NDAORALTABLET
Approved
Aug 2018
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
1
Data completeness
6/8 — Strong
DELSTRIGO (doravirine, lamivudine, and tenofovir disoproxil fumarate) by Merck & Co. is non-nucleoside reverse transcriptase inhibitors [moa]. First approved in 2018.
Drug data last refreshed 19h ago · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
DELSTRIGO is a once-daily oral fixed-dose combination tablet containing doravirine (a non-nucleoside reverse transcriptase inhibitor), lamivudine, and tenofovir disoproxil fumarate for the treatment of HIV-1 infection. It works by inhibiting reverse transcriptase, a key enzyme in HIV replication. This combination therapy is designed for treatment-naive and treatment-experienced adult patients with HIV-1.
$16MPart D
Peak10.3 years to LOEProduct is in peak lifecycle stage with modest Part D adoption; brand team focuses on market penetration and clinical positioning in competitive HIV-1 therapy landscape.
Mechanism of Action
Non-Nucleoside Reverse Transcriptase Inhibitors
Pharmacologic Class:
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (1)
The Effect on Lipid Profile of Switching to Delstrigo in HIV Positive Patients
Started Nov 2023
19 enrolled
Hiv
Career Relevance
DELSTRIGO offers stable career opportunities in a mature HIV-1 franchise with established market presence and long patent protection. Professionals joining this product will focus on market share defense, payer negotiations, and clinical differentiation in a competitive therapeutic class.
Brand Manager
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.