WO2005117902A1 - Combination therapy with glatiramer acetate and minocycline for the treatment of multiple sclerosis - Google Patents
Combination therapy with glatiramer acetate and minocycline for the treatment of multiple sclerosis Download PDFInfo
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- WO2005117902A1 WO2005117902A1 PCT/US2005/018938 US2005018938W WO2005117902A1 WO 2005117902 A1 WO2005117902 A1 WO 2005117902A1 US 2005018938 W US2005018938 W US 2005018938W WO 2005117902 A1 WO2005117902 A1 WO 2005117902A1
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- minocycline
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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
- A61K31/74—Synthetic polymeric materials
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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
- A61K31/60—Salicylic acid; Derivatives thereof
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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
- A61K31/65—Tetracyclines
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/02—Peptides of undefined number of amino acids; Derivatives thereof
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
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- 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
Definitions
- the subject invention relates to combination therapy for treating multiple sclerosis.
- multiple sclerosis This condition is a chronic, inflammatory CNS disease characterized pathologically by demyelination.
- CNS disease characterized pathologically by demyelination.
- RR-MS relapsing-remitting multiple sclerosis
- SP-MS secondary progressive multiple sclerosis
- PP-MS primary progressive multiple sclerosis
- PR-MS progressive-relapsing multiple sclerosis
- Be ign multiple sclerosis may, however, progress into other f.orms of- multiple sclerosis.
- Patients suffering from RR-MS experience sporadic exacerbations or relapses, as well as periods of remission. Lesions and evidence of axonal loss may or may not be visible on MRI for patients with RR-MS.
- SP-MS may evolve from RR-MS. Patients afflicted with SP-MS have relapses, a diminishing degree of recovery during remissions, less frequent remissions and more pronounced neurological deficits than RR-MS pat ' ients . Enlarged ventricles, which are markers for atrophy of the corpus callosum, midline center and spinal cord, are visible on MRI of patients with SP-MS.
- PP-MS is characterized by a steady progression of increasing neurological deficits without distinct attacks or remissions. Cerebral lesions, diffuse spinal cord damage and evidence ' of axonal loss are evident on the MRI of patients with PP-MS. PR-MS has periods of acute exacerbations while proceeding along a course of increasing neurological deficits without remissions. Lesions are evident on MRI of patients suffering from PR-MS (Multiple sclerosis: its diagnosis, symptoms, types and stages, 2003 ⁇ http: //www. albany.net/ ⁇ tjc/multiple-sclerosis .html>) .
- EAE allergic encephalomyelitis
- TMEV Theiler' s murine encephalomyelitis virus
- Animal model Theiler' s virus infection in mice, Am. J. Pa th . 88:497-500, 1977; Rodriguez, et al . , Theiler' s murine encephalomyelitis: a model of demyelination and persistence of virus, Crit . Rev. Immunol . , 7:325, 1987), supports the theory that a foreign agent initiates multiple sclerosis.
- injection of the virus results in spinal cord demyelination.
- Glatiramer acetate also known as Copolymer-1, has .been shown to be effective in treating multiple sclerosis (MS) (Lampert, Autoimmune and virus-induced demyelinating diseases. A review, Am. J. Path .-, 91:176-208, 1978; Martyn, The epidemiology of multiple sclerosis in McAlpine's Multiple Sclerosis, Matthews, B., ed., London: Churchil Livingstone, 3-40, 1991).
- MS multiple sclerosis
- COPAXONE® is the brand name for a formulation containing glatiramer acetate as the active ingredient. Glatiramer acetate is approved for reducing the frequency of relapses in relapsing- remitting multiple sclerosis. Glatiramer acetate consists of the acetate salts of synthetic polypeptides containing four naturally occurring amino acids: L-glutamic acid, L-alanine, L- tyrosine, and L-lysine with an average molar fraction in COPAXONE® of 0.141, 0.427, 0.095 and 0.338, respectively. In COPAXONE®, the average molecular weight of the glatiramer acetate is 4,700-11,000 daltons .
