WO1993010817A1 - CDw52-SPECIFIC ANTIBODY FOR TREATMENT OF MULTIPLE SCLEROSIS - Google Patents

CDw52-SPECIFIC ANTIBODY FOR TREATMENT OF MULTIPLE SCLEROSIS Download PDF

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Publication number
WO1993010817A1
WO1993010817A1 PCT/GB1992/002252 GB9202252W WO9310817A1 WO 1993010817 A1 WO1993010817 A1 WO 1993010817A1 GB 9202252 W GB9202252 W GB 9202252W WO 9310817 A1 WO9310817 A1 WO 9310817A1
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Prior art keywords
antibody
treatment
multiple sclerosis
campath
cdw52
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PCT/GB1992/002252
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French (fr)
Inventor
Geoffrey Hale
Herman Waldmann
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Individual
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Priority to DK92924783T priority Critical patent/DK0616537T3/en
Priority to CA002124964A priority patent/CA2124964C/en
Priority to KR1019940701885A priority patent/KR100271333B1/en
Priority to EP92924783A priority patent/EP0616537B1/en
Priority to DE69228556T priority patent/DE69228556T2/en
Priority to US08/244,316 priority patent/US6120766A/en
Application filed by Individual filed Critical Individual
Priority to HK98112902.5A priority patent/HK1011618B/en
Priority to JP50997393A priority patent/JP3383303B2/en
Publication of WO1993010817A1 publication Critical patent/WO1993010817A1/en
Anticipated expiration legal-status Critical
Priority to GR990400767T priority patent/GR3029683T3/en
Priority to US10/938,874 priority patent/US20050118172A1/en
Ceased legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/56—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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2893—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against CD52
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Definitions

