Evidence map›Paper›PMID 26953200›Full record

ArticleAntimicrobial agents and chemotherapy2016

Evaluation of Drug-Drug Interactions between Direct-Acting Anti-Hepatitis C Virus Combination Regimens and the HIV-1 Antiretroviral Agents Raltegravir, Tenofovir, Emtricitabine, Efavirenz, and Rilpivirine.

Amit Khatri, Sandeep Dutta, Martin Dunbar, Thomas Podsadecki, Roger Trinh, Walid Awni, Rajeev Menon

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Combined Oral Contraceptives As Victims of Drug Interactions.Drug metabolism and disposition: the biological fate of chemicals · 2023
    Review
  5. Review
  6. Observational
  7. Article
  8. Article
  9. Article
  10. Clinical Pharmacokinetics of Ombitasvir.Clinical pharmacokinetics · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. HIV/HCV Antiviral Drug Interactions in the Era of Direct-acting Antivirals.Journal of clinical and translational hepatology · 2016
    Review
  15. Article
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Amit KhatriAbbVie, Inc., Research and Development, North Chicago, Illinois, USA amit.khatri@abbvie.com.
Sandeep DuttaAbbVie, Inc., Research and Development, North Chicago, Illinois, USA.
Martin DunbarAbbVie, Inc., Research and Development, North Chicago, Illinois, USA.
Thomas PodsadeckiAbbVie, Inc., Research and Development, North Chicago, Illinois, USA.
Roger TrinhAbbVie, Inc., Research and Development, North Chicago, Illinois, USA.
Walid AwniAbbVie, Inc., Research and Development, North Chicago, Illinois, USA.
Rajeev MenonAbbVie, Inc., Research and Development, North Chicago, Illinois, USA.
AbbVie (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The three direct-acting antiviral agent (3D) regimen is a novel combination of direct-acting antiviral agents (DAAs) that has proven effective for the treatment of hepatitis C virus (HCV) infection. Given the potential for coadministration in patients with human immunodeficiency virus infection, possible drug interactions with antiretroviral drugs must be carefully considered. Four phase 1, multiple-dose pharmacokinetic studies were conducted in healthy volunteers (n = 66). The 3D regimen of 150/100 mg daily paritaprevir/ritonavir, 25 mg daily ombitasvir, and 400 mg twice-daily dasabuvir was administered alone or in combination with 200 mg daily of emtricitabine and 300 mg daily of tenofovir disoproxil fumarate (tenofovir DF), 25 mg daily of rilpivirine, or 400 mg of raltegravir twice daily. A 2-DAA regimen of 150/100 mg daily paritaprevir/ritonavir and 400 mg of dasabuvir twice daily was also studied in combination with efavirenz/emtricitabine/tenofovir DF at 600/200/300 mg daily, respectively (Atripla; Bristol-Myers Squibb). Pharmacokinetic parameters were determined from plasma drug concentrations. No clinically significant drug interactions were observed (≤32% change in exposure) between the 3D regimen and that of emtricitabine plus tenofovir DF. Raltegravir exposure was increased up to 134% when the drug was coadministered with the 3D regimen. Although coadministration with rilpivirine was well tolerated in healthy volunteers, observed elevations in rilpivirine exposures may increase the potential for adverse drug reactions. Concomitant use of the 2-DAA regimen and efavirenz/emtricitabine/tenofovir DF was discontinued owing to poor tolerability and adverse events. No dose adjustment is required during coadministration of raltegravir, tenofovir DF, or emtricitabine with the 3D regimen. Rilpivirine is not recommended and efavirenz is contraindicated for coadministration with the 3D regimen.

Indexed as

AlkynesAnti-Retroviral AgentsAntiviral AgentsBenzoxazinesCyclopropanesDrug InteractionsEmtricitabineHepacivirusHIV-1HumansRaltegravir PotassiumRilpivirineTenofovirAlkynesAnti-Retroviral AgentsAntiviral AgentsBenzoxazinesCyclopropanesefavirenzEmtricitabineRaltegravir PotassiumRilpivirineTenofovir

Identifiers

PMID26953200
PMCPMC4862503
OpenAlexW2297615718

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.