Bertrand L. Chenard - Waterford CT Frank S. Menniti - Mystic CT Mario D. Saltarelli - Mystic CT
Assignee:
Pfizer, Inc. - New York NY
International Classification:
A61K 3144
US Classification:
514304, 514319, 514320, 514327
Abstract:
This invention relates to methods of treating traumatic brain injury (TBI) or hypoxic or ischemic stroke, comprising administering to a patient in need of such treatment an NR2B subtype selective N-methyl-D-aspartate (NMDA) receptor antagonist in combination with either: (a) a sodium channel antagonist; (b) a nitric oxide synthase (NOS) inhibitor; (c) a glycine site antagonist; (d) a potassium channel opener; (e) an AMPA/kainate receptor antagonist; (f) a calcium channel antagonist; (g) a GABA-A receptor modulator (e. g. , a GABA-A receptor agonist); or (h) an antiinflammatory agent. This invention also relates to methods of treating hypoxic or ischemic stroke comprising administering to a patient in need of such treatment an NMDA receptor antagonist in combination with a thrombolytic agent.
Bertrand L. Chenard - Waterford CT, US Mario Saltarelli - Lake Bluff IL, US Frank S. Menniti - Mystic CT, US
Assignee:
Pfizer Inc - New York NY
International Classification:
A61K031/445
US Classification:
514327, 514315, 514323
Abstract:
The invention provides new methods for treating certain disorders resulting from neurodegeneration and for treating depression which comprise administration of NR2B subunit selective NMDA antagonists. The disorders that can be treating by the invention include hearing loss, vision loss, neurodegeneration caused by epileptic seizures, neurotoxin poisoning, Restless Leg Syndrome, multi-system atrophy, non-vascular headache, and depression.
Bertrand L. Chenard - Waterford CT, US Frank S. Menniti - Mystic CT, US Mario D. Saltarelli - Mystic CT, US
Assignee:
Pfizer Inc - New York NY
International Classification:
A61K 31/44
US Classification:
514299, 514315, 514317
Abstract:
The invention provides new methods for treating certain disorders resulting from neurodegeneration and for treating depression which comprise administration of NR2B subunit selective NMDA antagonists. The disorders that can be treating by the invention include hearing loss, vision loss, neurodegeneration caused by epileptic seizures, neurotoxin poisoning, Restless Leg Syndrome, multi-system atrophy, non-vascular headache, and depression.
Treatment Of Attention-Deficit/Hyperactivity Disorder
Earle E. Bain - Libertyville IL, US Walid M. Abi-Saab - Dornach, CH Sandeep Dutta - Gurnee IL, US Tushar S. Garimella - Skokie IL, US Walid M. Awni - Libertyville IL, US Mario D. Saltarelli - Lake Bluff IL, US
Assignee:
Abbott Laboratories - Abbott Park IL
International Classification:
A61K 31/44
US Classification:
514338
Abstract:
3-(5,6-Dichloro-pyridin-3-yl)-1S,5S-3,6-diazabicyclo[3. 2. 0]heptane and salts thereof are effective nicotinic receptor agonist compounds that demonstrated pharmacological effect for symptoms associated with attention-deficit/hyperactivity disorder.
Method Of Treating Acute, Chronic And/Or Neuropathic Pain
FRANK S. MENNITI - MYSTIC CT, US BERTRAND L. CHENARD - WATERFORD CT, US MARIO D. SALTARELLI - MYSTIC CT, US JONATHON M. PARKER - SALEM CT, US
International Classification:
A61K031/55 A61K031/44 A61K031/47 A61K031/445
US Classification:
514/278000, 514/327000, 514/216000, 514/315000
Abstract:
This invention relates to a method of treating acute, chronic and/or neuropathic pain in which a mammal suffering from acute, chronic and/or neuropathic pain is treated with an effective amount of an NR2B selective NMDA antagonist having a ratio of NR2B receptor activity to -adrenergic receptor activity of at least about 3:1.
Pharmaceutical Uses For Fluoroalkoxybenzylamino Derivatives Of Nitrogen Containing Heterocycles
Phillip Chappell - Guilford CT, US Brian O'Neill - Old Saybrook CT, US Mario Saltarelli - Mystic CT, US
International Classification:
A61K031/277 A61K031/135
US Classification:
514/524000, 514/649000
Abstract:
The present invention relates to methods of treating various CNS and other disorders by adminstering fluoroalkoxybenzylamino derivatives of nitrogen containing heterocyclic compounds, and specifically, by administering compounds of the formula wherein Q, X, Xand Xare as defined below, and their pharmaceutically acceptable salts.
Pharmaceutical Combinations For The Treatment Of Stroke And Traumatic Brain Injury
Bertrand Chenard - Waterford CT, US Frank Menniti - Mystic CT, US Mario Saltarelli - Mystic CT, US
International Classification:
A61K031/353 A61K031/075 A61K031/05
US Classification:
514/456000, 514/718000, 514/731000
Abstract:
This invention relates to methods of treating traumatic brain injury (TBI) or hypoxic or ischemic stroke, comprising administering to a patient in need of such treatment an NR2B subtype selective N-methyl-D-aspartate (NMDA) receptor antagonist in combination with either: (a) a neutrophil inhibitory factor (NIF); (b) a sodium channel antagonist; (c) a nitric oxide synthase (NOS) inhibitor; (d) a glycine site antagonist; (e) a potassium channel opener; (f) an AMPA/kainate receptor antagonist; (g) a calcium channel antagonist; (h) a GABA-A receptor modulator (e.g., a GABA-A receptor agonist); or (i) an antiinflammatory agent.
Prophylactic Use Of N-Methyl-D-Aspartate (Nmda) Antagonists
Bertrand Chenard - Waterford CT, US Mario Saltarelli - Mystic CT, US Erika Schneider - Westwood MA, US Mark Field - Great Dunmow, GB Frank Menniti - Mystic CT, US
International Classification:
A61K031/00
US Classification:
514/001000
Abstract:
This invention provides a method of inhibiting in a mammal neurological damage resulting from impairment of glucose and/or oxygen supply to the brain, which method comprises administering to the mammal prior to the impairment of glucose and/or oxygen supply to the brain an amount of an NR2B subunit selective NMDA antagonist, which amount is effective in inhibiting neurological damage. This invention also provides a method of preventing primary hyperalgesia, secondary hyperalgesia, primary allodynia, secondary allodynia, or other pain caused by central sensitization, in a mammal, which method comprises administering to the mammal, prior to affliction with said pain, an amount of an NR2B subunit selective NMDA antagonist, which amount is effective in preventing said pain.