Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Dapivirine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Dapivirine
Clinical data
ATC code
Identifiers
  • 4-{[4-(Mesitylamino)-2-pyrimidinyl]amino}benzonitrile
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.214.755Edit this at Wikidata
Chemical and physical data
FormulaC20H19N5
Molar mass329.398
3D model (JSmol)
  • Cc1cc(c(c(c1)C)Nc2ccnc(n2)Nc3ccc(cc3)C#N)C
  • InChI=1S/C20H19N5/c1-13-10-14(2)19(15(3)11-13)24-18-8-9-22-20(25-18)23-17-6-4-16(12-21)5-7-17/h4-11H,1-3H3,(H2,22,23,24,25)
  • Key:ILAYIAGXTHKHNT-UHFFFAOYSA-N

Dapivirine is a non-nucleosidereverse transcriptase inhibitor developed at Janssen Therapeutics (formerlyTibotec Therapeutics).[1] TheInternational Partnership for Microbicides has held exclusive worldwide rights to dapivirine since 2014,[2] building upon a 2004 royalty-free license to develop dapivirine-based microbicides for women in resource-poor countries.[3]

A monthlyintravaginal ring containing dapivirine has been developed as a way of preventing infection by human immunodeficiency virus in women. Two phase 3 clinical trials ofintravaginal dapivirine rings for HIV prevention were completed in 2015 and results were announced at the 2016Conference on Retroviruses and Opportunistic Infections. The ASPIRE Study (MTN-020) reported a 27% reduction in HIV-1 acquisition (95% CI 12-57%, p=0.007), with a trend toward greater protection in women over age 21 and no significant protection for women under age 21.[4] The Ring Study (IPM-027) reported a 31% reduction in HIV acquisition (95% CI 0.9-51.5%, p=0.040) also with a trend toward greater efficacy in women over age 21.[5] In both trials, more than 80% of returned rings showed signs of drug depletion indicating at least some use, and more than 80% of blood samples from participants in the active arm had levels of dapivirine consistent at least 8 hours of continuous use preceding the blood test. Neither trial could evaluate whether the product was used consistently between study visits.

As of December 2019, it became the first of its kind to be submitted for regulatory approval.[6][7]

External links

[edit]

References

[edit]
  1. ^"Johnson & Johnson to Acquire Tibotec-Virco (NYSE:JNJ)".www.investor.jnj.com. Archived fromthe original on 2016-05-08. Retrieved2016-04-13.
  2. ^hseltzer (8 May 2014)."IPM Receives Worldwide Rights to HIV Prevention Medicine".www.ipmglobal.org. Retrieved2016-04-13.
  3. ^ipm-admin (29 September 2010)."Dapivirine (TMC120)".www.ipmglobal.org. Retrieved2016-04-13.
  4. ^Baeten JM."A Phase III Trial of the Dapivirine Vaginal Ring for HIV-1 Prevention in Women". Retrieved2016-04-13.
  5. ^Nel A."Safety and Efficacy of Dapivirine Vaginal Ring for HIV-1 Prevention in African Women". Retrieved2016-04-13.
  6. ^PrEWatch.org."Nextgen-Dapivirine Vaginal Ring". Retrieved2020-05-26.
  7. ^ipmglobal.org (3 March 2016)."Dapivirine Ring". Retrieved2020-05-26.
Capsid inhibitors
Entry/fusion inhibitors
(Discovery and development)
Integrase inhibitors
(Integrase strand transfer inhibitors (INSTI))
Maturation inhibitors
Protease Inhibitors (PI)
(Discovery and development)
1st generation
2nd generation
Reverse-transcriptase
inhibitors
(RTIs)
Nucleoside and
nucleotide (NRTI)
Non-nucleoside (NNRTI)
(Discovery and development)
1st generation
2nd generation
Combined formulations
Pharmacokinetic boosters
Experimental agents
Uncoating inhibitors
Transcription inhibitors
Translation inhibitors
BNAbs
Other
Failed agents
°DHHSrecommendedinitial regimen options.Formerly or rarely used agent.


Stub icon

Thisdrug article relating to thegenito-urinary system is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Dapivirine&oldid=1182449644"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp