Chemistry:Mipomersen

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Short description: Drug used to treat genetic hypercholesterolemia
Mipomersen
Mipomersen sodium colored.svg
Clinical data
Trade namesKynamro
Other namesISIS 301012
AHFS/Drugs.comMultum Consumer Information
Pregnancy
category
  • US: B (No risk in non-human studies)
Routes of
administration
Subcutaneous injection
ATC code
Legal status
Legal status
Pharmacokinetic data
Protein binding≥90%
MetabolismNucleases
Elimination half-life1–2 months
Excretion<4% in urine in 24 hours
Identifiers
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC230H305N67Na19O122P19S19
Molar mass7594.76 g·mol−1

Mipomersen (INN; trade name Kynamro) is a drug used to treat homozygous familial hypercholesterolemia and is administered by subcutaneous injection. There is a serious risk of liver damage from this drug and it can only be prescribed in the context of a risk management plan.

Indications

Kynamro is used to treat homozygous familial hypercholesterolemia and is administered by injection.[1][2]

It cannot be freely prescribed; instead every person put on mipomersen is enrolled in a Risk Evaluation and Mitigation Strategies (REMS) program approved by the FDA.[1]

Pregnancy and lactation

Mipomersen is pregnancy category B; women who are pregnant or intending to become pregnant should only use this drug if needed. It is unknown if it is secreted in human breast milk, but it was found to be secreted in the breast milk of rats.[1]

Contraindications

The drug is contraindicated in people with moderate to severe liver impairment, active liver diseases, and unexplained high levels of transaminase liver enzymes.[1][3]

Adverse effects

The drug has a black box warning about the risk of liver damage; specifically it can cause elevations in the levels of transaminases and causes fatty liver disease.[1]

In clinical trials, 18% of subjects taking mipomersen stopped using the drug due to adverse effects; the most common adverse effects leading to discontinuation were injection site reactions, increases of transaminases, flu-like symptoms (fever, chills, abdominal pain, nausea, vomiting), and abnormal liver tests.[1]

Other adverse effects include: heart problems including angina and palpitations, edema, pain in legs or arms, headache, insomnia, and hypertension.[1]

Interactions

Other drugs known for causing liver problems might add to mipomersen's risk of liver damage. No pharmacokinetic interactions have been described.[3]

Pharmacology

Mechanism of action

Mipomersen binds to the messenger RNA coding for apolipoprotein B-100 (ApoB-100), a protein that is the main component of low-density lipoprotein (LDL) and very low-density lipoprotein (VLDL). As a consequence, the RNA is degraded by the enzyme ribonuclease H, and ApoB-100 is not translated.[3]

Pharmacokinetics

After subcutaneous injection, mipomersen reaches highest blood levels after 3 to 4 hours. It accumulates in the liver,[citation needed] which is convenient since apolipoprotein B predominantly acts there. Protein binding is over 90%. The molecule is slowly broken up by endonucleases and subsequently by exonucleases. After 24 hours, less than 4% of the degradation products are found in the urine, and overall half-life is 1 to 2 months.[3]

Chemistry

Chemical structure[4]:69
Complete skeletal formula[1]:10

The compound is a 'second-generation' antisense oligonucleotide; the nucleotides are linked with phosphorothioate linkages rather than the phosphodiester linkages of RNA and DNA, and the sugar parts are deoxyribose in the middle part of the molecule and 2’-O-methoxyethyl-modified ribose at the two ends. These modifications make the drug resistant to degradation by nucleases, allowing it to be administered weekly.

The complete sequence is portrayed below:[5][1]:10

5’—G*—mC*—mC*—mU*—mC*—dAdGdT—dmC—dTdG—dmC—dTdT—dmC—G*—mC*—A*—mC*—mC*—3’
* = 2’-O-(2-methoxyethyl)
m = 5-methyl
d = 2’-deoxy

History

The drug was discovered and developed to Phase 2 by Ionis Pharmaceuticals and subsequently licensed to Genzyme Corporation in 2008 by an auction bid. Ionis earned an upfront payment of $325 million, with payments of a further $825 million if milestones are met.[6]

Mipomersen was rejected by the European Medicines Agency in 2012[7] and again in 2013 due to concerns about the liver and cardiovascular adverse effects.[8]

In January 2013, The United States Food and Drug Administration approved mipomersen for the treatment of homozygous familial hypercholesterolemia.[9][10]

References

  1. 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 "Kynamro (mipomersen sodium) Injection, Solution for Subcutaneous Injection. Full Prescribing Information". Kastle Therapeutics, Chicago, IL. http://www.kynamro.com/media/pdfs/Kynamro_Prescribing_information.pdf. 
  2. "Cholesterol Lowering Drugs". Endotext [Internet]. South Dartmouth (MA): MDText.com, Inc.. August 10, 2016. https://www.ncbi.nlm.nih.gov/books/NBK395573/. 
  3. 3.0 3.1 3.2 3.3 Drugs.com: Mipomersen Professional Drug Facts.
  4. "International Nonproprietary Names for Pharmaceutical Substances (INN). Recommended International Nonproprietary Names: List 61". World Health Organization. 2009. https://www.who.int/medicines/publications/druginformation/innlists/RL61.pdf. 
  5. "Clinical and preclinical pharmacokinetics and pharmacodynamics of mipomersen (kynamro(®)): a second-generation antisense oligonucleotide inhibitor of apolipoprotein B". Clinical Pharmacokinetics 54 (2): 133–146. February 2015. doi:10.1007/s40262-014-0224-4. PMID 25559341. 
  6. "Genzyme and Isis Complete Licensing of Mipomersen". FreshNews.com. 24 June 2008. http://www.freshnews.com/news/74972/genzyme-and-isis-complete-licensing-mipomersen. 
  7. "EMA committee shoots down Sanofi's cholesterol drug mipomersen". FierceBiotech. December 14, 2012. http://www.fiercebiotech.com/regulatory/ema-committee-shoots-down-sanofi-s-cholesterol-drug-mipomersen. 
  8. "Refusal of the marketing authorisation for Kynamro (mipomersen)". European Medicines Agency (EMA). March 21, 2013. http://www.ema.europa.eu/docs/en_GB/document_library/Summary_of_opinion_-_Initial_authorisation/human/002429/WC500140678.pdf. 
  9. "F.D.A. Approves Genetic Drug to Treat Rare Disease". The New York Times. 29 January 2013. https://www.nytimes.com/2013/01/30/business/fda-approves-genetic-drug-to-treat-rare-disease.html. 
  10. "FDA approves new orphan drug Kynamro to treat inherited cholesterol disorder". U.S. Food and Drug Administration. 29 January 2013. https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm337195.htm.