Milnacipran: Difference between revisions
→Fibromyalgia: Removed reference to two trials. Replaced with systematic review. |
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===Fibromyalgia=== |
===Fibromyalgia=== |
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During its development for fibromyalgia, milnacipran was evaluated utilizing a composite responder approach. To be considered as a responder for the composite ‘treatment of fibromyalgia’ endpoint, each patient had to show concurrent and clinically meaningful improvements in pain, physical function and global impression of disease status. |
During its development for fibromyalgia, milnacipran was evaluated utilizing a composite responder approach. To be considered as a responder for the composite ‘treatment of fibromyalgia’ endpoint, each patient had to show concurrent and clinically meaningful improvements in pain, physical function and global impression of disease status. A systematic review in 2012 showed moderate relief for a minority of people with fibromyalgia. Milnacipran was associated with increased adverse events and discontinuing use of the drug.<ref>{{cite journal|last=Derry|first=S|coauthors=Gill, D; Phillips, T; Moore, RA|title=Milnacipran for neuropathic pain and fibromyalgia in adults.|journal=Cochrane database of systematic reviews (Online)|date=2012 Mar 14|volume=3|pages=CD008244|pmid=22419330}}</ref> |
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|author=Clauw DJ, Mease P, Palmer RH, Gendreau RM, Wang Y |
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|title=Milnacipran for the treatment of fibromyalgia in adults: a 15-week, multicenter, randomized, double-blind, placebo-controlled, multiple-dose clinical trial |
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|journal=Clinical Therapeutics |
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|volume=30 |
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|issue=11 |
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|pages=1988–2004 |
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|year=2008 |
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|pmid=19108787 |
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|doi=10.1016/j.clinthera.2008.11.009 |
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}}</ref><ref name="mease">{{cite journal |
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|author=Mease PJ, Clauw DJ, Gendreau RM, Rao SG, Kranzler J, Chen W, Palmer RH |
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|title=The efficacy and safety of milnacipran for treatment of fibromyalgia. a randomized, double-blind, placebo-controlled trial |
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|journal=Journal Rheumatology |
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|volume=36 |
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|issue=2 |
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|pages=398–409 |
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|year=2009 |
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|pmid=19132781 |
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|doi=10.3899/jrheum.080734 |
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}}</ref> involving a total of over 2000 patients have shown milnacipran, at both 100 and 200 mg/day, to be significantly more effective than placebo in treating both pain and the broader syndrome of fibromyalgia. Response rates with milnacipran were similar in patients with and without co-morbid depression. |
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==Side effects== |
==Side effects== |
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The most frequently occurring adverse reactions (≥ 5% and greater than placebo) were nausea, headache, constipation, dizziness, insomnia, hot flush, hyperhidrosis, vomiting, palpitations, heart rate increase, dry mouth, and hypertension [FDA Savella prescribing information]. Milnacipran can have a significant impact on sexual functions, including both a decrease in sexual desire and ability. Milnacipran can cause pain and swelling of the testicles in men as well as blood in the urine and stools. The incidence of cardiovascular and [[anticholinergic]] side effects was significantly lower compared to [[Tricyclic antidepressant|TCA]]s as a controlled study with over 3,300 patients revealed. Elevation of [[liver enzymes]] without signs of symptomatic liver disease has been infrequent. Mood swing to [[mania]] has also been seen and dictates termination of treatment. In [[psychotic]] patients emergence of [[delirium]] has been noticed. Milnacipran has a low incidence of [[sedation]] but improves [[sleep]] (both duration and quality) in depressed patients. In [[Psychomotor agitation|agitated]] patients or those with [[suicidal]] thoughts additive sedative/anxiolytic treatment is usually indicated. |
