Evidence map›Paper›PMID 42418369›Full record

ArticlePloS one2026

A novel design using a virtual control group to evaluate non-inferiority of nevirapine and lamivudine dual maintenance in HIV therapy.

Alessandro Suter, Markus Bickel, Carsten Depmeier, Peter Gute, Gaby Knecht, Marcel Stöckle, Christoph Fux, Baharak Babouee Flury, Patrick Schmid, Pietro Vernazza and 1 more

Abstract readEquivalence TrialMulticenter Study
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Alessandro SuterDivision of Infectious Diseases and Infection Control, Health Ostschweiz (HOCH), Cantonal Hospital St. Gallen, St. Gallen, Switzerland.ORCID https://orcid.org/0009-0000-4891-6614
Markus BickelInfektiologikum Frankfurt, Frankfurt am Main, Germany.
Carsten DepmeierPrivate practice Wyssgasse, Zurich, Switzerland.
Peter GuteInfektiologikum Frankfurt, Frankfurt am Main, Germany.
Gaby KnechtInfektiologikum Frankfurt, Frankfurt am Main, Germany.
Marcel StöckleDivision of Infectious Diseases and Hospital Epidemiology, University Hospital of Basel, Basel, Switzerland.
Christoph FuxDivision of Infectious Diseases, Cantonal Hospital of Aarau, Aarau, Switzerland.
Baharak Babouee FluryDivision of Infectious Diseases and Infection Control, Health Ostschweiz (HOCH), Cantonal Hospital St. Gallen, St. Gallen, Switzerland.
Patrick SchmidDivision of Infectious Diseases and Infection Control, Health Ostschweiz (HOCH), Cantonal Hospital St. Gallen, St. Gallen, Switzerland.
Pietro VernazzaDivision of Infectious Diseases and Infection Control, Health Ostschweiz (HOCH), Cantonal Hospital St. Gallen, St. Gallen, Switzerland.
Christian R KahlertDivision of Infectious Diseases and Infection Control, Health Ostschweiz (HOCH), Cantonal Hospital St. Gallen, St. Gallen, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeReducing the number of drugs in combined antiretroviral therapy (cART) likely reduces toxicity. We hypothesized that dual therapy (DT) with nevirapine (NVP) and lamivudine (3TC) would be non-inferior to a virtual control without treatment failure.

methodsThis multicenter study enrolled patients on cART with HIV plasma viral load (pVL) <50 cp/ml for ≥2 years and on NVP for ≥6 months. Patients were compared to a simulated virtual control group with an assumed failure rate of zero. Those with prior Non-Nucleoside Reverse Transcriptase Inhibitor failure or 3TC resistance were excluded. Treatment was simplified to DT with NVP/3TC for 48 weeks, with quarterly pVL-measurements. The primary endpoint was confirmed virologic failure (pVL ≥ 200 cp/mL). A 4% non-inferiority margin and sample size of 201 were set, with a stopping rule if three virologic failures occurred.

resultsFrom April 2019 to January 2023, 201 patients from five centers in Switzerland and Germany started DT, which 194 participants completed. Two patients (1.03%, 95% CI: -0.92% to 3.68%) reached the primary endpoint for failure due to adherence issues. No additional failures were observed during a 12-month post-study follow-up of 184 participants.

conclusionsSimplification to NVP and 3TC was as effective as the ideal virtual control. However, the results of NVP and 3TC maintenance therapy are only applicable to people living with HIV who meet the study's inclusion and exclusion criteria. Virtual controls could improve research efficiency and warrant further evaluation.

Indexed as

Anti-HIV AgentsHIV InfectionsLamivudineNevirapineAdultDrug Therapy, CombinationFemaleHIV-1HumansMaleMiddle AgedViral LoadAnti-HIV AgentsLamivudineNevirapine

Identifiers

PMID42418369
PMCPMC13345260

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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.