  • the present invention relates to a method of treatment of certain auto-immune conditions in a human or animal subject.
  • the cells and molecules in an animal body do not normally stimulate an adaptive immune response in that body as a result of a number of mechanisms which ensure a state referred to as "self-tolerance". However, in certain circumstances these mechanisms may fail to prevent the stimulation of such an immune response and this condition is referred to as "auto-immunity".
  • auto-immunity A number of diseases in humans and animals are now thought to result from auto- immunity.
  • Multiple sclerosis is a demyelinating disease of the central nervous system the onset of which generally occurs within ' the age range from about 15 to 45.
  • Myelin is a fatty substance which forms a sheath around certain nerve fibres and which conducts nervous impulses at a rate which enables muscles to make precise and delicate movements.
  • the disease is characterised by induration of the sheath substance leading to the formation of plaques of varying size and location which interfere with the impulses normally conducted by the sheath.
  • the course of the disease can be highly variable in individual patients and may be subject to periods of spontaneous remission. However, the disease generally results in progressive deterioration of the control of muscle function with ultimate paralysis in many cases.
  • the precise cause of multiple sclerosis is unknown and it may result from a complex interaction of a number of different factors. However, it is now generally recognised that there is at least an autoimmune component in the causation of the disease.
  • the CDw52 antigen (a 23kDa glycoprotein also referred to as CAMPATH-l) is strongly expressed on the surface of all human lymphocytes and most monocytes but is absent from other blood cells including stem cells.
  • CAMPATH-l The CDw52 antigen
  • a number of antibodies have been developed directed against CDw52 which is an unusually good target for complement-mediated attack.
  • Antibodies against CDw52 bind to all lymphocytes and monocytes but lyse only lymphocytes (T and B) jln vivo. Antigens similar to CDw52 are expressed in other mammalian species.
  • CAMPATH-1M is a rat IgM monoclonal antibody which has been used extensively in vitro for purging bone marrow harvests in order to deplete the T cell population prior to bone marrow transplantation. Marked reduction in the incidence and severity of graft-versus-host disease has been seen with this therapy.
  • CAMPATH-1G is a rat IgG2b class-switch variant of an IgG2a antibody recognising the CDw52 antigen which has been used in vivo to achieve i itvunosupression in more than 100 patients undergoing organ and bone marrow transplantation, management of organ rejection and treatment of haematologic malignancies with a high level of success.
  • the rapid development of an anti-rat immunoglobulin response including the possibility of anaphylaxis, is likely to limit the use of rat monoclonal antibodies against the CDw52 antigen in humans in . vivo.
  • CAMPATH-1H is a genetically manipulated IgG antibody obtained by grafting the complementarity determining regions from CAMPATH-1G into human framework regions.
  • the resulting "humanized" antibody is highly effective in vitro being equivalent to the rat monoclonal antibody at complement lysis and two to four times better in cell- mediated lysis of human lymphocytes. No limiting anti- globulin response is anticipated with this humanized antibody.
  • Expression of CAMPATH-1H was achieved initially in rat myeloma cells by placing DNA encoding the engineered antibody chains in genomic context under control of the immunoglobulin promoter/enhancer.
  • CAMPATH-1H has recently been expressed to high levels in Chinese hamster ovary (CHO) cells. It has now surprisingly been found that antibodies against the CDw52 antigen may be effective in the treatment of multiple sclerosis.
  • the present invention provides a method of treatment of a human subject suffering from multiple sclerosis which comprises administering to the said subject an effective amount of an antibody recognising the CDw52 antigen.
  • the present invention also provides the use of an antibody recognising the CDw52 antigen for the manufacture of a medicament for the treatment of multiple sclerosis. It ' is preferred to use an anti-CDw52 antibody which does not carry with it the risk of the development of an immune reaction against the anti-body itself. Accordingly whilst it is possible to use mouse or rat mono-clonal antibodies it is preferred to use antibodies which have been produced by recombinant DNA technology and which have been engineered to reduce the risk of causing an immune reaction. Thus it is possible to use a chimeric antibody in which the constant domains of a mouse or rat anti-CDw52 antibody have been replaced by the constant domains of a human antibody.
  • a humanized or CDR-grafted antibody for the treatment of humans, i.e. an antibody in which the complementarity determining regions from a mouse or rat antibody are combined with framework regions and constant domains from one or more human antibodies.
  • the method according to the invention is carried out using the CDR-grafted antibody CAMPATH-1H (see Riechmann et a ⁇ , Nature, 322 , 323-327 (1988)) .
  • the antibody CAMPATH-1H can be produced in rat myeloma cells as originally described or it can be produced in any other expression system, particularly an expression system suitable for the production of a correctly folded, glycosylated, mammalian protein.
  • High yields of CAMPATH-1H have been obtained by expression in a genetically manipulated CHO cell line (Page and Sydenha , Biotechnology, 9 . , 64-68 (1991)) .
  • the dosages of anti-CDw52 antibody, preferably CAMPATH-1H, to be administered to a patient suffering from multiple sclerosis v/ill vary with the precise nature of the condition being treated and the recipient of the treatment.
  • the dose will generally be in the range 1 to about lOOmg for an adult patient, usually administered daily for a period between 1 and 30 days.
  • the preferred daily dose is 1 to lOmg per day although in some instances larger doses of up to 40mg per day may be used.
  • the anti-CDw52 antibody, particularly CAMPATH-1H will generally be administered to the patient in the form of a pharmaceutical formulation.
  • Such formulations preferably include, in addition to the antibody, a physiologically acceptable carrier or diluent, possibly in admixture with one or more other agents such as other antibodies or drugs, such as an antibiotic.
  • Suitable carriers include, but are not limited to, physiological saline, phosphate buffered saline, phosphate buffered saline glucose and buffered saline.
  • the antibody may be lyophilised (freeze dried) and reconstituted for use when needed by the addition of an aqueous buffered solution as described above.
  • Routes of administration are routinely parenteral, including intravenous, intramuscular, subcutaneous and intraperitoneal injection or delivery.
  • the anti-CDw52 antibody may be administered in combination with or sequentially with other drugs, in particular other drugs conventionally used in the treatment of multiple sclerosis, such as steroids, for example hydrocortisones such as methyl prednisolone, or other medicaments for the alleviation of specific symptoms of the disease. Sequential administration of the antibody with another drug may be appropriate in some cases.
  • the invention is illustrated by the following case history of a patient treated with the CDR-grafted anti- CDw52 antibody CAMPATH-1H.
  • the antibody used was produced by expression in a recombinant CHO cell line (Page and Sydenham, Biotechnology, 9 . , 64-68 (1991)) followed by extraction from the cell culture medium and purification.
  • the patient was a 43 year old female who sought medical attention after 10 days of progressive loss of sensation in her perineum. She had also experienced several episodes of urinary and fecal incontinence. Clinical evaluations were remarkable for normal visual evoked responses, multiple white matter abnormalities in the cerebral hemishperes identified by brain MRI, and oligoclonal bands in the CSF; a diagnosis of multiple sclerosis was made.
  • CAMP TH-1H (2 mg/day iv for five days, two days rest, then 10 mg/day iv for five days) .
  • Lymphocyte depletion was rapid, falling to 0.2 x 10 9 cells/L on the second dosing day from a pretreatment value of 3.8 x 10 9 cells/L. Lymphocyte counts remained less than 0.3 x 10 9 for approximately one month and then rose slowly to a value of 1.07 x 10 9 cells/L three months after treatment.
  • CRP within normal limits prior to treatment, increased to 140 mg/L, fell, and increased again to 91 mg/L on dosing days three and nine, respectively.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Biochemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Genetics & Genomics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Transplantation (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Peptides Or Proteins (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