- glatiramer acetate is designated L-glutamic acid polymer with L-alanine, L-lysine and L-tyrosine, acetate (salt). Its structural formula is: ( Glu , Ala , Lys , Tyr ) x -CH 3 COOH ( C 5 H 9 N0 4 -C 3 H 7 N0 2 -C6H ⁇ 4 N 2 0 2 -C 9 H ⁇ N0 3 ) ⁇ - ⁇ C 2 H 4 0 2
- the recommended dosing schedule of COPAXONE® for relapsing- remitting .multiple sclerosis is 20 mg per' day injected
- GA In rodents, GA suppresses the encephalitogenic effects of auto reactive T-cells. Passive transfer of GA-reactive T-cells prevents the development of EAE induced in rats or mice by MBP, protolipid protein (PLP) or Myelin Oligodendrocyte Glycoprotein (MOG) (Aharoni, D., et al., T-suppressor hybridomas and interleukin-2-dependent lines induced by copolymer-1 or by spinal cord homogenate down-regulate experimental allergic encephalomyelitis. Eur. J. Immunol .
- BDNF Brain Derived Neurotrophic Factor
- GA has a dual mechanism of action. It is a unique immunomodulating agent that stimulates Th2 cells to secrete both anti-inflammatory cytokines as well as BDNF. This provides an anti-inflammatory milieu and. neurotrophic support to .the demyelinating axons protecting them from further degeneration over the long term.
- MRI Magnetic Resonance Imaging
- Minocycline is a semisynthetic derivative of tetracycline, named [4S- (4oc, 4acc, 5a°c, 12a ⁇ x) ] -4, 7-bis (dimethylamino) - 1,4, 4a, 5, 5a, 6, 11, 12a-octahydro-3, 10, 12, 12a-tetrahydroxy-l, 11- dioxo-2-naphthacenecarboxamide . Its structural formula is:
- Minocycline is a tetracycline with antibacterial activity comparable to other tetracyclines with activity against a wide range of gram-negative and gram-positive organisms.
- the usual dosage and frequency of administration of minocycline differs from that of the other tetracyclines.
- the usual adult dosage of minocycline is 200 mg initially followed by 100 mg every, 12 hours.
- the usual dosage of minocycline is 4 mg/kg initially followed by 2 g/kg every 12 hours ("MINOCIN®" in Physician's Desk Reference, Medical Economics Co., Inc., Montvale, NJ, 2003, 3420-3424).
- Minocycline is commercially available . as minoycline hydrochloride, C 23 H 27 N 3 0 , which has a molecular weight of 493,94, in a capsule under the tradename, DYNACIN®. Minocycline hydrochloride is also available under the tradename, MINOCIN®, as an oral suspension, a pellet-filled capsule or an intravenous preparation. ' However, the labeling for MINOCIN® intravenous specifically warns that parenteral therapy is indicated only when oral therapy is not adequate or tolerated. Oral therapy should be instituted as soon as possible. If intravenous therapy is given over prolonged periods of time, thrombophlebitis may result ("DYNACIN®" in Physician's Desk Reference, Medical Economics Co., Inc., Montvale, NJ, 2003, 1921-1923).
- Minocycline has a wide range of immunomodulatory properties. When tested against EAE, minocycline has been, confirmed to dramatically suppress disease activity in chronic relapsing remitting EAE (Popovic et al., Inhibition of autoimmune encephalomyelitis by a tetracycline. Ann i7euro2, 51: 215-223, 2002), to delay the course of severe EAE, and attenuate the severity of mild EAE (Brundula et al., Targeting leukocytes MMPs and transmigration: Minocycline as a potential therapy for multiple sclerosis, Brain 125: 1297-1308, 200
- minocycline suppresses clinical disease and histopatological evidence of inflammation within the CNS and prevents microglial activation and demyelination.
- the efficacy of minocycline in EAE is not thought to be due to its anti-microbial activity but rather due to some of its other reported actions, including the inhibition of production and activity of matrix metalloproteinases (Brundula) , lowering of levels Of various cytokines (Yrjanheikki, et al . , A tetracycline derivative, minocycline, reduces inflammation and protects against focal cerebral ischemia with a wide therapeutic window.
- Proc Natl Acad Sci USA, 96: 13496-13500 1999; Tikka T., et al .
- Minocycline provides neuroprotection against N-methyl-D-aspartate neurotoxicity by inhibiting microglia.
- minocycline has not been tested in combination with glatiramer acetate.
- glatiramer acetate and minocycline are effective in combination to treat a form of multiple sclerosis, specifically, relapsing-remitting multiple sclerosis.
- the subject invention provides a method of treating a subject afflicted with a form of multiple sclerosis comprising periodically administering to the subject an amount of glatiramer acetate and an amount of minocycline, wherein the amounts when taken together are effective to alleviate a symptom of the form of multiple sclerosis in the subject so as to thereby treat the subject.
