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Doravirine/lamivudine/tenofovir

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Doravirine/lamivudine/tenofovir
Combination of
DoravirineNon-nucleoside reverse transcriptase inhibitor
LamivudineNucleoside reverse transcriptase inhibitor
Tenofovir disoproxilNucleotide reverse transcriptase inhibitor
Clinical data
Trade namesDelstrigo
Other namesMK-1439A
AHFS/Drugs.comMonograph
MedlinePlusa618049
License data
ATC code
Legal status
Legal status
Identifiers
KEGG

Doravirine/lamivudine/tenofovir disoproxil (brand name Delstrigo) is a fixed-dose combination drug for the treatment of HIV/AIDS.[2][3] It contains doravirine, lamivudine, and tenofovir disoproxil.[4][3] In the United States, it was approved by the Food and Drug Administration (FDA) in August 2018, for the treatment of HIV-1 infection.[4][5]

References

  1. ^ "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 October 2023.
  2. ^ "Doravirine/lamivudine/tenofovir disoproxil fumarate". Adis Insight.
  3. ^ a b Canadian Agency for Drugs and Technologies in Health (June 2019). "Common Drug Review New Combination Product: Doravirine/Lamivudine/Tenofovir Disoproxil Fumarate Fixed-Dose Combination (Delstrigo)". CADTH Common Drug Reviews. Ottawa (ON). PMID 31393687.
  4. ^ a b "FDA Approves Merck's DELSTRIGO (doravirine / lamivudine / tenofovir disoproxil fumarate), a Once-Daily Fixed-Dose Combination Tablet as a Complete Regimen and PIFELTRO (doravirine), an NNRTI, Both for the Treatment of HIV-1 in Appropriate Patients" (Press release). Merck & Co. 30 August 2018.
  5. ^ "Delstrigo approval letter" (PDF). Food and Drug Administration (FDA). 30 August 2018. Retrieved 10 September 2019.

External links