Tolvaptan
Clinical data | |
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Trade names | Samsca |
Other names | N-{4-[(6R)-9-chloro-6-hydroxy-2-azabicyclo[5.4.0]undeca-8,10,12-triene-2-carbonyl]-3-methyl-phenyl}-2-methyl-benzamide |
AHFS/Drugs.com | Monograph |
MedlinePlus | a609033 |
License data | |
Routes of administration | Oral |
ATC code | |
Legal status | |
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Pharmacokinetic data | |
Bioavailability | Unknown (40% absorbed) |
Protein binding | 99% |
Metabolism | Hepatic (CYP3A4-mediated)[2] |
Elimination half-life | 12 hours (terminal) |
Identifiers | |
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CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
ChemSpider | |
UNII | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.219.212 |
Chemical and physical data | |
Formula | C26H25ClN2O3 |
Molar mass | 448.941 g/mol g·mol−1 |
3D model (JSmol) | |
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Tolvaptan (INN), also known as OPC-41061, is a selective, competitive vasopressin receptor 2 antagonist used to treat hyponatremia (low blood sodium levels) associated with congestive heart failure, cirrhosis, and the syndrome of inappropriate antidiuretic hormone (SIADH). Tolvaptan was approved by the U.S. Food and Drug Administration on May 19, 2009, and is sold by Otsuka Pharmaceutical Co. under the trade name Samsca and in India is sold by MSN laboratories LTD under the trade name Tolvat & Tolsama and by SUN PHARMA under the trade name NATRISE. Tolvaptan is also in fast-track clinical trials[3] for polycystic kidney disease. In a 2004 trial, tolvaptan, when administered with traditional diuretics, was noted to increase excretion of excess fluids and improve blood sodium levels in patients with heart failure without producing side effects such as hypotension (low blood pressure) or hypokalemia (decreased blood levels of potassium) and without having an adverse effect on kidney function.[4] In a recently published trial (TEMPO 3:4 ClinicalTrials.gov number, NCT00428948) the study met its primary and secondary end points. Tolvaptan, when given at an average dose of 95 mg per day over a 3-year period, slowed the usual increase in kidney volume by 50% compared to placebo (2.80% per year versus 5.51% per year, respectively, p<0.001) and reduced the decline in kidney function when compared with that of placebo-treated patients by approximately 30% (reciprocal serum creatinine, -2.61 versus -3.81 (mg/mL)-1 per year, p <0.001)[5]
Chemistry
Chemical synthesis:[6]
Side effects
The FDA has warned of potential liver injury with the drug.[7]
References
- ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
- ^ Shoaf S, Elizari M, Wang Z; et al. (2005). "Tolvaptan administration does not affect steady state amiodarone concentrations in patients with cardiac arrhythmias". J Cardiovasc Pharmacol Ther. 10 (3): 165–71. doi:10.1177/107424840501000304. PMID 16211205.
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(help)CS1 maint: multiple names: authors list (link) - ^ Otsuka Maryland Research Institute, Inc.
- ^ Gheorghiade M, Gattis W, O'Connor C; et al. (2004). "Effects of tolvaptan, a vasopressin antagonist, in patients hospitalized with worsening heart failure: a randomized controlled trial". JAMA. 291 (16): 1963–71. doi:10.1001/jama.291.16.1963. PMID 15113814.
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(help)CS1 maint: multiple names: authors list (link) - ^ (2012) Tolvaptan in Patients with Autosomal Dominant Polycystic Kidney Disease
- ^ Kondo, K.; Ogawa, H.; Yamashita, H.; Miyamoto, H.; Tanaka, M.; Nakaya, K.; Kitano, K.; Yamamura, Y.; Nakamura, S.; Onogawa, T.; et al.; Bioor. Med. Chem. 1999, 7, 1743.
- ^ 2013 MedPage Today http://www.medpagetoday.com/Nephrology/GeneralNephrology/37000
- Gheorghiade M, Niazi I, Ouyang J; et al. (2003). "Vasopressin V2-receptor blockade with tolvaptan in patients with chronic heart failure: results from a double-blind, randomized trial". Circulation. 107 (21): 2690–6. doi:10.1161/01.CIR.0000070422.41439.04. PMID 12742979.
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