- the subject invention further provides a pharmaceutical composition comprising an amount of glatiramer acetate and an amount of minocycline, wherein the amounts wlfien taken together are effective to alleviate a symptom of a, form of multiple sclerosis in a subject.
- the subject invention provides a package comprising i) a first pharmaceutical composition comprising an amount of glatiramer acetate and a pharmaceutically acceptable carrier; ii) a second pharmaceutical composition comprising an amount of minocycline and a pharmaceutically acceptable carrier; and iii) instructions for use of the first and second pharmaceutical compositions together to alleviate a symptom of a form of multiple sclerosis in a subject.
- Figure 1 shows a timeline for the administration of glatiramer acetate, minocycline, MOG, pertussis toxin in Experiments 1-2.
- Figure 2 shows the average group clinical scores for manifestations of EAE in Experiment 1.
- Figure 3 shows the sum of clinical .scores for EAE manifestations in Experiment 1.
- Figure 4 shows the average group clinical scores for EAE manifestations in Experiment 2.
- Figure 5 shows the sum of clinical scores for manifestations of EAE in Experiment 2.
- the subject invention provides a method of treating a subject afflicted with a form of multiple sclerosis comprising periodically administering to the subject an amount of glatiramer acetate and an amount of minocycline, wherein the amounts when taken together are effective to alleviate a symptom of the form of multiple sclerosis in the subject so as to thereby treat the subject.
- the form of multiple sclerosis is relapsing- remitting multiple sclerosis.
- the subject is a human being.
- each of the amount of glatiramer acetate when taken alone, and the amount of minocycline when taken alone is effective to alleviate the symptom of the form of multiple sclerosis.
- either the amount of glatiramer acetate when taken alone, the amount of minocycline when taken alone or each such amount when taken alone is not effective to alleviate the symptom of the form of multiple sclerosis.
- the symptom is the frequency of relapses, the frequency of clinical exacerbation, or the accumulation of physical disability.
- the amount of glatiramer acetate may be 10 to 80 mg; or 12 to 70 mg; or 14 to 60 g; or 16 to 50 mg; or 18 to 40 g; or 20 to 30 mg; or 20 mg .
- the amount of minocycline may be 50-200 mg; or 60-175 mg; or 70-150 g; or 80-125 mg; or 90-110 mg; or 95- 105 mg; or 100 mg.
- the amount of glatiramer acetate may be in the range from 10 to 600 g/week; or 100 to 550 mg/week; or 150 to 500 mg/week; or 200 to 450 mg/week; or 250 to 400 mg/week ; or 300 to 350 mg/week; or 300 mg/week.
- the amount of glatiramer acetate may be in the range from 50 to 150 g/day; or 60 to 140' g/day; or 70 to 130 mg/day; or 80 to 120 mg/day; or 90 to 110 mg/day; or 100 mg/day.
- the amount of glatiramer acetate may be in the range from 10 to 80 mg/day; or 12 to 70 mg/day; or 14 to 60 mg/day; or 16 to 50 mg/day; or 18 to 40 mg/day; or 19 to 30 mg/day; or 20 mg/day.
- the periodic administration of glatiramer acetate is effected daily.
- the periodic administration of glatiramer acetate is effected twice daily at one half the amount.
- the periodic administration of glatiramer acetate is effected once every 3 to 11 days; or once every 5 to 9 days; or once every 7 days; or once every 24 hours.
- the minocycline may be administered once every 6 to 24 hours ; or once every 7 to 22 hours; or once every 8 to 20 hours; or once every 9 to 18 hours; or once every 10 to 16 hours; or once every 11 to 14 hours; or once every 12 hours.
- the administration of the glatiramer acetate substantially precedes the administration of the minocycline.
- the administration of the minocycline substantially precedes the administration of the glatiramer acetate.
- the glatiramer acetate and the minocycline may be administered for a period of time of at least 4 days.
- the period of time may be 5 days to 5 years; or 10 days to 3 years; or 2 weeks to 1 year; or 1 month to 6 months; or 3 months to 4 months.
- the glatiramer acetate and the minocycline may be administered for the lifetime of the subject.
- minocycline or glatiramer acetate may each independently be oral, nasal, pulmonary, parenteral, intravenous, intra-articular, transdermal, intradermal, subcutaneous, topical, intramuscular, rectal, intrathecal, intraocular, buccal or by gavage.
