JPS584718A - 新規適応症に用うる医薬製剤 - Google Patents
新規適応症に用うる医薬製剤Info
- Publication number
- JPS584718A JPS584718A JP10166581A JP10166581A JPS584718A JP S584718 A JPS584718 A JP S584718A JP 10166581 A JP10166581 A JP 10166581A JP 10166581 A JP10166581 A JP 10166581A JP S584718 A JPS584718 A JP S584718A
- Authority
- JP
- Japan
- Prior art keywords
- improvement
- aminoadamantane
- hydrochloride
- pharmaceutical
- sequelae
- 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.)
- Granted
Links
- 150000003839 salts Chemical class 0.000 claims abstract description 11
- DKNWSYNQZKUICI-UHFFFAOYSA-N amantadine Chemical compound C1C(C2)CC3CC2CC1(N)C3 DKNWSYNQZKUICI-UHFFFAOYSA-N 0.000 claims abstract description 10
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 18
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- 208000026106 cerebrovascular disease Diseases 0.000 claims description 8
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- 208000016285 Movement disease Diseases 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- WOLHOYHSEKDWQH-UHFFFAOYSA-N amantadine hydrochloride Chemical compound [Cl-].C1C(C2)CC3CC2CC1([NH3+])C3 WOLHOYHSEKDWQH-UHFFFAOYSA-N 0.000 abstract description 46
- 239000007901 soft capsule Substances 0.000 abstract description 6
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- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 4
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- 229930195729 fatty acid Natural products 0.000 abstract description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 3
- 208000032851 Subarachnoid Hemorrhage Diseases 0.000 abstract description 3
- 238000002844 melting Methods 0.000 abstract description 3
- 230000008018 melting Effects 0.000 abstract description 3
- 239000000829 suppository Substances 0.000 abstract description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract description 2
- 239000002671 adjuvant Substances 0.000 abstract description 2
- 239000004503 fine granule Substances 0.000 abstract description 2
- 239000000470 constituent Substances 0.000 abstract 4
- 229910002651 NO3 Inorganic materials 0.000 abstract 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 1
- 230000002490 cerebral effect Effects 0.000 abstract 1
- 229960001280 amantadine hydrochloride Drugs 0.000 description 37
- 230000000694 effects Effects 0.000 description 22
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- 229940079593 drug Drugs 0.000 description 19
- 201000010099 disease Diseases 0.000 description 16
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- 238000000034 method Methods 0.000 description 8
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- 238000010255 intramuscular injection Methods 0.000 description 7
- 238000010253 intravenous injection Methods 0.000 description 7
- 206010065559 Cerebral arteriosclerosis Diseases 0.000 description 6
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- 230000000607 poisoning effect Effects 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 230000003542 behavioural effect Effects 0.000 description 4
- 229910002090 carbon oxide Inorganic materials 0.000 description 4
- 230000002596 correlated effect Effects 0.000 description 4
- 201000000980 schizophrenia Diseases 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 206010010071 Coma Diseases 0.000 description 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Chemical compound OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
- 230000009471 action Effects 0.000 description 3
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- 208000015122 neurodegenerative disease Diseases 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 230000000750 progressive effect Effects 0.000 description 3
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- -1 Glycerin Fatty Acid Ester Chemical class 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 206010020772 Hypertension Diseases 0.000 description 2
- 206010024264 Lethargy Diseases 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
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- 230000007423 decrease Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000014509 gene expression Effects 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 210000003128 head Anatomy 0.000 description 2
- 230000035876 healing Effects 0.000 description 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 2
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 2
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 2
- 210000000936 intestine Anatomy 0.000 description 2
- 238000012417 linear regression Methods 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 235000012054 meals Nutrition 0.000 description 2
- 230000003340 mental effect Effects 0.000 description 2
- 230000027939 micturition Effects 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 208000010125 myocardial infarction Diseases 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 2
- 229940057838 polyethylene glycol 4000 Drugs 0.000 description 2
- 210000000664 rectum Anatomy 0.000 description 2
- 230000033764 rhythmic process Effects 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229940124597 therapeutic agent Drugs 0.000 description 2
- 206010001605 Alcohol poisoning Diseases 0.000 description 1
- 206010053942 Cerebral haematoma Diseases 0.000 description 1
- 206010010075 Coma hepatic Diseases 0.000 description 1
- 208000022540 Consciousness disease Diseases 0.000 description 1
- 208000028399 Critical Illness Diseases 0.000 description 1
- 206010011703 Cyanosis Diseases 0.000 description 1
- 206010012335 Dependence Diseases 0.000 description 1
- 208000002230 Diabetic coma Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 208000010201 Exanthema Diseases 0.000 description 1
- 206010015769 Extradural haematoma Diseases 0.000 description 1
- 206010018852 Haematoma Diseases 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 206010021639 Incontinence Diseases 0.000 description 1
- 206010021703 Indifference Diseases 0.000 description 1
- 201000009906 Meningitis Diseases 0.000 description 1
- 206010028813 Nausea Diseases 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 206010073261 Ovarian theca cell tumour Diseases 0.000 description 1
- 206010033799 Paralysis Diseases 0.000 description 1
- 206010034010 Parkinsonism Diseases 0.000 description 1
- BYPFEZZEUUWMEJ-UHFFFAOYSA-N Pentoxifylline Chemical compound O=C1N(CCCCC(=O)C)C(=O)N(C)C2=C1N(C)C=N2 BYPFEZZEUUWMEJ-UHFFFAOYSA-N 0.000 description 1
- 208000002151 Pleural effusion Diseases 0.000 description 1
- 206010036631 Presenile dementia Diseases 0.000 description 1
- 208000001431 Psychomotor Agitation Diseases 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 206010038743 Restlessness Diseases 0.000 description 1
- 208000008765 Sciatica Diseases 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229960003805 amantadine Drugs 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000002583 angiography Methods 0.000 description 1
- 239000003443 antiviral agent Substances 0.000 description 1
- 230000036528 appetite Effects 0.000 description 1
- 235000019789 appetite Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 210000001142 back Anatomy 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 210000004958 brain cell Anatomy 0.000 description 1
- 230000002612 cardiopulmonary effect Effects 0.000 description 1
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- 206010008118 cerebral infarction Diseases 0.000 description 1
- 210000004720 cerebrum Anatomy 0.000 description 1
- DERZBLKQOCDDDZ-JLHYYAGUSA-N cinnarizine Chemical compound C1CN(C(C=2C=CC=CC=2)C=2C=CC=CC=2)CCN1C\C=C\C1=CC=CC=C1 DERZBLKQOCDDDZ-JLHYYAGUSA-N 0.000 description 1
- 238000009535 clinical urine test Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
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- 230000000994 depressogenic effect Effects 0.000 description 1
- 235000018823 dietary intake Nutrition 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 206010013663 drug dependence Diseases 0.000 description 1
- 230000008451 emotion Effects 0.000 description 1
- 201000005884 exanthem Diseases 0.000 description 1
- 208000011318 facial edema Diseases 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
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- 206010016256 fatigue Diseases 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
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- 231100000869 headache Toxicity 0.000 description 1
- 201000001059 hepatic coma Diseases 0.000 description 1
- 208000007386 hepatic encephalopathy Diseases 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- XZZXIYZZBJDEEP-UHFFFAOYSA-N imipramine hydrochloride Chemical compound [Cl-].C1CC2=CC=CC=C2N(CCC[NH+](C)C)C2=CC=CC=C21 XZZXIYZZBJDEEP-UHFFFAOYSA-N 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 208000037797 influenza A Diseases 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 238000007449 liver function test Methods 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 230000006996 mental state Effects 0.000 description 1
- 210000001259 mesencephalon Anatomy 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
