Synonyms: Exelon™, Rivastigmine tartrate , Rivastach® Patch, Prometax®, SDZ ENA 713
Chemical Name: (S)-3-[1-(dimethylamino)ethyl]phenyl N-ethyl-N-methylcarbamate
Therapy Type: Small Molecule
Target Type: Cholinergic System
Condition(s): Alzheimer's Disease, Parkinson's Disease Dementia
U.S. FDA Status: Alzheimer's Disease (Approved), Parkinson's Disease Dementia (Approved)
Company: Novartis Pharmaceuticals Corporation
Approved for: Mild to moderate Alzheimer’s disease and mild to moderate dementia related to Parkinson's disease
Rivastigmine is a reversible inhibitor of both the acetylcholinesterase and butyrylcholinesterase enzymes. It is widely used for the treatment of Alzheimer's across its mild, moderate, and severe stages, as well as for the treatment of dementia associated with Parkinson's disease (PDD). Rivastigmine was first approved to be marketed for AD in 1997 in Switzerland, and in the years since has come to be available in some 80 countries worldwide, including the United States, Canada, and Europe, for both AD and PDD.
This drug was originally formulated as a twice-daily oral capsule, and it was the first AD therapy to be made available as a skin patch that provides continuous delivery of the drug over 24 hours. The patch is sold in three doses, though not all are available in all countries. By way of transdermal absorption, the patch provides steady plasma concentrations of rivastigmine and bypasses first-pass metabolism in the intestine and liver. Because it generates markedly fewer gastrointestinal side effects, it enables patients to receive a higher therapeutic dose (Cummings et al., 2007). Generic versions of different doses of rivastigmine capsules started becoming available in 2010. A generic version of the rivastigmine transdermal patch is on hold pending resolution of a patent dispute (Law360 story).
Rivastigmine's side effects are consistent with class effects of cholinesterase inhibition. They include most commonly nausea, vomiting, diarrhea, and loss of appetite, and less frequently agitation, depression, dizziness, fatigue/sleeplessness, and others. Side effects tend to be strongest in the beginning weeks, when the dose is titrated up to the therapeutic level, and milder in the maintenance phase. Apart from rare skin sensitivity reactions, the patch is generally better tolerated than the capsules.
About 65 clinical trials Phase 2 and higher have been registered with rivastigmine. For example, in a six-month North American trial comparing a dose of 6-12 mg/day to 1-4 mg/day and to placebo in 699 patients with mild to moderate AD, rivastigmine capsules showed a modest but dose-dependent treatment benefit on cognition, function, and activities of daily living as measured by the ADAS-cog, the CIBIC-plus, and the Progressive Deterioration Scale (PDS), respectively. A similar European trial in 725 patients with mild to moderate AD that compared 6-12 mg/day to 1-4 mg/day of rivastigmine and placebo, also for six months and using the same outcome measures, had similar results. Only a quarter to a third of patients had a significant treatment response to rivastigmine capsules (Corey-Bloom et al., 1998; Rosler et al., 1999).
The skin patch formulation was evaluated in the six-month, Phase 3 IDEAL (Investigation of transDermal Exelon in ALzheimer's disease) study in 1,195 patients with mild to moderate AD. Participants received either one of two doses of the rivastigmine patch (9.5 or 17.4 mg over the course of 24 hours), 6-mg twice-daily capsules, or placebo. On efficacy, both doses of the patch outperformed placebo; the lower-dose patch with a similar effect to that of the capsules, the high-dose patch adding a small benefit on cognition. With the patch, the incidence of gastrointestinal complaints dropped nearly to that of placebo, and two-thirds of caregivers said they preferred the patch. More recently, a six-month, 716-patient trial comparing a 4.6 mg/24-hour to a 13.3 mg/24-hour patch reported that the higher dose was more efficacious at comparable tolerability (e.g., Grossberg et al., 2007; Grossberg et al., 2011; Farlow et al., 2013). An open-label study in a real-life clinical setting outside of randomized controlled trials reported that 969 patients with mild to moderate AD treated with the rivastigmine patch tended to maintain cognitive and global function over 18 months (Gauthier et al., 2013).
Most double-blind randomized controlled trials of rivastigmine lasted three to six months; however, some longer-term treatment data are available from open-label extensions or from analyses of clinical observation. For example, one study of 1,998 patients treated for up to five years found that their mean baseline MMSE score of 19.3 declined to above 10 points after five years of rivastigmine treatment, while model-based projections predicted that without treatment it would have declined to below 10 points by three years. Other studies reported clinically meaningful treatment benefits compared with historical controls for two years of treatment (Small et al., 2005; Grossberg et al., 2004).