- the preferred route of administration is oral or by gavage.
- the preferred route of administration for glatiramer acetate is subcutaneous or oral.
- doses at the higher end of the range may be required for oral administration.
- the administration of the glatiramer acetate may be subcutaneous, intraperitoneal, intravenous, intramuscular, intraocular or oral and the administration of the minocycline may be oral.
- the administration of the glatiramer acetate may be subcutaneous and the administration of the minocycline may be oral.
- the subject invention further provides a pharmaceutical composition comprising an amount of glatiramer acetate and an amount of minocycline, wherein the amounts when taken together are effective to alleviate a symptom of a form of multiple sclerosis in a subject.
- a pharmaceutical composition comprising an amount of glatiramer acetate and an amount of minocycline, wherein the amounts when taken together are effective to alleviate a symptom of a form of multiple sclerosis in a subject.
- each of the amount of glatiramer acetate when taken alone and the amount of minocycline when taken alone is effective to alleviate the symptom of multiple sclerosis.
- either of the amount of glatiramer acetate when taken alone, or the amount of minocycline when taken alone or each such amount when taken alone is not effective to alleviate the symptom of multiple sclerosis.
- the amount of glatiramer acetate may be in the range from 10 to 600 mg; or 100 to 550 mg; or 150 to 500 mg; or 200 to 450 mg; or 250 to 400 mg; or 300 to 350 mg; or 300 mg.
- the amount of glatiramer acetate may be in the range from 10 to 80 mg; or 12 to 70 mg; or 14 to 60 mg; or 16 to 50 mg; or 18 to 40 mg; or 19 to 30 mg; or 20 mg.
- the amount of glatiramer acetate in the pharmaceutical composition may be in the range from 50 to 150 mg; or 60 to 140 mg; or 70 to 130 mg; or 80 to 120 mg; or 90 to 110 mg; or 100 mg.
- the amount of minocycline in the pharmaceutical composition may be 50-200 mg; or 60-175 mg; or 70-150 mg; or 80- 125 mg; or 90-110 g; or 95-105 mg; or 100 mg.
- the subject invention also provides a package comprising i) a first pharmaceutical composition comprising an amount of glatiramer acetate and a pharmaceutically acceptable carrier; ii) a second pharmaceutical composition comprising an amount of minocycline " and a pharmaceutically acceptable carrier; and iii) instructions for use of the first and second pharmaceutical compositions together to alleviate a symptom of a form of multiple sclerosis in a subject.
- the amount of glatiramer acetate may be in the range from 10 to 600 g; or 100 to 550 mg; or 150 to 500 mg; or 200 to 450 mg; or 250 to 400 mg; or 300 to 350 mg; or 300 mg.
- the amount of glatiramer acetate may be in the range from 10 to 80 mg; ,or 12 to 70 mg; or I 1144 ttoo 60 g; or 16 to 50 mg; or 18 to 40 mg; or 19 to 30 g; or 20 mg.
- the amount of glatiramer acetate in the package may be in the range from 50 to 150 g; or 60 to 140 g; or 70 to 130 mg; or 80 to 120 mg; or 90 to 110 g; or 100 mg.
- the amount of minocycline in the package may be 50-200 g; or 60-175 g; or 70-150 mg; or 80-125 mg; or 90-110 mg; or 95-105 mg; or 100 mg.
- the subject invention further provides a pharmaceutical combination comprising separate dosage forms of an amount of glatiramer acetate and an amount of minocycline, which combination is useful to alleviate a symptom of a form of multiple sclerosis in a subject.
- each of the amount of glatiramer acetate when taken alone and the amount of minocycline when taken alone is effective to alleviate the symptom of multiple sclerosis.
- either of the amount of glatiramer acetate when taken alone, the amount of minocycline when taken alone or each such amount when taken alone is not effective to alleviate the symptom of multiple sclerpsis.
- the pharmaceutical combination may be for simultaneous, separate or sequential use to treat the form of multiple sclerosis in the subject.
- Formulations of the invention suitable for oral administration may be in the form of capsules, pills, tablets, powders, granules, or as a solution or a suspension in an aqueous or non- aqueous liquid, or as an oil-in-water or water-in-oil liquid emulsion, or as an elixir or syrup, or as pastilles (using an inert base, such as gelatin and glycerin, or sucrose and acacia) and/or as mouth washes and the like, each containing a predetermined amount of the active compound or compounds .