The invention relates to the use of an antibody recognising the CDw52 antigen in the treatment of multiple sclerosis. Preferably the antibody is the humanised antibody in the humanised antibody CAMPATH-1H.

Description

CD 52 - SPECIFIC ANTIBODY FOR TREATMENT OF MULTIPLE SCLEROSIS
The present invention relates to a method of treatment of certain auto-immune conditions in a human or animal subject. The cells and molecules in an animal body do not normally stimulate an adaptive immune response in that body as a result of a number of mechanisms which ensure a state referred to as "self-tolerance". However, in certain circumstances these mechanisms may fail to prevent the stimulation of such an immune response and this condition is referred to as "auto-immunity". A number of diseases in humans and animals are now thought to result from auto- immunity.
Multiple sclerosis is a demyelinating disease of the central nervous system the onset of which generally occurs within' the age range from about 15 to 45. Myelin is a fatty substance which forms a sheath around certain nerve fibres and which conducts nervous impulses at a rate which enables muscles to make precise and delicate movements. The disease is characterised by induration of the sheath substance leading to the formation of plaques of varying size and location which interfere with the impulses normally conducted by the sheath. The course of the disease can be highly variable in individual patients and may be subject to periods of spontaneous remission. However, the disease generally results in progressive deterioration of the control of muscle function with ultimate paralysis in many cases. The precise cause of multiple sclerosis is unknown and it may result from a complex interaction of a number of different factors. However, it is now generally recognised that there is at least an autoimmune component in the causation of the disease.
The CDw52 antigen (a 23kDa glycoprotein also referred to as CAMPATH-l) is strongly expressed on the surface of all human lymphocytes and most monocytes but is absent from other blood cells including stem cells. A number of antibodies have been developed directed against CDw52 which is an unusually good target for complement-mediated attack. Antibodies against CDw52 bind to all lymphocytes and monocytes but lyse only lymphocytes (T and B) jln vivo. Antigens similar to CDw52 are expressed in other mammalian species.
Antibodies which have been developed against CDw52 and which have been used in therapy include the following: CAMPATH-1M is a rat IgM monoclonal antibody which has been used extensively in vitro for purging bone marrow harvests in order to deplete the T cell population prior to bone marrow transplantation. Marked reduction in the incidence and severity of graft-versus-host disease has been seen with this therapy.
CAMPATH-1G is a rat IgG2b class-switch variant of an IgG2a antibody recognising the CDw52 antigen which has been used in vivo to achieve i itvunosupression in more than 100 patients undergoing organ and bone marrow transplantation, management of organ rejection and treatment of haematologic malignancies with a high level of success. However, the rapid development of an anti-rat immunoglobulin response, including the possibility of anaphylaxis, is likely to limit the use of rat monoclonal antibodies against the CDw52 antigen in humans in. vivo.
CAMPATH-1H is a genetically manipulated IgG antibody obtained by grafting the complementarity determining regions from CAMPATH-1G into human framework regions. The resulting "humanized" antibody is highly effective in vitro being equivalent to the rat monoclonal antibody at complement lysis and two to four times better in cell- mediated lysis of human lymphocytes. No limiting anti- globulin response is anticipated with this humanized antibody. Expression of CAMPATH-1H was achieved initially in rat myeloma cells by placing DNA encoding the engineered antibody chains in genomic context under control of the immunoglobulin promoter/enhancer. CAMPATH-1H has recently been expressed to high levels in Chinese hamster ovary (CHO) cells. It has now surprisingly been found that antibodies against the CDw52 antigen may be effective in the treatment of multiple sclerosis.
The present invention provides a method of treatment of a human subject suffering from multiple sclerosis which comprises administering to the said subject an effective amount of an antibody recognising the CDw52 antigen.
The present invention also provides the use of an antibody recognising the CDw52 antigen for the manufacture of a medicament for the treatment of multiple sclerosis. It 'is preferred to use an anti-CDw52 antibody which does not carry with it the risk of the development of an immune reaction against the anti-body itself. Accordingly whilst it is possible to use mouse or rat mono-clonal antibodies it is preferred to use antibodies which have been produced by recombinant DNA technology and which have been engineered to reduce the risk of causing an immune reaction. Thus it is possible to use a chimeric antibody in which the constant domains of a mouse or rat anti-CDw52 antibody have been replaced by the constant domains of a human antibody. However, it is preferred to use a humanized or CDR-grafted antibody for the treatment of humans, i.e. an antibody in which the complementarity determining regions from a mouse or rat antibody are combined with framework regions and constant domains from one or more human antibodies.