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- 238000012986 modification Methods 0.000 description 1
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- 208000031225 myocardial ischemia Diseases 0.000 description 1
- 230000008693 nausea Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
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- 238000012360 testing method Methods 0.000 description 1
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- 230000001225 therapeutic effect Effects 0.000 description 1
- 229940041597 tofranil Drugs 0.000 description 1
- 208000009999 tuberous sclerosis Diseases 0.000 description 1
- 208000019206 urinary tract infection Diseases 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
Landscapes
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10166581A JPS584718A (ja) | 1981-06-30 | 1981-06-30 | 新規適応症に用うる医薬製剤 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10166581A JPS584718A (ja) | 1981-06-30 | 1981-06-30 | 新規適応症に用うる医薬製剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS584718A true JPS584718A (ja) | 1983-01-11 |
| JPH022861B2 JPH022861B2 (enExample) | 1990-01-19 |
Family
ID=14306662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10166581A Granted JPS584718A (ja) | 1981-06-30 | 1981-06-30 | 新規適応症に用うる医薬製剤 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS584718A (enExample) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002045710A1 (en) * | 2000-12-07 | 2002-06-13 | Neuromolecular Inc. | Methods for treating neuropsychiatric disorders with nmda receptor antagonists |
| US7326730B2 (en) | 2000-02-22 | 2008-02-05 | Adamas Pharmaceuticals, Inc. | Aminoadamantane derivatives as therapeutic agents |
| US8058291B2 (en) | 2005-04-06 | 2011-11-15 | Adamas Pharmaceuticals, Inc. | Methods and compositions for the treatment of CNS-related conditions |
| US8168209B2 (en) | 2004-11-23 | 2012-05-01 | Adamas Pharmaceuticals, Inc. | Method and composition for administering an NMDA receptor antagonist to a subject |
| US9867793B2 (en) | 2009-12-02 | 2018-01-16 | Adamas Pharma, Llc | Method of administering amantadine prior to a sleep period |
| US10154971B2 (en) | 2013-06-17 | 2018-12-18 | Adamas Pharma, Llc | Methods of administering amantadine |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5250097B2 (ja) | 2011-12-12 | 2013-07-31 | 信越石英株式会社 | 単結晶シリコン引き上げ用シリカ容器及びその製造方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54143526A (en) * | 1978-02-22 | 1979-11-08 | Du Pont | Antiidepressant agent composition |
-
1981
- 1981-06-30 JP JP10166581A patent/JPS584718A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54143526A (en) * | 1978-02-22 | 1979-11-08 | Du Pont | Antiidepressant agent composition |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7326730B2 (en) | 2000-02-22 | 2008-02-05 | Adamas Pharmaceuticals, Inc. | Aminoadamantane derivatives as therapeutic agents |
| WO2002045710A1 (en) * | 2000-12-07 | 2002-06-13 | Neuromolecular Inc. | Methods for treating neuropsychiatric disorders with nmda receptor antagonists |
| US8168209B2 (en) | 2004-11-23 | 2012-05-01 | Adamas Pharmaceuticals, Inc. | Method and composition for administering an NMDA receptor antagonist to a subject |
| US8173708B2 (en) | 2004-11-23 | 2012-05-08 | Adamas Pharmaceuticals, Inc. | Method and composition for administering an NMDA receptor antagonist to a subject |
| US8058291B2 (en) | 2005-04-06 | 2011-11-15 | Adamas Pharmaceuticals, Inc. | Methods and compositions for the treatment of CNS-related conditions |
| US9867792B2 (en) | 2009-12-02 | 2018-01-16 | Adamas Pharma, Llc | Method of administering amantadine prior to a sleep period |
| US9867793B2 (en) | 2009-12-02 | 2018-01-16 | Adamas Pharma, Llc | Method of administering amantadine prior to a sleep period |
| US9867791B2 (en) | 2009-12-02 | 2018-01-16 | Adamas Pharma, Llc | Method of administering amantadine prior to a sleep period |
| US9877933B2 (en) | 2009-12-02 | 2018-01-30 | Adamas Pharma, Llc | Method of administering amantadine prior to a sleep period |
| US11197835B2 (en) | 2009-12-02 | 2021-12-14 | Adamas Pharma, Llc | Method of administering amantadine prior to a sleep period |
| US10154971B2 (en) | 2013-06-17 | 2018-12-18 | Adamas Pharma, Llc | Methods of administering amantadine |
| US10646456B2 (en) | 2013-06-17 | 2020-05-12 | Adamas Pharma, Llc | Methods of administering amantadine |
| US11903908B2 (en) | 2013-06-17 | 2024-02-20 | Adamas Pharma, Llc | Methods of administering amantadine |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH022861B2 (enExample) | 1990-01-19 |
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