# Factors Associated With Weight Change After Continuing or Switching to a Doravirine-based Regimen

**Authors:** Chloe Orkin, John R Koethe, Princy N Kumar, Peter Sklar, Zhi Jin Xu, Rebeca M Plank, Wayne Greaves, Rima Lahoulou

PMC · DOI: 10.1093/ofid/ofaf639 · 2025-11-20

## TL;DR

This study found that switching to a doravirine-based HIV treatment generally does not cause significant weight changes, though some groups may experience different effects.

## Contribution

The study identifies demographic and prior regimen factors influencing weight changes when switching to doravirine-based HIV treatment.

## Key findings

- Most participants had stable weight after switching to doravirine-based regimens.
- Non-Black participants were more likely to experience weight loss or stable weight after switching.
- Switching from non-nucleoside reverse transcriptase inhibitors was linked to more weight gain.

## Abstract

Factors associated with weight change were examined in phase 3 studies in which adults living with HIV-1 continued or switched to doravirine-based antiretroviral regimens.

Participants were randomized to first-line therapy with doravirine or darunavir/ritonavir, each given with 2 nucleos(t)ide reverse transcriptase inhibitors (NRTIs) (DRIVE-FORWARD) and to doravirine/lamivudine/tenofovir disoproxil fumarate (TDF) or efavirenz/emtricitabine/TDF (DRIVE-AHEAD); after 96 weeks, participants continued (n = 466) or switched to (n = 423) doravirine for 96-week open-label extensions. In DRIVE-SHIFT, virologically suppressed participants on stable antiretroviral therapy were randomized to switch to doravirine/lamivudine/TDF at day 1 or week 24 through week 144 (n = 535). Generalized logistic models were used to analyze factors associated with weight loss (≥5% decrease), stable weight (<5% change), and weight gain (≥5% increase) after continuation or switch.

Most participants who continued or switched to doravirine also received TDF (>74%) and had stable weight (>57%). Weight loss (odds ratio [OR], 6.14) or stable weight (OR, 2.15) was more common in participants of non-Black versus Black heritage after switching to doravirine. More participants switching from weight-suppressive non-nucleoside reverse transcriptase inhibitors versus protease inhibitors experienced weight gain versus weight loss in DRIVE-SHIFT (OR, 0.41) and weight gain versus stable weight in DRIVE-FORWARD and DRIVE-AHEAD (OR, 0.60). No significant association between weight change and prior NRTI use was observed in DRIVE-SHIFT.

Overall, switching to doravirine was weight neutral, although weight change may differ by demographics and weight-suppressive properties of a prior regimen. More research in historically underrepresented groups may help explain these findings.

NCT02275780, NCT02403674, NCT02397096.

In three phase 3 clinical studies, switching to a doravirine-based regimen was weight neutral in most adults with HIV-1, although weight change differed across demographic subgroups and according to weight-suppressive properties of a prior regimen.

## Linked entities

- **Chemicals:** doravirine (PubChem CID 58460047), darunavir/ritonavir (PubChem CID 42636391), lamivudine (PubChem CID 60825), tenofovir disoproxil fumarate (PubChem CID 5486830), efavirenz (PubChem CID 3203), emtricitabine (PubChem CID 60877)

## Full-text entities

- **Diseases:** Weight (MESH:D015431), weight gain (MESH:D015430)
- **Chemicals:** Doravirine (MESH:C000592662), lamivudine (MESH:D019259), tenofovir disoproxil fumarate (MESH:D000068698), efavirenz (MESH:C098320), NRTI (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12631767/full.md

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Source: https://tomesphere.com/paper/PMC12631767