Overall, the acetylcholinesterase therapies donepezil, rivastigmine, and galantamine are viewed as having similar efficacy and safety, but direct side-by-side comparisons are few. One three-month study randomized 111 patients with mild to moderate AD to either donepezil titrated up to 10 mg once daily, or rivastigmine capsules up to 6 mg twice daily. Both regimens led to comparable symptomatic benefits on cognition. Donepezil was better tolerated, though this has since changed with the rivastigmine patch (Wilkinson et al., 2001). A two-year trial comparing rivastigmine to donepezil in 994 patients with moderate to severe AD found that almost half dropped out, most due to gastrointestinal side effects. Patients who continued had a similar benefit with either therapy on measures of cognition and behavior, though rivastigmine appeared to perform slightly better on activities of daily living and global function. Subgroup analyses hinted at better results for rivastigmine in patients with a particular butyrylcholinesterase genotype and patients who had symptoms of concomitant Lewy body disease, as well (Bullock et al, 2005).
Several trials have evaluated rivastigmine for dementia with Lewy bodies and Parkinson's disease dementia. This came up when routine clinical use of cholinesterase inhibitors in dementia patients with symptoms other than typical AD seemed to show a cognitive and clinical benefit in a large minority of such patients (Pakrasi et al., 2003). One multicenter, five-month trial in 120 patients with DLB showed a benefit on apathy, anxiety, delusions, hallucinations, as well as on cognitive performance and attention in the treatment group. About two-thirds of the treated patients had a clinically signifcant response to rivastigmine (McKeith et al., 2000). Hallucinations are a hallmark symptom of DLB and PDD and represent an area of overlap between these forms of dementia and AD; retrospective analysis of several trials indicates that AD patients with hallucinations respond better to rivastigmine treatment than those without (Cummings et al., 2010). More broadly, rivastigmine treatment appears to reduce somewhat the concomitant use of antipsychotic medications in people with AD (Scharre et al., 2010). How to manage behavioral symptoms of AD has become a pressing issue since 2005, when the FDA responded with a black-box warning to reports of increased mortality in dementia patients on antipsychotics (see Feb 2011 news story; Oct 2005 news story).
The EXPRESS (EXelon in PaRkinson's disEaSe dementia Study) trial tested 3 to 12 mg/day of rivastigmine capsules in 541 patients with Parkinson's disease dementia, first for six months in a double-blind and placebo controlled phase, and then in an open-label extension. At six months, treated patients improved modestly on cognition, overall function, and psychiatric symptoms. By 48 weeks, the mean ADAS-cog score for the treatment group remained above baseline, and placebo patients who switched to rivastigmine for the extension phase had a treatment benefit similar to that of the original rivastigmine group during the double-blind trial. Again, patients with hallucinations tended to respond better (e.g., Poewe et al., 2006). Rivastigmine also appeared to improve apathy in patients with advanced PD who did not yet have dementia; this finding is from a small trial conducted in France (Devos et al., 2013).
More recently, Novartis ran an 18-month trial comparing the capsule and patch formulations in 583 patients with mild to moderately severe PDD. This trial specifically assessed whether long-term treatment with rivastigmine improves cognitive and psychiatric symptoms of PDD at the cost of worsening motor symptoms. Data from NCT00623103 are not published yet. Traditionally, cholinergic agents have been considered counterindicated for the motor and autonomic aspects of PD. This is in part because anticholinergic drugs have been used for the symptomatic treatment of PD since the late 19th century, particularly muscarinic receptor antagonists. This view is changing. Guidelines by the U.K. National Institute for Health and Clinical Excellence (NICE) challenge the evidence for the safety and effectiveness of anticholinergics in PD and recommend against their use as a first-line treatment in this disease, particularly in patients with cognitive dysfunction (see guideline).
Some studies indicate that rivastigmine may have an effect on cerebrovascular factors influencing dementia. Alzheimer's patients who also have cardiovascular risk factors such as hypertension have been reported to respond better to rivastigmine than patients with more "pure" Alzheimer's disease, and some evidence exists for a treatment benefit of rivastigmine for vascular dementia (e.g., Erkinjuntti et al., 2003; Farlow et al., 2011; Birks et al., 2013).
For some years after cholinesterase inhibitor therapies were initially approved for Alzheimer's disease, their modest effect size created controversy about their cost-effectiveness (see Jul 2004 news story and extensive commentary). Since then, studies have shown that rivastigmine is modestly effective in the long-term treatment of AD, see above. Pharmacoeconomic studies in the United States and European countries have generally found that cholinesterase inhibitor treatment reduces the cost of care (e.g., Nagy et al., 2011). In the United Kingdom, where this debate had called into question coverage of rivastigmine by its universal health care system, NICE in 2011 issued a guidance recommending the use of rivastigmine in the treatment of mild to moderate AD (see, e.g., Fillit et al., 1999; Wimo et al., 2003; NICE guidance).
Rivastigmine is being evaluated in trials of Down's syndrome, mild cognitive impairment in Parkinson's disease, supranuclear palsy, delirium, traumatic brain injury, and cocaine dependence. For a list of rivastigmine trials, see clinicaltrials.gov.
- Warning on Antipsychotics Heeded, But What’s the Alternative?
- More Trouble for Atypical Antipsychotics—Dementia Patients at Risk
- Cholinesterase Inhibitors Not What They're Cracked Up To Be?
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