The most frequently occurring adverse reactions (≥ 5% and greater than placebo) were nausea, headache, constipation, dizziness, insomnia, hot flush, hyperhidrosis, vomiting, palpitations, heart rate increase, dry mouth, and hypertension [FDA Savella prescribing information]. Milnacipran can have a significant impact on sexual functions, including both a decrease in sexual desire and ability. Milnacipran can cause pain and swelling of the testicles in men as well as blood in the urine and stools. The incidence of cardiovascular and [[anticholinergic]] side effects was significantly lower compared to [[Tricyclic antidepressant|TCA]]s as a controlled study with over 3,300 patients revealed. Elevation of [[liver enzymes]] without signs of symptomatic liver disease has been infrequent. Mood swing to [[mania]] has also been seen and dictates termination of treatment. In [[psychotic]] patients emergence of [[delirium]] has been noticed. Milnacipran has a low incidence of [[sedation]] but improves [[sleep]] (both duration and quality) in depressed patients. In [[Psychomotor agitation|agitated]] patients or those with [[suicidal]] thoughts additive sedative/anxiolytic treatment is usually indicated. |
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Revision as of 17:13, 30 May 2013
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| Clinical data | |
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| AHFS/Drugs.com | Consumer Drug Information |
| MedlinePlus | a609016 |
| Routes of administration | Oral |
| ATC code | |
| Legal status | |
| Legal status |
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| Pharmacokinetic data | |
| Bioavailability | 85% |
| Protein binding | 13% |
| Metabolism | Hepatic |
| Elimination half-life | 8 hours |
| Excretion | Renal |
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C15H22N2O |
| Molar mass | 246.348 g/mol g·mol−1 |
| 3D model (JSmol) | |
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| (verify) | |
Milnacipran (Ixel, Savella, Dalcipran, Toledomin) is a serotonin–norepinephrine reuptake inhibitor (SNRI) used in the clinical treatment of fibromyalgia. It is not approved for the clinical treatment of major depressive disorder in the USA, but it is in other countries.
Medical uses
Depression
In a pooled analysis of 7 comparative trials with imipramine,[1] milnacipran and imipramine were shown to have comparable efficacy while milnacipran was significantly better tolerated. A pooled analysis of studies comparing milnacipran and SSRIs [2] concluded a superior efficacy for milnacipran with similar tolerability for milnacipran and SSRIs. A more recent meta-analysis of 6 studies involving more than 1,000 patients showed no distinction between milnacipran and SSRIs in efficacy or discontinuation rates, including discontinuation for side effects or lack of efficacy.[3] A meta-analysis of a total of 16 randomized controlled trials with more than 2200 patients [4] concluded that there were no statistically significant differences in efficacy, acceptability and tolerability when comparing milnacipran with other antidepressant agents. However, compared with TCAs, significantly fewer patients taking milnacipran dropped out due to adverse events. As with other antidepressants, 1 to 3 weeks may elapse before significant antidepressant action becomes clinically evident.
Fibromyalgia
During its development for fibromyalgia, milnacipran was evaluated utilizing a composite responder approach. To be considered as a responder for the composite ‘treatment of fibromyalgia’ endpoint, each patient had to show concurrent and clinically meaningful improvements in pain, physical function and global impression of disease status. A systematic review in 2012 showed moderate relief for a minority of people with fibromyalgia. Milnacipran was associated with increased adverse events and discontinuing use of the drug.[5]
Side effects
The most frequently occurring adverse reactions (≥ 5% and greater than placebo) were nausea, headache, constipation, dizziness, insomnia, hot flush, hyperhidrosis, vomiting, palpitations, heart rate increase, dry mouth, and hypertension [FDA Savella prescribing information]. Milnacipran can have a significant impact on sexual functions, including both a decrease in sexual desire and ability. Milnacipran can cause pain and swelling of the testicles in men as well as blood in the urine and stools. The incidence of cardiovascular and anticholinergic side effects was significantly lower compared to TCAs as a controlled study with over 3,300 patients revealed. Elevation of liver enzymes without signs of symptomatic liver disease has been infrequent. Mood swing to mania has also been seen and dictates termination of treatment. In psychotic patients emergence of delirium has been noticed. Milnacipran has a low incidence of sedation but improves sleep (both duration and quality) in depressed patients. In agitated patients or those with suicidal thoughts additive sedative/anxiolytic treatment is usually indicated.
