Apricitabine

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Apricitabine
Clinical data
Routes of
administration		Oral
ATC code
  • none
Legal status
Legal status
  • Investigational
Pharmacokinetic data
Bioavailability65 to 80%
Protein binding< 4%
MetabolismTo apricitabine triphosphate
Elimination half-life6 to 7 hours (triphosphate)
ExcretionRenal
Identifiers
  • 4-amino-1-[(2R,4R)-2-(hydroxymethyl)-1,3- oxathiolan-4-yl]pyrimidin-2(1H)-one
JSmol)
  • O=C1/N=C(/N)\C=C/N1[C@@H]2S[C@@H](OC2)CO
  • InChI=1S/C8H11N3O3S/c9-5-1-2-11(8(13)10-5)6-4-14-7(3-12)15-6/h1-2,6-7,12H,3-4H2,(H2,9,10,13)/t6-,7-/m1/s1 checkY
  • Key:RYMCFYKJDVMSIR-RNFRBKRXSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Apricitabine (

analogue of cytidine
.

History

It was first developed by BioChem Pharma (where it was called BCH10618). BioChem Pharma was then sold to

United States Food and Drug Administration.[3]

Avexa announced its decision to end work on apricitabine in May 2010, which Avexa spent more than A$100 million ($90 million) developing and was in the final of three stages of patient studies usually needed for U.S. regulatory approval. Grounds for the shutdown included the inability to find commercial partners for global licensing, concerns about legal protections of the drug in the US market, and difficulty confirming the effectiveness of the drug in patients where other retroviral drugs masked key indicators.[4]

In March 2011 it was announced by the company to the

Australian Stock Exchange that the FDA had agreed that a new, shorter, single Phase III trial design, including about 300 patients dosed for 2 weeks, was required before approval. A similar agreement with the EMA was announced in March 2012.[5]

In November 2011 the company sought to extend its patents over apricitabine and was in discussions for fast-track approval with European regulators. The company also indicated that clinical trials had shown better-than-expected results from simultaneous provision of the drug alongside two other marketed drugs when compared to those drugs with lamivudine, another NRTI.[6]

Avexa's latest update in 2013 reported that the drug was still in phase IIb trials and had not yet started phase III.[7]

Dosage

As a monotherapy, 1200 mg apricitabine per day reduced the viral load by up to 1.65 logs (45 fold) in a small, 10-day randomized controlled trial.[8] An 800 mg dose twice a day is being used in later studies.

Adverse effects

Apricitabine appears to be well tolerated. The most common

bone marrow suppression, or liver and kidney toxicity.[9]
No patients in either study had to stop taking apricitabine because of side effects.

Drug resistance

In vitro, apricitabine is effective against NRTI-(lamivudine and zidovudine)-resistant virus strains, including M184V and multiple thymidine analogue mutations (TAMs).

In early studies, no mutations causing drug resistance were observed. Newer trials showed that apricitabine may induce K65R mutations, resulting in resistance against

tenofovir.[1]

In clinical studies, apricitabine has been good at reducing viral loads while apparently producing little selection pressure, resulting in the addition of no further mutations in treatment-experienced patients with common pre-existing mutations, including M184V or K65R or TAMs (M41L, M184V, and T215Y).[10]

References

  1. ^ a b "Apricitabine". AIDSmeds.com. Archived from the original on March 21, 2008.
  2. ^ Avexa Closes ATC's Phase III Trial To Evaluate Data
  3. ^ "Apricitabine". AIDSinfo. U.S. National Institutes of Health. March 13, 2007. Archived from the original on June 5, 2011. Retrieved 2008-08-29.
  4. ^ "Avexa closes apricitabine (ATC) program" (PDF). Avexa Company Announcement. Archived from the original (PDF) on August 21, 2011.
  5. ^ "Avexa and FDA agree path forward for ATC" (PDF). Avexa. Archived from the original (PDF) on March 20, 2012.
  6. ^ Avexa Company Announcement to Australian Stock Exchange: Avexa files to extend ATC patent life
  7. ^ "Update on apricitabine's Clinical Development" (PDF). 2013-09-14. Archived from the original (PDF) on 2014-02-25. Retrieved 2014-04-09.
  8. ^
    S2CID 19607533
    .
  9. ^ Cox S, Moore S, Southby J, Alsumde A (August 5, 2008). Safety profile of apricitabine, a novel NRTI, during 24-week dosing in experienced HIV-1 infected patients. XVII International AIDS Conference (AIDS 2008). Mexico City. Abstract TUAB0106. Archived from the original on July 24, 2011. Retrieved 2008-08-29. Lay summary
  10. PMID 19223637
    .
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