Levosimendan

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Levosimendan
Levosimendan.svg
Levosimendan ball-and-stick.png
Systematic (IUPAC) name
2-[[4-[(4R)-4-methyl-6-oxo-4,5-dihydro-1H-pyridazin-3-yl]phenyl]hydrazinylidene]propanedinitrile
Clinical data
Trade names Simdax
AHFS/Drugs.com International Drug Names
Routes of
administration
IV
Legal status
Legal status
  • ℞ (Prescription only)
Pharmacokinetic data
Bioavailability 85% (oral)
Protein binding 97–98%
Metabolism Extensive hepatic
Biological half-life ~1 hour (levosimendan), 75–80 hours (metabolites)
Excretion urine (54%), feces (44%)
Identifiers
CAS Number 141505-33-1 YesY
ATC code C01CX08 (WHO)
PubChem CID 3033825
DrugBank DB00922 YesY
ChemSpider 2298414 YesY
UNII C6T4514L4E YesY
KEGG D04720 YesY
ChEBI CHEBI:50567 YesY
ChEMBL CHEMBL313136 N
Chemical data
Formula C14H12N6O
Molar mass 280.28 g/mol
 NYesY (what is this?)  (verify)

Levosimendan (INN) /ˌlvsˈmɛndən/ is a calcium sensitiser used in the management of acutely decompensated congestive heart failure. It is marketed under the trade name Simdax (Orion Corporation).

Mechanism of action[edit]

Levosimendan is a calcium sensitizer — it increases the sensitivity of the heart to calcium, thus increasing cardiac contractility without a rise in intracellular calcium. Levosimendan exerts its positive inotropic effect by increasing calcium sensitivity of myocytes by binding to cardiac troponin C in a calcium-dependent manner. It also has a vasodilatory effect, by opening adenosine triphosphate (ATP)-sensitive potassium channels in vascular smooth muscle to cause smooth muscle relaxation. The combined inotropic and vasodilatory actions result in an increased force of contraction, decreased preload and decreased afterload. Moreover, by opening also the mitochondrial (ATP)-sensitive potassium channels in cardiomyocytes, the drug exerts a cardioprotective effect.[1]

Clinical use[edit]

Indications[edit]

Levosimendan is indicated for inotropic support in acutely-decompensated severe congestive heart failure.

Some of the Phase III studies in the extensive clinical program were the trials LIDO (200 patients), RUSSLAN (500), CASINO (250), REVIVE-I (100), REVIVE-II (600) and SURVIVE (1350). In total, the clinical data base includes more than 3500 patients in Phase IIb and III double-blind studies.[2]

In the SURVIVE study, despite a reduction in plasma B-type natriuretic peptide level in patients in the levosimendan group compared with patients in the dobutamine group, levosimendan did not significantly reduce all-cause mortality at 180 days.[3] However, the drug was proven to be superior to dobutamine for treating patients with a history of CHF or those on beta-blocker therapy when they are hospitalized with acute decompensations.[3]

In a meta-analysis of randomized controlled studies by Landoni et al. levosimendan is shown to reduce mortality and hospitalization.[4]

Licensing status[edit]

The Orion Corporation originally developed levosimendan and applied for a new drug application in 1998 in the U.S. However the Food and Drug Administration (FDA) requested further trials be conducted and Orion withdrew the application in November 1999. Initially, Orion obtained the approval to market the drug in Sweden in 2000.[5] Since then 60 countries worldwide have approved the drug but it remains non licensed in the USA, where it is currently under development for reduction in morbidity and mortality of cardiac surgery patients at risk of low cardiac output syndrome.[6]

Contraindications[edit]

The use of levosimendan is contraindicated in patients with: moderate-to-severe renal impairment, severe hepatic impairment, severe ventricular filling or outflow obstruction, severe hypotension and tachycardia, and/or history of torsades de pointes (Rossi, 2006).[7]

Adverse effects[edit]

Common adverse drug reactions (≥1% of patients) associated with levosimendan therapy include: headache, hypotension, arrhythmias (atrial fibrillation, extrasystoles, atrial tachycardia, ventricular tachycardia), myocardial ischaemia, hypokalaemia and/or nausea (Rossi, 2006).

Formulations[edit]

Levosimendan is marketed as a 2.5 mg/mL concentrated solution for IV infusion. The concentrate is diluted with glucose 5% solution before infusion.

References[edit]

  1. ^ Papp, Z; Édes, I; Fruhwald, S; De Hert, SG; Salmenperä, M; Leppikangas, H; Mebazaa, A; Landoni, G; Grossini, E; Caimmi, P; Morelli, A; Guarracino, F; Schwinger, RH; Meyer, S; Algotsson, L; Wikström, BG; Jörgensen, K; Filippatos, G; Parissis, JT; González, MJ; Parkhomenko, A; Yilmaz, MB; Kivikko, M; Pollesello, P; Follath, F (23 August 2012). "Levosimendan: Molecular Mechanisms and Clinical Implications: Consensus of Experts on the Mechanisms of Action of Levosimendan". International Journal of Cardiology. 159 (2): 82–7. doi:10.1016/j.ijcard.2011.07.022. PMID 21784540. 
  2. ^ Nieminen, MS; Fruhwald, S; Heunks, LM; Suominen, PK; Gordon, AC; Kivikko, M; Pollesello, P (2013). "Levosimendan: Current Data, Clinical Use and Future Development". Heart, Lung and Vessels. 5 (4): 227–45. PMC 3868185free to read. PMID 24364017. 
  3. ^ a b Mebazaa, A; Nieminen, MS; Packer, M; Cohen-Solal, A; Kleber, FX; Pocock, SJ; Thakkar, R; Padley, RJ; Põder, P; Kivikko, M; SURVIVE, Investigators (2 May 2007). "Levosimendan vs Dobutamine for Patients with Acute Decompensated Heart Failure: the SURVIVE Randomized Trial". JAMA. 297 (17): 1883–91. doi:10.1001/jama.297.17.1883. PMID 17473298. 
  4. ^ Landoni, G; Biondi-Zoccai, G; Greco, M; Greco, T; Bignami, E; Morelli, A; Guarracino, F; Zangrillo, A (February 2012). "Effects of Levosimendan on Mortality and Hospitalization. A Meta-analysis of Randomized Controlled Studies". Critical Care Medicine. 40 (2): 634–46. doi:10.1097/ccm.0b013e318232962a. PMID 21963578. 
  5. ^ Orion. "Simdax (levosimendan) Fact Sheet" (PDF). Orion. Retrieved 16 February 2013. 
  6. ^ OxygenBiotherapeutics. "Product Pipeline - Levosimendan development". OxygenBiotherapeutics. Retrieved 13 February 2013. 
  7. ^ Rossi S, editor. Australian Medicines Handbook 2006. Adelaide: Australian Medicines Handbook; 2006.