Most preferably the method according to the invention is carried out using the CDR-grafted antibody CAMPATH-1H (see Riechmann et a∑, Nature, 322 , 323-327 (1988)) . As noted above, the antibody CAMPATH-1H can be produced in rat myeloma cells as originally described or it can be produced in any other expression system, particularly an expression system suitable for the production of a correctly folded, glycosylated, mammalian protein. High yields of CAMPATH-1H have been obtained by expression in a genetically manipulated CHO cell line (Page and Sydenha , Biotechnology, 9., 64-68 (1991)) .
The dosages of anti-CDw52 antibody, preferably CAMPATH-1H, to be administered to a patient suffering from multiple sclerosis v/ill vary with the precise nature of the condition being treated and the recipient of the treatment. The dose will generally be in the range 1 to about lOOmg for an adult patient, usually administered daily for a period between 1 and 30 days. The preferred daily dose is 1 to lOmg per day although in some instances larger doses of up to 40mg per day may be used. The anti-CDw52 antibody, particularly CAMPATH-1H will generally be administered to the patient in the form of a pharmaceutical formulation. Such formulations preferably include, in addition to the antibody, a physiologically acceptable carrier or diluent, possibly in admixture with one or more other agents such as other antibodies or drugs, such as an antibiotic. Suitable carriers include, but are not limited to, physiological saline, phosphate buffered saline, phosphate buffered saline glucose and buffered saline. Alternatively the antibody may be lyophilised (freeze dried) and reconstituted for use when needed by the addition of an aqueous buffered solution as described above. Routes of administration are routinely parenteral, including intravenous, intramuscular, subcutaneous and intraperitoneal injection or delivery. The anti-CDw52 antibody may be administered in combination with or sequentially with other drugs, in particular other drugs conventionally used in the treatment of multiple sclerosis, such as steroids, for example hydrocortisones such as methyl prednisolone, or other medicaments for the alleviation of specific symptoms of the disease. Sequential administration of the antibody with another drug may be appropriate in some cases.
The invention is illustrated by the following case history of a patient treated with the CDR-grafted anti- CDw52 antibody CAMPATH-1H. The antibody used was produced by expression in a recombinant CHO cell line (Page and Sydenham, Biotechnology, 9., 64-68 (1991)) followed by extraction from the cell culture medium and purification.
It is to be understood that the following case history is not intended to be in any way limiting on the scope of the invention. CASE HISTORY
The patient was a 43 year old female who sought medical attention after 10 days of progressive loss of sensation in her perineum. She had also experienced several episodes of urinary and fecal incontinence. Clinical evaluations were remarkable for normal visual evoked responses, multiple white matter abnormalities in the cerebral hemishperes identified by brain MRI, and oligoclonal bands in the CSF; a diagnosis of multiple sclerosis was made.
Treatment with high-dose iv ethylprednisolone induced an incomplete recovery (decreased incontinence with continued perineal numbness and stiff legs) . Four months after initially seeking medical attention, the patient had an episode of left-sided facial pain and left leg numbness consistent with brainstem de yelination. Over the next twelve months symptoms gradually worsened and at the end of this period the patient was admitted to hospital with left optic neuritis and Lhermitte's phenomenon. A second course of iv methylprednisolone (500 mg/day for five days) was associated with limited improvement. The disease was judged to have entered a chronic progressive phase and over the next few months the patient suffered further identifiable episodes of brainstem demyelination and left optic neuritis.
Twenty months after she initially sought medical attention, the patient received treatment with CAMP TH-1H (2 mg/day iv for five days, two days rest, then 10 mg/day iv for five days) . Lymphocyte depletion was rapid, falling to 0.2 x 109 cells/L on the second dosing day from a pretreatment value of 3.8 x 109 cells/L. Lymphocyte counts remained less than 0.3 x 109 for approximately one month and then rose slowly to a value of 1.07 x 109 cells/L three months after treatment. CRP, within normal limits prior to treatment, increased to 140 mg/L, fell, and increased again to 91 mg/L on dosing days three and nine, respectively. This "double-peaked" pattern was also seen with neutrophils which increased during the same time course and coincided with the second and third dosing days at 2 and 10 mg respectively (10 mg doses followed a two day rest) . Disease activity was not significantly altered during or immediately following CAMPATH-1H treatment. Kurtzke neurological status at approximately one and two months after initiation of treatment was improved to a composite score of 11 from a pretreatment score of 14. A second rating system for scoring disease activity in demyelinating disease also documented improvement in the progression, disability and relapse assessment categories.
The 10 dose CAMPATH-1H treatment course was well tolerated. Fever and headache were reported as adverse events with both occurring with administration of the first 2 mg and 10 mg doses. Also reported was transient left- sided visual disturbance on day three, the significance of which was unclear in the light of the pre-existing left optic neuritis. Approximately 18 months after the treatment with
CAMP TH-IH, the improvement in the condition of the patient had been maintained.

