide is selected from the group consisting of chitosan, cyclodextrin, starch, dextran, cellulose and derivatives thereof and / or combinations thereof. 제6항에 있어서, 상기 폴리삭카라이드가 히알루론산으로 이루어진 군으로부터 선택되는 것을 특징으로 하는 제형물.7. The formulation according to claim 6, wherein said polysaccharide is selected from the group consisting of hyaluronic acid. 제1항 내지 3항 중 어는 한 항에 있어서, 상기 첨가제가, 분산상으로서 오일과 오일-인-물(oil-in-water)에멀션, 극성 지질의 분산 및 연속상으로서 오일과 물-인-오일(water-in-oil) 에멀션으로 이루어진 군으로부터 선택되는 것을 특징으로 하는 제형물.The oil and water-in-oil of claim 1, wherein the additive is an oil and oil-in-water emulsion as a dispersed phase, a dispersion of polar lipids and a continuous phase. Formulations selected from the group consisting of (water-in-oil) emulsion. 제9항에 있어서, 상기 오일이 대두유인 것을 특징으로 하는 제형물.The formulation of claim 9, wherein said oil is soybean oil. 제1항 내지 10항 중 어느 한 항에 있어서, 피하 투여용으로 채택되는 것을 특징으로 하는 제형물.The formulation according to any one of claims 1 to 10, which is adopted for subcutaneous administration. 제1항 내지 11항 중 어느 한 항에 있어서, 상기 인자 Ⅷ 또는 인자 Ⅸ의 활성이 500IU/㎖이상, 바람직하게는 1,000IU/㎖ 이상인 것을 특징으로 하는 제형물.The formulation according to any one of claims 1 to 11, wherein the factor VII or factor VII activity is at least 500 IU / ml, preferably at least 1,000 IU / ml. 제1항 내지 12항 중 어느 한 항에 있어서, 0.01㎖ 이상, 바람직하게는 0.1 내지 2㎖의 부피를 가지는 것을 특징으로 하는 제형물.The formulation according to any one of the preceding claims, which has a volume of at least 0.01 ml, preferably 0.1 to 2 ml. 제1항 내지 13항 중 어는 한 항에 있어서, 인자 Ⅷ이 재조합 응고 인자 Ⅷ인 것을 특징으로 하는 제형물.The formulation of claim 1, wherein the factor VII is recombinant coagulation factor VII. 제14항에 있어서, 인자 Ⅷ이 재조합 응고 인자 Ⅷ의 결실 유도체인 것을 특징으로 하는 제형물.The formulation of claim 14, wherein factor VII is a deletion derivative of recombinant coagulation factor VII. 제1항에 있어서, ⅰ) 200IU/㎖이상의 인자 Ⅷ, 바람직하게는, 1,500IU/㎖이상의 재조합 인자 Ⅷ의 결실유도체,ⅱi)0.01㎎/㎖ 이상의 폴리옥시에틸렌 소르비탄 지방산 에스테르, iii)바람직하게는 0.1M 이상의 양의 염화나트륨, ⅳ) 바람직하게는 0.5mM이상의 양의 염화 칼슘 또는 글루콘삼 칼슘과 같은 칼슘염, ⅴ)1mM이상의 양의 L-히스티딘과 같은 아미노산, 및 (ⅶ) 인자 Ⅷ의 생체 이용률을 증가시키는 첨가제를 포함하는 것을 특징으로 하는 제형물.2. A method according to claim 1, comprising: i) a deletion derivative of at least 200 IU / mL of factor VII, preferably at least 1,500 IU / mL of recombinant factor VII, iii) at least 0.01 mg / mL of polyoxyethylene sorbitan fatty acid ester, iii) Is an amount of sodium chloride in an amount of at least 0.1 M, i) preferably a calcium salt such as calcium chloride or gluconium calcium in an amount of at least 0.5 mM, i) an amino acid such as L-histidine in an amount of at least 1 mM, and Formulations comprising additives to increase utilization. 제14항 또는 16항에 있어서, 상기 결실 유도체 인자 Ⅷ가 결실 유도체 재조합 인자 Ⅷ SQ(r-Ⅷ SQ)인 것을 특징으로 하는 제형물.The formulation according to claim 14 or 16, wherein the deletion derivative factor V is a deletion derivative recombinant factor V SQ (r-V SQ). 제1항 내지 17항 중 어느 한 항에 있어서, 투여용으로 안정한 수용액 또는 분산액인 것을 특징으로 하는 제형물.18. The formulation according to any one of claims 1 to 17, which is an aqueous solution or dispersion that is stable for administration. 제18항에 있어서, 투여 전에 1종 이상의 수용액 또는 분산액과 단순 혼합 또는 순서대로 혼합시키는 것을 특징으로 하는 제형물.19. A formulation according to claim 18, characterized in simple mixing or mixing in sequence with one or more aqueous solutions or dispersions prior to administration. 제1항 내지 17항중 어느 한 항에 있어서, 건조된 상태로서, 투여 전에 1종 이상의 수용액 또는 분산액과 임의적으로 또는 연속적으로 재구성되는 것을 특징으로 하는 제형물.18. The formulation according to any one of claims 1 to 17, which is in a dry state, optionally or continuously reconstituted with one or more aqueous solutions or dispersions prior to administration. 제1항 내지 20항 중 어는 한 항에 따른 제형물을 포함하는, 피하, 근육내 또는 피내 투여용의 혈우병 치료 약제.A hemophilia therapeutic agent for subcutaneous, intramuscular or intradermal administration comprising a formulation according to any one of claims 1 to 20. 피하 투여용 약제의 제조에 사용하기 위한 재조합 인자 Ⅷ의 결실 유도체.A deletion derivative of recombinant Factor VIII for use in the manufacture of a medicament for subcutaneous administration. 제21항 내지 22항에 있어서, 안정한 수용액이나 분산액 형태 또는 건조 형태로 사용되는 것을 특징으로 하는 제형물 또는 결실 유도체.23. Formulations or deletion derivatives according to claims 21-22, which are used in the form of stable aqueous solutions or dispersions or in dry form. 제1항 내지 20항 중 어느 한 항에 따른 제형물을 피하, 근육내 또는 피내 투여함으로써 혈우병을 치료하는 방법.A method of treating hemophilia by subcutaneous, intramuscular or intradermal administration of a formulation according to any one of claims 1 to 20. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019960705410A 1994-03-31 1995-03-31 Pharmaceutical formulations for subcutaneous, intramuscular or intradermal administration of factor X KR100373882B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
SE9401105A SE9401105D0 (en) 1993-07-05 1994-03-31 formulation
SE9401105-3 1994-03-31
SE9500036A SE9500036D0 (en) 1995-01-05 1995-01-05 formulation
SE9500036-0 1995-01-05