- an inert base such as gelatin and glycerin, or sucrose and acacia
- the active ingredient (s) is mixed with one or more pharmaceutically acceptable carriers, such as sodium citrate or dicalcium phosphate, and/or any of the following: fillers or extenders, such as starches, lactose, sucrose, glucose, mannitol, and/or silicic acid; binders, such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone, sucrose and/or acacia; humectant ⁇ , such as glycerol; disintegrating agents, such as agar-agar, calcium carbonate, calcium phosphate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate; solution retarding agents, such as paraffin; absorption accelerators, such as quaternary ammonium compounds; wetting agents, such as, for example, cetyl alcohol and
- compositions may also comprise buffering agents.
- Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugars, as well as high molecular weight polyethylene glycols and the like.
- Liquid dosage forms ' for oral administration of the active ingredients include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs.
- the lijquid dosage forms may contain inert dilutents commonly used in ; the art, such as, i for example, water or other solvents, solubilizing agents and emulsifiers, such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor and sesame oils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof.
- inert dilutents commonly used in ; the art, such as, i for example, water
- Suspensions in addition to the active compounds, may contain suspending agents such as ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof.
- suspending agents such as ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof.
- the pharmaceutical compositions may also include human adjuvants or carriers known to those skilled in the art.
- adjuvants include complete Freund's adjuvant and incomplete Freund' ⁇ adjuvant.
- the compositions may also comprise wetting agents, emulsifying and suspending agents, sweetening, flavoring, coloring, perfuming and preservative agents .
- Glatiramer acetate may be formulated into pharmaceutical compositions with pharmaceutically acceptable carriers, such as water or saline and may be formulated into eye drops.
- Glatiramer acetate may also be formulated into delivery systems, such as matrix systems .
- EXPERIMENT 1 EFFECT OF LOW DOSES OF GLATIRAMER ACTETATE AND MINOCYCLINE ON SEVERE EAE
- EAE In 12-week old C57/BL6 mice, EAE was induced by the use of a low dose of MOG (33-55 peptide) (50 ⁇ g) in complete Freund's adjuvant that was not supplemented with mycobacterium. This protocol resulted in mice with severe EAE.
- Copaxone® was administered to mice as a pre-treatment.
- Copaxone® was given as a single injection, 7 days before MOG immunizatiopi.
- Copaxone® was administered in incomplete Freund's 'adjuvant.
- a sub-optimal dose of Copaxone® 250 ⁇ g was used Intraperitoneal pertussis toxin was given on the day of MOG administration and also 2 days after.
- Figure 1 presents a layout of the experimental design.
- Minocycline was administered intraperitoneally at a sub-optimal dose (25 mg/kg) when the first mouse in the entire experiment developed signs of EAE (See Figure 1) . Minocycline was administered daily until mice were sacrificed.
- mice were employed in each group: 10 in the saline vehicle group, and 9 each in the other 3 groups (Copaxone® alone, minocycline alone and combination of Copaxone® and minocycline) .
- the scale of 0 to 5 that is normally used to assess the degree of disability of EAE is inadequate, since it does not take into account the fact that in many animals only 1 (rather than 2) of hind or fore limbs are involved, etc. Thus, there could be quite marked differences between 2 mice designated as Grade 2 EAE on the old. scale (no forelimb involvement yet): one mouse may have two hind limbs impaired, while the other mouse may have only 1 hind limb involved. Thus, we have developed a new system in order to better differentiate functional outcomes.
- the scale goes from 1 to 15 and is the sum of the state of the tail and of the 4 limbs.
- EXPERIMENT 2 EFFECT OF LOW DOSES OF GLATIRAMER ACTETATE AND MINOCYCLINE ON MODERATE EAE
- mice in each group was as follows: 8 in the vehicle group, 11 in the minocycline group, 10 in the Copaxone® group, and 9 in the combination group.
- mice Only 1 mouse, did not complete the trial and was excluded from analysis. This was saline vehicle mouse #7, which was found dead in the cage on Day 18 of the experiment. This mouse had been bloated for several days and death was presumed to be due to abdominal disturbances of unknown causes.
- This experiment is conducted to evaluate whether the combination of minocycline and "Copaxone® is more effective at decreasing T cell transmigration across a fibronectin-coated Boyden chamber in vi tro than either alone.