Claims

CLAIMS :
1. The use of an antibody recognising the CDw52 antigen for the manufacture of a medicament for the treatment of multiple sclerosis.
2. The use according to Claim 1 wherein the antibody is a humanised antibody, including CDRs from a mouse or rat antibody combined with framework regions and constant domains from one or more human antibodies.
3. The use according to Claim 2 wherein the antibody is CAMPATH-IH.
4. The use according to any of Claims 1 to 3 wherein the treatment involves daily administration to a patient of a dose of from 1 to 10 mg per day for a period of 1 to 30 days.
5. The use according to any of Claims 1 to 4 wherein the treatment includes administration of a steroid.
6. A therapeutic agent for the treatment of multiple sclerosis comprising an antibody recognising the CDw52 antigen as the active ingredient.
7. A therapeutic agent according to Claim 6 wherein the antibody is a humanised antibody including CDRs from a mouse or rat antibody combined with framework regions and constant domains from one or more human antibodies.
8. A therapeutic agent according to Claim 7 wherein the antibody is CAMPATH-IH.
A therapeutic agent according to any of Claims 6 to 8 wherein the daily dose of the antibody is from 1 to 10 mg per day for a period of 1 to 30 days.
10. A therapeutic agent as claimed in any of Claims 6 to 9 wherein the treatment includes administration of a steroid.
11. A method for the treatment of a human subject suffering from multiple sclerosis which comprises administering to the said subject an effective amount of an antibody recognising the CDw52 antigen.
12. A method according to claim 11 wherein the antibody is a humanised antibody including CDRs from mouse or rat antibody combined with framework regions and constant domains from one or more human antibodies.
13. A method according to Claim 12 wherein the antibody is CAMPATH-IH.
14. A method according to any of Claims 11 to 13 which comprises daily administration of the antibody at a dose of from 1 to 10 mg per day for a period of 1 to 30 days.
15. A method according to any of Claims 11 to 14 which includes administration of an effective amount of a steroid.
PCT/GB1992/002252 1991-12-04 1992-12-04 CDw52-SPECIFIC ANTIBODY FOR TREATMENT OF MULTIPLE SCLEROSIS Ceased WO1993010817A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
HK98112902.5A HK1011618B (en) 1991-12-04 1992-12-04 Cdw52-specific antibody for treatment of multiple sclerosis
CA002124964A CA2124964C (en) 1991-12-04 1992-12-04 Cdw52-specific antibody for treatment of multiple sclerosis
KR1019940701885A KR100271333B1 (en) 1991-12-04 1992-12-04 Cdw-52 specific antibody for treatment of multiple sclerosis
EP92924783A EP0616537B1 (en) 1991-12-04 1992-12-04 CDw52-SPECIFIC ANTIBODY FOR TREATMENT OF MULTIPLE SCLEROSIS
DE69228556T DE69228556T2 (en) 1991-12-04 1992-12-04 CDw52-SPECIFIC ANTIBODIES FOR TREATING MULTIPLE Sclerosis
DK92924783T DK0616537T3 (en) 1991-12-04 1992-12-04 CDw52-specific antibody for the treatment of disseminated sclerosis
JP50997393A JP3383303B2 (en) 1991-12-04 1992-12-04 CDw52-specific antibodies for the treatment of multiple sclerosis
US08/244,316 US6120766A (en) 1991-12-04 1992-12-04 CDW52-specific antibody for treatment of multiple sclerosis
GR990400767T GR3029683T3 (en) 1991-12-04 1999-03-12 CDw52-SPECIFIC ANTIBODY FOR TREATMENT OF MULTIPLE SCLEROSIS.
US10/938,874 US20050118172A1 (en) 1991-12-04 2004-09-13 CDw52-specific antibody for treatment of multiple sclerosis

