Evidence map›Paper›PMID 26895022›Full record

ArticleClinical pharmacokinetics2016

Drug-Drug Interactions Between the Anti-Hepatitis C Virus 3D Regimen of Ombitasvir, Paritaprevir/Ritonavir, and Dasabuvir and Eight Commonly Used Medications in Healthy Volunteers.

Akshanth R Polepally, Jennifer R King, Bifeng Ding, Diana L Shuster, Emily O Dumas, Amit Khatri, Yi-Lin Chiu, Thomas J Podsadecki, Rajeev M Menon

Abstract readClinical Trial, Phase I
In one paragraph

Article in Clinical pharmacokinetics, 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
–field-weighted citation impact
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.

  1. Trial
  2. Article
  3. Article
  4. Hydrocodone, Oxycodone, and Morphine Metabolism and Drug-Drug Interactions.The Journal of pharmacology and experimental therapeutics · 2023
    Review
  5. Review
  6. Observational
  7. Observational
  8. Article
  9. Clinical Pharmacokinetics of Paritaprevir.Clinical pharmacokinetics · 2017
    Review
  10. Clinical Pharmacokinetics of Ombitasvir.Clinical pharmacokinetics · 2017
    Review
  11. Article
  12. Clinical Pharmacokinetics of Dasabuvir.Clinical pharmacokinetics · 2017
    Review
  13. Article
  14. Article
  15. Article
  16. Article
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

9 authors.

Akshanth R PolepallyClinical Pharmacokinetics and Pharmacodynamics, AbbVie Inc., Dept. R4PK, Bldg. AP31-3, 1 North Waukegan Road, North Chicago, IL, 60064, USA. akshanth.r.polepally@abbvie.com.
Jennifer R KingClinical Pharmacokinetics and Pharmacodynamics, AbbVie Inc., Dept. R4PK, Bldg. AP31-3, 1 North Waukegan Road, North Chicago, IL, 60064, USA.
Bifeng DingBiometrics, AbbVie Inc., Dept. R43V, Bldg. AP31-2, 1 North Waukegan Road, North Chicago, IL, 60064, USA.
Diana L ShusterClinical Pharmacokinetics and Pharmacodynamics, AbbVie Inc., Dept. R4PK, Bldg. AP31-3, 1 North Waukegan Road, North Chicago, IL, 60064, USA.
Emily O DumasInfectious Disease Development, AbbVie Inc., Dept. R48U, Bldg. AP30-3, 1 North Waukegan Road, North Chicago, IL, 60064, USA.
Amit KhatriClinical Pharmacokinetics and Pharmacodynamics, AbbVie Inc., Dept. R4PK, Bldg. AP31-3, 1 North Waukegan Road, North Chicago, IL, 60064, USA.
Yi-Lin ChiuBiometrics, AbbVie Inc., Dept. R43V, Bldg. AP31-2, 1 North Waukegan Road, North Chicago, IL, 60064, USA.
Thomas J PodsadeckiInfectious Disease Development, AbbVie Inc., Dept. R48U, Bldg. AP30-3, 1 North Waukegan Road, North Chicago, IL, 60064, USA.
Rajeev M MenonClinical Pharmacokinetics and Pharmacodynamics, AbbVie Inc., Dept. R4PK, Bldg. AP31-3, 1 North Waukegan Road, North Chicago, IL, 60064, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe three direct-acting antiviral regimen of ombitasvir/paritaprevir/ritonavir and dasabuvir (3D regimen) is approved for treatment of hepatitis C virus (HCV) genotype 1 infection. Drug-drug interaction (DDI) studies of the 3D regimen and commonly used medications were conducted in healthy volunteers to provide information on coadministering these medications with or without dose adjustments.

methodsThree phase I studies evaluated DDIs between the 3D regimen (ombitasvir/paritaprevir/ritonavir 25/150/100 mg once daily + dasabuvir 250 mg twice daily) and hydrocodone bitartrate/acetaminophen (5/300 mg), metformin hydrochloride (500 mg), diazepam (2 mg), cyclobenzaprine hydrochloride (5 mg), carisoprodol (250 mg), or sulfamethoxazole/trimethoprim (SMZ/TMP) (800/160 mg twice daily), all administered orally. DDI magnitude was determined using geometric mean ratios and 90 % confidence intervals for the maximum plasma concentration (C max) and area under the plasma concentration-time curve (AUC).

resultsChanges in exposures (C max and AUC geometric mean ratios) of acetaminophen, metformin, sulfamethoxazole, trimethoprim, and diazepam were ≤25 % upon coadministration with the 3D regimen. The C max and AUC of nordiazepam, an active metabolite of diazepam, increased by 10 % and decreased by 44 %, respectively. Exposures of cyclobenzaprine and carisoprodol decreased by ≤40 and ≤46 %, respectively, whereas exposures of hydrocodone increased up to 90 %. Ombitasvir, paritaprevir, ritonavir, and dasabuvir exposures changed by ≤25 %, except for a 37 % decrease in paritaprevir C max with metformin and a 33 % increase in dasabuvir AUC with SMZ/TMP.

conclusionsAcetaminophen, metformin, sulfamethoxazole, and trimethoprim can be coadministered with the 3D regimen without dose adjustment. Higher doses may be needed for diazepam, cyclobenzaprine, and carisoprodol based on clinical monitoring. A 50 % lower dose and/or clinical monitoring should be considered for hydrocodone. No dose adjustment is necessary for the 3D regimen.

Indexed as

2-NaphthylamineAdolescentAdultAnilidesAntiviral AgentsCarbamatesCyclopropanesDrug InteractionsDrug Therapy, CombinationFemaleHealthy VolunteersHepacivirusHepatitis C, ChronicHumansLactams, MacrocyclicMacrocyclic Compounds2-NaphthylamineAnilidesAntiviral AgentsCarbamatesCyclopropanesdasabuvirLactams, MacrocyclicMacrocyclic CompoundsombitasvirparitaprevirProlineRitonavirSulfonamidesUracilValine

Identifiers

PMID26895022
PMCPMC4933729

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Registered trials

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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.