Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:7623616rdf:typepubmed:Citationlld:pubmed
pubmed-article:7623616lifeskim:mentionsumls-concept:C0030705lld:lifeskim
pubmed-article:7623616lifeskim:mentionsumls-concept:C0002395lld:lifeskim
pubmed-article:7623616lifeskim:mentionsumls-concept:C0036043lld:lifeskim
pubmed-article:7623616lifeskim:mentionsumls-concept:C0288577lld:lifeskim
pubmed-article:7623616pubmed:issue5lld:pubmed
pubmed-article:7623616pubmed:dateCreated1995-8-28lld:pubmed
pubmed-article:7623616pubmed:abstractTextCI-979 ((E)-1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxaldehyde, O-methyloxime monohydrochloride), a novel muscarinic agonist, is being investigated as a potential treatment for Alzheimer's disease (AD). The objective of the present study was to determine the safety and tolerance of multiple, rising, oral doses of CI-979 in patients with AD. Ten male patients aged 59 to 74 years (mean 65 years) who met NINCDS criteria for AD were randomized to receive either CI-979 (eight patients) or placebo (two patients) according to a double-blind, parallel-group, rising-dose design. Doses were 0.5-mg q6h, 1-mg q12h, 1-mg q6h, 2-mg q12h, 2-mg q6h, 2.5-mg q6h, and 3-mg q6h. All doses were to be administered sequentially for 3 days each with the exception of the 2.5-mg q6h dose, which was to be administered for 1.5 days. Five patients receiving CI-979 discontinued study medication because of adverse events; two after receiving 2-mg q6h (10 doses), two after 2.5-mg q6h (5 doses), and one after 3-mg q6h (4 doses). The study was terminated following administration of the fourth 3-mg dose due to the nature and intensity of adverse events. Cholinergic symptoms including diaphoresis, hypersalivation, nausea, diarrhea, hypotension, chills, headache, flatulence, and urinary frequency and signs suggestive of parkinsonism (cogwheeling, tremor, pillrolling, posturing, and shuffling gait) were dose-limiting. The frequency and intensity of adverse events increased with increasing CI-979 dose. No other clinically significant CI-979-related changes occurred in physical examinations, clinical laboratory measurements, electrocardiograms, or ophthalmologic examinations. Steady-state trough plasma CI-979 concentrations increased in proportion to dose. In summary, CI-979 doses of 1-mg q6h were well tolerated by all patients; 2-mg q6h was tolerated by most patients, and 2.5-mg and 3-mg doses were poorly tolerated, Dose titration to a maximum of 2-mg q6h will therefore be used in initial efficacy trials of CI-979 in patients with AD.lld:pubmed
pubmed-article:7623616pubmed:languageenglld:pubmed
pubmed-article:7623616pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:7623616pubmed:citationSubsetIMlld:pubmed
pubmed-article:7623616pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:7623616pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:7623616pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:7623616pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:7623616pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:7623616pubmed:statusMEDLINElld:pubmed
pubmed-article:7623616pubmed:issn0024-3205lld:pubmed
pubmed-article:7623616pubmed:authorpubmed-author:CutlerN RNRlld:pubmed
pubmed-article:7623616pubmed:authorpubmed-author:ReeceP APAlld:pubmed
pubmed-article:7623616pubmed:authorpubmed-author:SedmanA JAJlld:pubmed
pubmed-article:7623616pubmed:authorpubmed-author:SramekJ JJJlld:pubmed
pubmed-article:7623616pubmed:authorpubmed-author:BockbraderHHlld:pubmed
pubmed-article:7623616pubmed:authorpubmed-author:HouraniJJlld:pubmed
pubmed-article:7623616pubmed:issnTypePrintlld:pubmed
pubmed-article:7623616pubmed:volume57lld:pubmed
pubmed-article:7623616pubmed:ownerNLMlld:pubmed
pubmed-article:7623616pubmed:authorsCompleteYlld:pubmed
pubmed-article:7623616pubmed:pagination503-10lld:pubmed
pubmed-article:7623616pubmed:dateRevised2004-11-17lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:meshHeadingpubmed-meshheading:7623616-...lld:pubmed
pubmed-article:7623616pubmed:year1995lld:pubmed
pubmed-article:7623616pubmed:articleTitleSafety and tolerability of CI-979 in patients with Alzheimer's disease.lld:pubmed
pubmed-article:7623616pubmed:affiliationCalifornia Clinical Trials, Beverly Hills 90211, USA.lld:pubmed
pubmed-article:7623616pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7623616pubmed:publicationTypeClinical Triallld:pubmed
pubmed-article:7623616pubmed:publicationTypeRandomized Controlled Triallld:pubmed