Interactions
- MAOIs - hyperserotonergia (serotonin syndrome), potentially lethal hypertensive crisis
- 5-HT1 receptor agonists - coronary vasoconstriction with risk of angina pectoris and myocardial infarction
- Epinephrine, Norepinephrine (also in local anesthesia) - hypertensive crisis and/or possible cardiac arrhythmia
- Clonidine - antihypertensive action of clonidine may be antagonized
- Digitalis - hemodynamic actions increased
- Alcohol - no interactions known; however, because milnacipran can cause mild elevation of liver enzymes, caution is recommended; the FDA advises against the concomitant use of alcohol and milnacipran
Contraindications
Administration of milnacipran should be avoided in individuals with the following:
- Known hypersensitivity to milnacipran (absolute contraindication)
- Patients under 15 years of age (no sufficient clinical data)
- Concomitant treatment with irreversible MAO inhibitors (e.g. tranylcypromine (Parnate), phenelzine (Nardil), >10 mg L-deprenyl (Selegiline)), digitalis glycosides or 5-HT1D-agonists (e.g. triptan migraine drugs) is an absolute contraindication.
Administration of milnacipran should be done with caution in individuals with the following:
- Concomitant treatment with parenteral epinephrine, norepinephrine, with clonidine and reversible MAO-A Inhibitors (moclobemide, toloxatone).
- Advanced renal disease (decreased dosage required)
- Hypertrophy of the prostate gland (possibly urination hesitancy induced), with hypertension and heart disease (tachycardia may be a problem) as well as with open angle glaucoma
Milnacipran should not be used during pregnancy because it may cross the placenta barrier and no clinical data exists on harmful effects in humans and animal studies. Milnacipran is contraindicated during lactation because it is excreted in the milk, and it is not known if it is harmful to the newborn.
Pharmacology
Milnacipran inhibits the reuptake of serotonin and norepinephrine in an approximately 1:3 ratio, respectively; in practical use this means a relatively balanced action upon both neurotransmitters. Increasing both neurotransmitters concentration simultaneously works synergistically to treat both depression and fibromyalgia. Milnacipran exerts no significant actions on H1, α1, D1, D2, and mACh receptors, as well as on benzodiazepine and opioid binding sites.[6][7][8]
Pharmacokinetics
Milnacipran is well absorbed after oral dosing and has a bioavailability of 85%. Meals do not have an influence on the rapidity and extent of absorption. Peak plasma concentrations are reached 2 hours after oral dosing. The elimination half-life of 8 hours is not increased by liver impairment and old age, but by significant renal disease. Milnacipran is conjugated to the inactive glucuronide and excreted in the urine as unchanged drug and conjugate. Only traces of active metabolites are found.
Regulatory status
Milnacipran is indicated for:
- treatment of major depressive disorder (not in USA)
- management of fibromyalgia (USA and Russia)
The recommended dose for depression is 100 mg/day (given as 50 mg 2 times daily), with a starting period of 4 days on 25 mg/day. The dose should be decreased in patients with renal disease. The recommended dose for fibromyalgia is 100 mg/day (after an uptitration period ) which may be increased to 200 mg/day based on individual patient response.
After successful treatment of the acute depressive episode, patients should be maintained on milnacipran for several months (normally 9 months) in order to prevent relapse of depression.
In America, Savella® is supplied by Forest Pharmaceuticals in a 2-week, professional sample titration pack to be provided directly by the doctor to the patient initiating milnacipran therapy. This pack contains five 12.5 mg tablets (one on day one, one tablet twice a day on days 2-3), eight 25 mg tablets (one tablet twice a day on days 4-7), and fourteen 50 mg tablets (one tablet twice a day on days 8-14). Therapy is then continued with one 50 mg tablet twice a day, or adjusted as needed by the physician.