Publications (2)

Publication Number Publication Date
KR970702064A true KR970702064A (en) 1997-05-13
KR100373882B1 KR100373882B1 (en) 2003-08-02

Family

ID=20396754

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019960705410A KR100373882B1 (en) 1994-03-31 1995-03-31 Pharmaceutical formulations for subcutaneous, intramuscular or intradermal administration of factor X

Country Status (2)

Country Link
KR (1) KR100373882B1 (en)
SE (1) SE9500036D0 (en)

Also Published As

Publication number Publication date
KR100373882B1 (en) 2003-08-02
SE9500036D0 (en) 1995-01-05

Similar Documents

Publication Publication Date Title
FI118171B (en) Pharmaceutical formulation for the subcutaneous, intramuscular or intradermal administration of factor VIII
CA1222948A (en) Enhancement of intranasal absorption of calcitonin by formulation with surfactants
BROWN et al. Acceleration of tensile strength of incisions treated with EGF and TGF-β
RU2424824C2 (en) Complex amphiphilic polimer-pdgf
CA2911046C (en) Pharmaceutical composition comprising a botulinum neurotoxin and uses thereof
EP1731139A1 (en) S/o type pharmaceutical preparation and process for producing the same
EP0767666B1 (en) Methods and compositions useful in prophylaxis and therapy of endotoxin related conditions
Mosquera et al. Incorporation of liposomes containing squid tunic ACE‐inhibitory peptides into fish gelatin
IE60649B1 (en) Mixed crystals of insulin and insulin derivatives, a process for the preparation of these mixed crystals, and pharmaceutical agents containing these mixed crystals
US20110097391A1 (en) Phospholipid Emulsion Containing Dihydroquercetin, and Method of Producing Thereof
ATE92767T1 (en) TOCOPHEROL BASED DRUG SYSTEMS.
KR970702064A (en) PHARMACEUTICAL FORMULATION FOR SUBCUTANEOUS, INTRAMUSCULAR OR INTRADERMAL ADMINISTRATION OF FACTOR Ⅷ OR FACTOR Ⅸ For Factor VII or Subcutaneous, Intramuscular or Intradermal Administration of Factor VII
JP2009096787A (en) Water-dispersible nanoparticle including blood circulation promoter
Brooks et al. Effects of antemortem injected crude papain in chicken muscle
JPH07196510A (en) A sustained release lipid emulsion for analgesic-containing injection solution
IL91928A (en) Pharmaceutical compositions containing prolactin
Maitani et al. The effect of soybean-derived sterol and its glucoside as an enhancer of nasal absorption of insulin in rabbits in vitro and in vivo
JP3805975B2 (en) Wound healing agent
RU2004234C1 (en) Composition stimulating epithelium regeneration
Baluda et al. The effects of administration of drugs influencing haemostasis during treatment of patients with burns
KR100372672B1 (en) Compositions and methods useful for the prevention and treatment of endotoxin-related diseases
Gundersen et al. N-Acetylcysteine administered as part of the immediate post-traumatic resuscitation regimen does not significantly influence initiation of inflammatory responses or subsequent endotoxin hyporesponsiveness
JPH083065A (en) Therapeutic agent for hepatopathy
JPH028768B2 (en)
BG65654B1 (en) Method of obtaining microfibrillar water-soluble collagen for the food and pharmaceutical industries and cosmetics

Legal Events

Date Code Title Description
A201 Request for examination
N231 Notification of change of applicant
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20120131

Year of fee payment: 10

LAPS Lapse due to unpaid annual fee