- T lymphocytes of over 90% purity are isolated from the blood of healthy volunteers.
- 3 ⁇ m pore size fibronectin-coated chambers are used.
- the bottom chamber contains AIM-V medium (serum-free GIBCO® medium) with 1% fetal calf serum (to provide a directional gradient) while 500,000 cells in AIM-V are added to the upper chamber.
- the purpose of this trial is to compare the treatment of participants with relapsing-remitting multiple sclerosis (RR-MS) with COPAXONE® in combination with-minocycline, with treatment with COPAXONE® in combination with placebo.
- the clinical objective is to evaluate the effect of treatments on MRI variables, clinical evaluations and immunological profile.
- the design of this trial is a randomized, double-masked, 2-arm study of COPAXONE® in combination with minocycline versus COPAXONE® in combination with placebo for the treatment of relapsing-remitting multiple sclerosis.
- Twenty patients with RRMS who meet the inclusion/exclusion criteria are enrolled per arm. Patients are randomized and receive either 20 mg SQ (subcutaneous), of COPAXONE® daily plus an oral dose of placebo daily or 20 mg SQ of COPAXONE® in combination with 100 mg oral minocycline every 12 hours .
- Participant inclusion criteria are as follows: 1) Subjects have clinically definite MS as defined by (Poser CM. et al . New diagnostic criteria for multiple sclerosis: Guidelines for research protocols. Ann. Neurol., 13(3): 227-31, 1983) with disease duration (from onset) of at least 6 months; 2) Subjects have a relapsing-remitting disease course; 3) Subjects have had at least 1 documented relapse within the last year prior to study entry; 4) Subjects have at least 1 and not more than 15 gadolinium (Gd) -enhancing lesions on the screening MRI scan; 5) Subjects must be relapse-free and not have taken corticosteroids (IV, IM and/or PO) within the 30 days prior to the screening visit; 6) Subjects may be male or female.
- Gd gadolinium
- Subjects are between the ages of 18 and 50 years inclusive; 8) Subjects are ambulatory, with a Kurtzke EDSS score of between 0 and 5 inclusive; and 9) Subjects must be willing and able to give written informed consent prior to entering the -study.
- Participant exclusion criteria include the following: 1 ) previous use of injectable glatiramer acetate; 2) previous use of cladribine; 3 ) previous use of immunosuppressive agents in the last 6 months; 4) use of experimental or investigational drugs, including I.v.
- immunoglobulin within
- Subjects appear for a study screening visit, and if they meet all inclusion criteria, they return within 28 days for the baseline visit. Subjects are randomized and receive their first dose of study medication at the baseline visit. Subjects return at months 1, 3, 6, 8 and 9. At the month 9 visit subjects are terminated from the study medication. The treatment duration is 9 months .
- Screening MRI must occur 10 days ⁇ 4 days prior to randomization and first dose.
- a month is defined as 28 days ⁇ 4 days
- the screening chest X-ray may be deferred if a chest X-ray has been performed in the 6 months prior to screening and a report is available. Should the report indicate abnormal findings, the chest x-ray must be repeated.
- a scheduled MRI is performed and not delayed.
- MRI-AC MRI Analysis Center
- Both the Treating and Examining neurologists remain blinded to the results of all MRI scans. The only exception is that the screening MRI scan may be reviewed by the Treating neurologist to determine if a patient meets inclusion criteria. However, patients are not randomized into the trial until the MRI Analysis Center confirms the screening MRI is received in acceptable condition and the patient meets MRI inclusion criteria .
- the primary end-point for this study is the total number of enhancing lesions measured at months 8 and 9.
- the analysis of this end-point utilizes the Quasi-Likelihood (over-dispersed)
- Offset based on the log of exposure. Screening lesion count is i used as a covariate. Treatment arid center effects are included in the model. The center-by-treatment interaction term is tested using the -2 log likelihood ratio test. The treatment-by-center interaction is included in the principal analysis model if it is found to be statistically significant (i.e. if p->0.10).
- the Hierarchy Approach is used to control for multiplicity, resulting from the planned secondary end-points significance testing.
- the secondary endpoints given in the hierarchical order of the statistical analysis are outlined below.
- Secondary outcome assessments compare the two study groups in MRI parameters as measured at months 8 and 9 visits: 1) the total number of new Tl Gd-enhancing lesions.; 2) the total number of new T2 lesions; and 3) the change from baseline to termination in total volume of T2 lesions.