History
Milnacipran was first approved for the treatment of major depressive episodes in France in December 1996. It is currently marketed (as Ixel) for this indication in over 45 countries worldwide including several European countries such as Austria, Bulgaria, Finland, France, Portugal, and Russia. It is also available in Japan (as Toledomin) and Mexico (as Dalcipran). Cypress Bioscience bought the exclusive rights for approval and marketing of the drug for any purpose in the United States and Canada in 2003 from the manufacturer Laboratoires Pierre Fabre.
In January 2009 the U.S. Food and Drug Administration (FDA) approved milnacipran (under the brand name Savella) only for the treatment of fibromyalgia, making it the third medication approved for this purpose in the United States. In July and November 2009, the European Medicines Agency refused marketing authorization for a milnacipran product (under the brand name Impulsor) for the treatment of fibromylagia.[9]
References
- ^ Kasper S, Pletan Y, Solles A, Tournoux A (1996). "Comparative studies with milnacipran and tricyclic antidepressants in the treatment of patients with major depression: a summary of clinical trial results". International Clinical Psychopharmacolgy. 11 (Suppl 4): 35–39. doi:10.1097/00004850-199609004-00005. PMID 8923125.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Lopez-Ibor J, Guelfi JD, Pletan Y, Tournoux A, Prost JF (1996). "Milnacipran and selective serotonin reuptake inhibitors in major depression". International Clinical Psychopharmacology. 11 (Suppl 4): 41–46. doi:10.1097/00004850-199609004-00006. PMID 8923126.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Papakostas GI, Fava M (2007). "A meta-analysis of clinical trials comparing milnacipran, a serotonin--norepinephrine reuptake inhibitor, with a selective serotonin reuptake inhibitor for the treatment of major depressive disorder". European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. 17 (1): 32–6. doi:10.1016/j.euroneuro.2006.05.001. PMID 16762534.
- ^ Nakagawa A, Watanabe N, Omori IM, Barbui C, Cipriani A, McGuire H, Churchill R, Furukawa TA (2009). Nakagawa, Atsuo (ed.). "Milnacipran versus other antidepressive agents for depression". Cochrane Database of Systematic Reviews. 8 (3): CD006529. doi:10.1002/14651858.CD006529.pub2. PMID 19588396.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Derry, S (2012 Mar 14). "Milnacipran for neuropathic pain and fibromyalgia in adults". Cochrane database of systematic reviews (Online). 3: CD008244. PMID 22419330.
{{cite journal}}: Check date values in:|date=(help); Unknown parameter|coauthors=ignored (|author=suggested) (help) - ^ Moret C, Charveron M, Finberg JP, Couzinier JP, Briley M (1985). "Biochemical profile of midalcipran (F 2207), 1-phenyl-1-diethyl-aminocarbonyl-2-aminomethyl-cyclopropane (Z) hydrochloride, a potential fourth generation antidepressant drug". Neuropharmacology. 24 (12): 1211–9. doi:10.1016/0028-3908(85)90157-1. PMID 3005901.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Briley M, Prost JF, Moret C (1996). "Preclinical pharmacology of milnacipran". International clinical psychopharmacology. 11 Suppl 4: 9–14. PMID 8923122.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Puozzo C, Panconi E, Deprez D (2002). "Pharmacology and pharmacokinetics of milnacipran". International clinical psychopharmacology. 17 Suppl 1: S25–35. PMID 12369608.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ European Medicines Agency. "Questions and answers on the recommendati on for the refusal of the marketing authorisation for Milnacipran Pierre Fabre Médicament/Impulsor" (PDF). European Medicines Agency. Retrieved 30 May 2013.