IDDF2024-ABS-0269 Results from an integrated analysis at week 96: continued treatment of early virologic non-responder or partial responders with bulevirtide monotherapy for chronic hepatitis d leads to improvement in virologic and biochemical respon

<h3>Background</h3> Bulevirtide (BLV) is approved in Europe for the treatment of chronic hepatitis D (CHD). Optimal BLV monotherapy duration for CHD is unknown). This analysis evaluated BLV monotherapy in pts without VR after 24W. <h3>Methods</h3> Results from pts who completed BLV monotherapy for 96W in the Phase 3 (MYR301) and Phase 2 (MYR204) studies were included. NR and PR were defined as HDV RNA declines of &lt;1 log10 IU/mL and ≥1 but &lt;2 log10 IU/mL, respectively. Rates of biochemical response (alanine aminotransferase [ALT] within normal limits [WNL]) were compared. <h3>Results</h3> At W24, 65% pts had VR (58% with ALT WNL), 24% had PR (56% with ALT WNL), and 11% had NR (13% with ALT WNL) (IDDF2024-ABS-0269 Table 1). <h3>Conclusions</h3> Of 49 pts without VR at W24, the majority with PR and nearly half with NR were able to achieve VR at W96. ALT improved in all viral-response groups, including those with NR.

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Published
2024-08-01
DOI
https://doi.org/10.1136/gutjnl-2024-iddf.194
Primary Topic
Hepatitis C virus research
Type
article
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IDDF2024-ABS-0269 Results from an integrated analysis at week 96: continued treatment of early virologic non-responder or partial responders with bulevirtide monotherapy for chronic hepatitis d leads to improvement in virologic and biochemical respon

Markus Cornberg, Anu Osinusi, Dmitry Manuilov, Tarik Asselah et al.
Hepatitis C virus research
article

IDDF2024-ABS-0269 Results from an integrated analysis at week 96: continued treatment of early virologic non-responder or partial responders with bulevirtide monotherapy for chronic hepatitis d leads to improvement in virologic and biochemical respon

Markus Cornberg, Anu Osinusi, Dmitry Manuilov, Tarik Asselah, Mark Bourliere, Pavel Bogomolov, Renée-Claude Mercier, Tatyana Stepanova, Soo Aleman, Stefan Zeuzem, Dominique Roulot, John F. Flaherty, Fabien Zoulim, H. Fontaine, Carrie Frenette, Heiner H. Wedemeyer, Grace M. Chee, Maurizia Rossana Brunetto, George Sebastian Gherlan, Audrey Lau, Ben L. Da, Qi An, Pietro Lampertico, Jacques Yu, Adrian Streinu-Cercel
article en

Abstract

<h3>Background</h3> Bulevirtide (BLV) is approved in Europe for the treatment of chronic hepatitis D (CHD). Optimal BLV monotherapy duration for CHD is unknown). This analysis evaluated BLV monotherapy in pts without VR after 24W. <h3>Methods</h3> Results from pts who completed BLV monotherapy for 96W in the Phase 3 (MYR301) and Phase 2 (MYR204) studies were included. NR and PR were defined as HDV RNA declines of &lt;1 log10 IU/mL and ≥1 but &lt;2 log10 IU/mL, respectively. Rates of biochemical response (alanine aminotransferase [ALT] within normal limits [WNL]) were compared. <h3>Results</h3> At W24, 65% pts had VR (58% with ALT WNL), 24% had PR (56% with ALT WNL), and 11% had NR (13% with ALT WNL) (IDDF2024-ABS-0269 Table 1). <h3>Conclusions</h3> Of 49 pts without VR at W24, the majority with PR and nearly half with NR were able to achieve VR at W96. ALT improved in all viral-response groups, including those with NR.

Goethe University Frankfurt (DE), Karolinska University Hospital (SE), Carol Davila University of Medicine and Pharmacy (RO), University of Milan (IT), Université Paris Cité (FR), Hôpital Beaujon (FR), Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico (IT), Karolinska Institutet (SE), Medizinische Hochschule Hannover (DE), Sorbonne Université (FR), Hôpital de la Croix-Rousse (FR), Université Sorbonne Paris Nord (FR), Institutul National Victor Babes (RO), Hôpital Saint Joseph (FR), Moscow Institute of Modern Business (RU), University Hospital Frankfurt (DE), Gilead Sciences (United States) (US), Azienda Ospedaliera Universitaria Pisana (IT)
Good health and well-being
Openalex Percentile: Top 78%
Hepatitis C virus research
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