- the number of new lesions of MRI scans counted in month 9, with reference to the previous scan, is analyzed similarly to the primary endpoint.
- the change from baseline to termination in total volume of T2 lesions is analyzed applying the Analysis of Covariance (ANCOVA, SAS.
- the model includes the following fixed effects: treatment group, center and baseline volume easurement.
- the treatment-by-center interaction is included in the model if it is found to be statistically significant (i.e. if p ⁇ 0.10).
- Rank transformation is implemented to the volume changes in case of significant (i.e. if p ⁇ 0.001 - Shapiro-Wilk's test) deviation from normality.
- Exploratory outcome assessments compare the two study groups in the following parameters: 1) the number of ew lesions (Gd- enhancing and/or new PD/T2 lesions) identified at month 1 (compared to screening) and month 3 (compared to month 1) which become persistent/chronic Tl hypointensities (black holes) at month 9; 2) Treatment effect evolution as measured by MRI metrics at baseline and at months 1, 3, 8 and 9; 3) Changes from baseline to termination in EDSS; 4) The total number of confirmed relapses; and 5) Change from baseline to termination in Timed 25-Foot Walk test. MRI count data are analyzed using the over-dispersed Poisson regression as outlined for the primary end-point . .
- MRI volume changes from baseline to termination are analyzed using an analysis of covariance as described for the changes in the T2 lesions volume. Repeated measures analysis designed to elucidate the time course of the drug effect is also performed for all MRI parameters.
- the changes from baseline to termination in the EDSS and in the Timed 25-Foot Walk test are analyzed using an analysis of covariance as outlined for the change from baseline to termination in total volume of T2 lesions .
- Each patient is ' evaluated by an Examining Neurologist for the neurological exam and relapse evaluation.
- the Treating Neurologist sees the subject for relapse confirmation, based on the Examining Neurologists' findings, and may prescribe steroid treatment if warranted.
- the Examining Neurologist performs all neurological evaluations throughout the study.
- FS, EDSS score, and Timed 25-Foot Walk is assessed based on standardized neurological examination and slightly modified FS and EDSS (Neurostatus L. Kappos, Dept. of Neurology, University Hospital, CH-4031/Basel),.
- a relapse is defined as the appearance of one or more new neurological abnormalities or the reappearance of one or more previously observed neurological abnormalities .
- An event is counted as a relapse only when the subject's symptoms are accompanied by observed objective neurological changes, consistent with: a) an increase of at least 0.5 in the EDSS score or one grade in the score of two or more of the seven FS; or, b) two grades in the score of one of FS as compared to the previous evaluation.
- the subject must not be undergoing any acute metabolic changes such as fever or other medical abnormality.
- a change in bowel/bladder function or in cognitive function must, not be -entirely responsible-f-or--the changes in EDSS or FS scores.
- a complete neurological assessment is performed at screening, baseline, and month 9 (or early termination visit) .
- a complete neurological assessment is also performed during a schedule or unscheduled visit when the subject's complaint is suggestive of a relapse.
- the decision as to whether the neurological change is considered a confirmed relapse is made by the Treating Physician, based on EDSS/FS scores assessed by the Examining Physician. .
- Treating Neurologist evaluates the subject once any symptom suggestive of a relapse occurs . - In the presence of symptoms suggestive of a relapse during a scheduled or unscheduled visit, the Treating Neurologist will refer the patient to the Examining Neurologist.
- corticosteroids should be administered for the treatment of the relapse.
- a ' fixed dose of 1 g/day of I.V. methylprednisolone (Solumedrol ® ) for 3 consecutive days maximum is the treatment allowed in this protocol. No tapering off is allowed.
- Subjects are treated with a daily ,dose of 20 mg of GA in combination with a twice-daily dose of 100 g of minocycline or with a daily dose of 20 mg of GA in combination with a placebo.
- GA is supplied by Teva Pharmaceitical Industries Ltd, Israel.
- the minocycline and placebo are supplied by Novopharm Ltd, Canada .
- Patients treated with the COPAXONE® and minocycline combination exhibit a comparable or greater reduction in Tl and T2 Gd- enhancing lesions and other lesions, as compared to the group receiving COPAXONE® and placebo. Additionally, the group receiving the COPAXONE® and minocycline combination demonstrate a comparable or greater reduction in the number of relapses per year as compared with the group receiving COPAXONE® and placebo.
