Brincidofovir

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Brincidofovir
Clinical data
Trade namesTembexa
Other namesCMX001; Cidofovir-HDP; hexadecyloxypropyl-cidofovir
License data
Routes of
administration
By mouth
ATC code
Legal status
Legal status
Identifiers
  • ({[(2S)-1-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-3-hydroxypropan-2-yl]oxy}methyl)[3-(hexadecyloxy)propoxy]phosphinic acid
JSmol)
  • CCCCCCCCCCCCCCCCOCCCOP(=O)(O)CO[C@H](CO)Cn1ccc(N)nc1=O
  • InChI=1S/C27H52N3O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-35-20-16-21-37-38(33,34)24-36-25(23-31)22-30-18-17-26(28)29-27(30)32/h17-18,25,31H,2-16,19-24H2,1H3,(H,33,34)(H2,28,29,32)/t25-/m0/s1
  • Key:WXJFKKQWPMNTIM-VWLOTQADSA-N

Brincidofovir, sold under the brand name Tembexa, is an

dsDNA viruses, as well as oral bioavailability.[4]

The most common side effects include diarrhea, nausea, vomiting, and abdominal pain.[2] It carries an FDA-mandated black box warning of an increased risk of death with extended use.[5][6] Brincidofovir was approved for medical use in the United States in June 2021.

Medical uses

Brincidofovir is indicated for the treatment of human smallpox disease caused by variola virus.[2][7]

Mechanism of action

Brincidofovir is a

conjugated with a lipid molecule. The lipid aspect of the molecule takes on the action of endogenous lysophosphatidyl choline, which then is able to enter cells in the body which are infected with smallpox.[8] Once the infected cell takes in the drug, the drug cleaves to generate cidofovir. Cidofovir is then consequently phosphorylated to yield cidofovir diphosphate, which is the active drug. Cidofovir diphosphate inhibits the variola virus' DNA polymerase-mediated DNA synthesis. The drug acts as an acyclic nucleotide and incorporates itself into the viral DNA chain, which then stops viral DNA synthesis.[9]

Pharmacokinetics

The oral bioavailability of Brincidofovir is 13.4% as a tablet and 16.8% in a suspension.[8] The metabolism of the drug is as such: once the drug enters the target infected cell, Brincidofovir's phosphodiester bond is then hydrolyzed to generate cidofovir which is then phosphorylated to the active cidofovir diphosphate. The volume of distribution of the drug is 1230 L.[8]

History

Because smallpox is eradicated, the effectiveness of brincidofovir was studied in animals infected with viruses that are closely related to the variola virus.[2] Effectiveness was determined by measuring animals' survival at the end of the studies.[2]

Safety information to support approval of brincidofovir was derived from clinical trials of the drug for a non-smallpox indication, primarily from patients who received hematopoietic stem cell transplants.[2]

The U.S.

fast track, and orphan drug designations.[2] The FDA approved brincidofovir under the agency's Animal Rule, which allows findings from adequate and well-controlled animal efficacy studies to serve as the basis of an approval when it is not feasible or ethical to conduct efficacy trials in humans.[2]

Expanded access ethical considerations

Brincidofovir (CMX001) was the subject of widespread

adverse events are more likely during these programs, because the people seeking access are usually much sicker than most, and problems experienced by these people can result in an unfavorable and inaccurate perception of the drug's safety profile.[10] In this case, the boy recovered from the infection in 2014, and died in 2016 from complications of cancer.[11]

Brincidofovir is one of several experimental drugs administered to a small number of patients to treat Ebola virus disease during the 2014 outbreak. The WHO published a report on the ethics of using unregistered interventions to treat Ebola, where they concluded that "In the particular context of the current Ebola outbreak in West Africa, it is ethically acceptable to offer unproven interventions that have shown promising results in the laboratory and in animal models but have not yet been evaluated for safety and efficacy in humans as potential treatment or prevention."[12]

Research

Brincidofovir is under investigation for the treatment of

monkeypox.[14]

Adenovirus and cytomegalovirus

As of 2014[update], brincidofovir is in

kidney transplants. Brincidofovir is not yet FDA approved for adenovirus or cytomegalovirus due to lack of efficacy in clinical trials.[16] In a trial of brincidofovir for patients with CMV brincidofovir was associated with a 15.5% week 24 all-cause mortality compared with 10.1% among placebo recipients. Additionally brincidofovir was associated with increased serious adverse events (57.1% versus 37.6%) compared with placebo.[16] Brincidofovir was initially offered via an FDA expanded access trial; however as of May 9, 2019, Chimerix discontinued clinical trials of brincidofovir for the treatment of adenovirus and discontinued the expanded access program in 2019.[17]

Ebola

After initial studies by the Centers for Disease Control and Prevention (CDC, Atlanta, Georgia, US) in cell culture models,

Ebola virus disease outbreak in the US in 2014.[19][20] The patient was given the drug starting six days after hospital admission when he was already critically ill; he died four days later.[21][22] Brincidofovir was also given to Ebola patient Ashoka Mukpo at the Nebraska Medical Center, who had developed the disease and then was pronounced Ebola-free and released from the center on 22 October 2014.[23]

In October 2014, Chimerix reported it had been given approval by the FDA to start Phase 2 trials in patients infected with ebolaviruses for brincidofovir's safety, tolerability, and efficacy.

Oxford University and Médecins Sans Frontières planned to extend the trial to Sierra Leone, where there were still Ebola cases; but on 30 January 2015, the manufacturer decided to withdraw support for the trial and end discussion of future trials.[27][28]

Animals

In animal trials brincidofovir has shown activity against cytomegalovirus,

Ebola virus disease, which is somewhat paradoxical, as ebolaviruses are RNA viruses and thus do not contain DNA as the above-mentioned viruses.[18][30]

References

  1. FDA
    . Retrieved 22 October 2023.
  2. ^ a b c d e f g h "FDA approves drug to treat smallpox". U.S. Food and Drug Administration (FDA). 4 June 2021. Archived from the original on 8 June 2021. Retrieved 7 June 2021. Public Domain This article incorporates text from this source, which is in the public domain.
  3. ^ a b "Brincidofovir (CMX001)". Chimerix. Archived from the original on 20 March 2014.
  4. S2CID 25854860
    .
  5. ^ "FDA Tembexa Product Insert" (PDF).
  6. ^ "DailyMed - TEMBEXA- brincidofovir tablet, film coated". dailymed.nlm.nih.gov.
  7. ^ Birnkrant D (4 June 2021). "Brincidofovir: NDA Approval – Animal Efficacy" (PDF). Center for Drug Evaluation and Research. U.S. Food and Drug Administration. Archived (PDF) from the original on 8 June 2021. Retrieved 8 June 2021.
  8. ^ a b c "Brincidofovir". go.drugbank.com. Archived from the original on 2 December 2021. Retrieved 7 June 2022.
  9. ^ Patient Information (approved by the U.S. Food and Drug Administration)
  10. ^
    PMID 25587952
    .
  11. ^ "Josh Hardy, Va. Boy Who Inspired Social Media Campaign, Dies". NBC4 Washington. 22 October 2016. Archived from the original on 22 May 2018. Retrieved 21 May 2018.
  12. ^ Report of an advisory panel to WHO. "Ethical considerations for use of unregistered interventions for Ebola virus disease". Archived from the original on 23 August 2014. Retrieved 8 October 2014.
  13. PMID 21499452
    .
  14. .
  15. ^ "Brincidofovor for Ebola". Chimerix. Archived from the original on 9 October 2014.
  16. ^
    PMID 30292744
    .
  17. ^ "Chimerix Expanded Access". Chimerix, Inc. Archived from the original on 2 December 2020. Retrieved 24 September 2020.
  18. ^
    PMID 26526586
    .
  19. ^ "Chimerix Announces Emergency Investigational New Drug Applications for Brincidofovir Authorized by FDA for Patients With Ebola Virus Disease". Archived from the original on 6 October 2014. Retrieved 8 October 2014.
  20. ^ Almendrala A (6 October 2014). "Dallas Ebola Patient Receives Experimental Drug". The Huffington Post. Archived from the original on 3 December 2014. Retrieved 8 October 2014.
  21. ^ Berman M, Brown DL (8 October 2014). "Thomas Duncan, the Texas Ebola patient, has died". Washington Post. Archived from the original on 9 October 2014. Retrieved 8 October 2014.
  22. ^ Cohen E (7 October 2014). "Dallas Ebola patient waited nearly a week for experimental drug; family claims bias". CNN. Archived from the original on 2 December 2014. Retrieved 8 October 2014.
  23. ^ Wilson T (22 October 2014). "Young and Healthy: How NBC News Freelancer Ashoka Mukpo Survived Ebola". NBC News. Archived from the original on 26 December 2017. Retrieved 26 December 2017.
  24. ^ Loftus P (16 October 2014). "Chimerix to Conduct Ebola Drug Trial: Drug Company Gets FDA Approval to Start Trial Immediately in Infected Patients". The Wall Street Journal. Archived from the original on 14 March 2016. Retrieved 13 March 2017.
  25. from the original on 11 March 2020. Retrieved 16 March 2020.
  26. ^ Giahyue JH (6 January 2015). "Trials of untested Ebola drugs begin in West Africa". Reuters. Archived from the original on 9 January 2015. Retrieved 6 January 2015.
  27. ^ Kroll D (31 January 2015). "Chimerix Ends Brincidofovir Ebola Trials to Focus on Adenovirus and CMV". Forbes. Archived from the original on 8 July 2018. Retrieved 31 January 2015.
  28. ^ "Ebola drug trial in Liberia halted". Médecins Sans Frontières. 3 February 2015. Archived from the original on 20 March 2015. Retrieved 7 March 2015.
  29. PMID 20923374
    .
  30. ^ David Kroll (7 October 2014). "Chimerix's Brincidofovir Given To Dallas, Nebraska Ebola Patients". forbes.com. Archived from the original on 28 July 2016. Retrieved 25 August 2017.

Further reading

External links