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB919125768A GB9125768D0 (en) 1991-12-04 1991-12-04 Therapeutic method
GB9125768.3 1991-12-04

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US61382300A Continuation 1991-12-04 2000-07-11

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US (2) US6120766A (en)
EP (1) EP0616537B1 (en)
JP (1) JP3383303B2 (en)
KR (1) KR100271333B1 (en)
AT (1) ATE177011T1 (en)
AU (1) AU3089692A (en)
CA (1) CA2124964C (en)
DE (1) DE69228556T2 (en)
DK (1) DK0616537T3 (en)
ES (1) ES2128363T3 (en)
GB (1) GB9125768D0 (en)
GR (1) GR3029683T3 (en)
IL (1) IL103981A (en)
MX (1) MX9207032A (en)
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US5545405A (en) * 1990-10-17 1996-08-13 Burroughs Wellcome Co. Method for treating a mammal suffering from cancer with a cho-glycosylated antibody
WO1997031024A1 (en) * 1996-02-20 1997-08-28 Isis Innovation Limited Antibody variants
WO2003059387A3 (en) * 2001-12-21 2004-06-17 Ilex Oncology Inc Combination comprising anti-cd52 antibodies and other therapeutic agents for treatment for multiple sclerosis
WO2005042581A3 (en) * 2003-11-01 2005-07-28 Biovation Ltd Modified anti-cd52 antibody
EP2444104A3 (en) * 2006-09-13 2012-10-24 Alcafleu Management GmbH & Co. KG Treatment of multiple sclerosis (MS) with campath-1H
US8669352B2 (en) 2006-05-09 2014-03-11 Fast Forward Pharmaceuticals B.V. Antagonistic anti-human CD40 monoclonal antibody
US9498528B2 (en) 2006-09-13 2016-11-22 Genzyme Corporation Treatment of multiple sclerosis (MS)

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AU2003216436A1 (en) * 2002-02-08 2003-09-02 Life Technologies Corporation Compositions and methods for restoring immune responsiveness in patients with immunological defects
WO2004003142A2 (en) 2002-06-28 2004-01-08 Xcyte Therapies, Inc. Compositions and methods for restoring immune repertoire in patients with immunological defects related to autoimmunity and organ or hematopoietic stem cell transplantation
EP1623017B1 (en) * 2003-05-08 2010-09-15 Life Technologies Corporation Generation and isolation of antigen-specific t cells
CA2539716A1 (en) * 2003-09-22 2005-04-07 Xcyte Therapies, Inc. Compositions and methods to accelerate hematologic recovery
EP2016095A2 (en) 2006-04-13 2009-01-21 Peptimmune, Inc. Methods for designing and synthesizing directed sequence polymer compositions via the directed expansion of epitope permeability
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