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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US11/597,571 US20070238711A1 (en) | 2004-05-28 | 2005-05-27 | Combination Therapy with Glatiramer Acetate and Minocycline for the Treatment of Multiple Sclerosis |
EP05754812A EP1758563A1 (en) | 2004-05-28 | 2005-05-27 | Combination therapy with glatiramer acetate and minocycline for the treatment of multiple sclerosis |
CA002569098A CA2569098A1 (en) | 2004-05-28 | 2005-05-27 | Combination therapy with glatiramer acetate and minocycline for the treatment of multiple sclerosis |
IL179330A IL179330A0 (en) | 2004-05-28 | 2006-11-16 | Combination therapy with glatiramer acetate and minocycline for the treatment of multiple sclerosis |
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US57511404P | 2004-05-28 | 2004-05-28 | |
US60/575,114 | 2004-05-28 |
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WO2005117902A1 true WO2005117902A1 (en) | 2005-12-15 |
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PCT/US2005/018938 WO2005117902A1 (en) | 2004-05-28 | 2005-05-27 | Combination therapy with glatiramer acetate and minocycline for the treatment of multiple sclerosis |
Country Status (5)
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US (1) | US20070238711A1 (en) |
EP (1) | EP1758563A1 (en) |
CA (1) | CA2569098A1 (en) |
IL (1) | IL179330A0 (en) |
WO (1) | WO2005117902A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2016020944A1 (en) * | 2014-08-04 | 2016-02-11 | Fabrizio De Silvestri | Use in single pill/tablet/capsule of minocycline, fluconazole and atorvastatin in the treatment of multiple sclerosis |
Families Citing this family (1)
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KR101455933B1 (en) * | 2013-05-28 | 2014-10-31 | 가톨릭대학교 산학협력단 | Effective combination of human bone marrow mesenchymal stem cells and minocycline in Multiple sclerosis |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6613456B2 (en) * | 1997-07-09 | 2003-09-02 | Nec Corporation | Organic electroluminescent device |
US20040013643A1 (en) * | 2000-09-19 | 2004-01-22 | Novlmmune S.A. | Methods for treatment of multiple sclerosis with statins |
Family Cites Families (4)
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AU2002360696A1 (en) * | 2001-12-21 | 2003-07-30 | Ilex Oncology, Inc. | Combination comprising anti-cd52 antibodies and other therapeutic agents for treatment for multiple sclerosis |
CA2518079A1 (en) * | 2003-03-04 | 2004-10-28 | Teva Pharmaceutical Industries, Ltd. | Combination therapy with glatiramer acetate and alphacalcidol for the treatment of multiple sclerosis |
PT1638589E (en) * | 2003-05-14 | 2014-06-12 | Teva Pharma | Combination therapy with glatiramer acetate and mitoxantrone for the treatment of multiple sclerosis |
CA2534711A1 (en) * | 2003-08-01 | 2005-02-10 | Medarex, Inc. | Combination therapies for multiple sclerosis |
-
2005
- 2005-05-27 EP EP05754812A patent/EP1758563A1/en not_active Withdrawn
- 2005-05-27 WO PCT/US2005/018938 patent/WO2005117902A1/en active Application Filing
- 2005-05-27 CA CA002569098A patent/CA2569098A1/en not_active Abandoned
- 2005-05-27 US US11/597,571 patent/US20070238711A1/en not_active Abandoned
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2006
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6613456B2 (en) * | 1997-07-09 | 2003-09-02 | Nec Corporation | Organic electroluminescent device |
US20040013643A1 (en) * | 2000-09-19 | 2004-01-22 | Novlmmune S.A. | Methods for treatment of multiple sclerosis with statins |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016020944A1 (en) * | 2014-08-04 | 2016-02-11 | Fabrizio De Silvestri | Use in single pill/tablet/capsule of minocycline, fluconazole and atorvastatin in the treatment of multiple sclerosis |
US10610592B2 (en) | 2014-08-04 | 2020-04-07 | Fabrizio De Silvestri | Treatment of multiple sclerosis |
Also Published As
Publication number | Publication date |
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CA2569098A1 (en) | 2005-12-15 |
IL179330A0 (en) | 2007-05-15 |
EP1758563A1 (en) | 2007-03-07 |
US20070238711A1 (en) | 2007-10-11 |
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