Evidence map›Paper›PMID 31548188›Full record

ArticleAntimicrobial agents and chemotherapy2019

Doravirine exposure and HIV-1 suppression after switching from an efavirenz-based regimen to doravirine/lamivudine/tenofovir disoproxil fumarate.

Wayne Greaves, Hong Wan, Ka Lai Yee, Bhargava Kandala, Pavan Vaddady, Carey Hwang

Open access · hybridAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

6 authors at 2 institutions in 1 country.

Wayne GreavesGlobal Clinical Development Infectious Diseases, Merck & Co., Inc., Kenilworth NJ, USA wayne.greaves@merck.com.
Hong WanBiostatistics and Research Decision Sciences, Merck & Co., Inc., Kenilworth NJ, USA.
Ka Lai YeePharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck & Co., Inc., Kenilworth NJ, USA.
Bhargava KandalaPharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck & Co., Inc., Kenilworth NJ, USA.
Pavan VaddadyPharmacokinetics, Pharmacodynamics and Drug Metabolism, Merck & Co., Inc., Kenilworth NJ, USA.
Carey HwangGlobal Clinical Development Infectious Diseases, Merck & Co., Inc., Kenilworth NJ, USA.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USDecision Sciences (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Doravirine is a non-nucleoside reverse transcriptase inhibitor approved for the treatment of HIV-1. In a phase 1 trial, doravirine exposure was transiently decreased when treatment was started immediately after stopping efavirenz. In a post-hoc subgroup analysis of participants who switched from an efavirenz-based regimen to doravirine/lamivudine/tenofovir disoproxil fumarate in the phase 3 DRIVE-SHIFT trial, doravirine plasma levels at week 4 were similar to non-induced levels, and HIV-1 suppression was maintained at weeks 24 and 48.

Identifiers

PMID31548188
PMCPMC6879224
OpenAlexW2976414912

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.