Evidence map›Paper›PMID 33929078›Full record

ArticlePharmacology research & perspectives2021

Clinically relevant enantiomer specific R- and S-praziquantel pharmacokinetic drug-drug interactions with efavirenz and ritonavir.

Chenai Sheilla Mutiti, Nyasha Nicole Kapungu, Comfort Ropafadzo Kanji, Nadina Stadler, Julia Stingl, Charles Nhachi, James Hakim, Collen Masimirembwa, Roslyn Stella Thelingwani

Open access · goldAbstract readClinical Study
In one paragraph

Article in Pharmacology research & perspectives, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. 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 at 4 institutions in 2 countries.

Chenai Sheilla MutitiDepartment of Pharmaceutical Medicine, African Institute of Biomedical Science and Technology Block C Wilkins Hospital, Harare, Zimbabwe.
Nyasha Nicole KapunguDepartment of Pharmaceutical Medicine, African Institute of Biomedical Science and Technology Block C Wilkins Hospital, Harare, Zimbabwe.ORCID 0000-0002-3252-8753
Comfort Ropafadzo KanjiDepartment of Pharmaceutical Medicine, African Institute of Biomedical Science and Technology Block C Wilkins Hospital, Harare, Zimbabwe.ORCID 0000-0002-5278-0614
Nadina StadlerResearch Division Federal Institute for Drugs and Medical Devices, Bonn, Germany.
Julia StinglInstitute of Pharmacology and Toxicology, RWTG Aachen University Hospital, Aachen, Germany.
Charles NhachiClinical Pharmacology Department, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe.
James HakimDepartment of Medicine, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe.
Collen MasimirembwaDepartment of Pharmaceutical Medicine, African Institute of Biomedical Science and Technology Block C Wilkins Hospital, Harare, Zimbabwe.ORCID 0000-0002-4053-212X
Roslyn Stella ThelingwaniDepartment of Pharmaceutical Medicine, African Institute of Biomedical Science and Technology Block C Wilkins Hospital, Harare, Zimbabwe.ORCID 0000-0001-8396-6609
University of Zimbabwe · ZWAfrican Institute of Biomedical Science and Technology · ZWFederal Institute for Drugs and Medical Devices · DEUniversitätsklinikum Aachen · DE

Funding

Research Mentoring and Building Capacity of underrepresented Minority Research Scientists in India.D43TW010540 · FIC · YALE UNIVERSITY · PI MICHELE BARRY, Eva Harris · 2017 to 2026
$15.5M
FIC NIH HHS D43 TW010540
6 · The paper itself

Abstract

We conducted a clinical study to determine the effect of efavirenz and ritonavir on the pharmacokinetics of R- and S-PZQ in healthy male participants. This was toward evaluating the risk of drug-drug interactions, which may occur after PZQ administration to HIV patients on efavirenz or ritonavir containing regimens. A non-randomized, open-label, single-dose, one sequence crossover study with 2 arms was conducted. We gave 26 healthy volunteers a single oral dose of 40 mg/kg PZQ followed by a daily oral dose of either 400 mg efavirenz or 100 mg ritonavir for 14 consecutive days. On day 14, they ingested a single 40 mg/kg dose of PZQ. We measured plasma levels up to 12 h on day 1 and day 14. Samples were analyzed by LC-MS. Pharmacokinetic analysis was conducted in WinNonlin to determine the primary endpoints (plasma T

Indexed as

AdultAlkynesAnthelminticsAnti-HIV AgentsBenzoxazinesCross-Over StudiesCyclopropanesDrug InteractionsHumansMalePraziquantelRitonavirStereoisomerismYoung AdultAlkynesAnthelminticsAnti-HIV AgentsBenzoxazinesCyclopropanesefavirenzPraziquantelRitonavirdrug-drug interactionenantiomer specificpharmacokineticspraziquantel

Identifiers

PMID33929078
PMCPMC8085964
OpenAlexW3158085162

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.