Efficacy and Safety of Long-Acting Subcutaneous Lenacapavir in Heavily Treatment-Experienced People with Multidrug-Resistant HIV-1: Week 104 Results of a Phase 2/3 Trial.

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Tác giả: Jason Brunetta, Francesco Castelli, Ploenchan Chetchotisakd, Gordon E Crofoot, Hadas Dvory-Sobol, Chien-Ching Hung, Nicolas A Margot, Jean-Michel Molina, Onyema Ogbuagu, Moti N Ramgopal, Martin S Rhee, Sylvie Ronot-Bregigeon, William Sanchez, Sorana Segal-Maurer, Hui Wang

Ngôn ngữ: eng

Ký hiệu phân loại: 629.13334 Aerospace engineering

Thông tin xuất bản: United States : Clinical infectious diseases : an official publication of the Infectious Diseases Society of America , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 715347

 BACKGROUND: Lenacapavir is a long-acting human immunodeficiency virus type 1 (HIV-1) capsid inhibitor for treatment of HIV-1 infection. We evaluated the efficacy and safety of lenacapavir in combination with an investigator-selected optimized background regimen (OBR) after 104 weeks in adults with multidrug-resistant HIV-1. METHODS: This ongoing, international, Phase 2/3 trial at 42 sites included 72 adults with multidrug-resistant HIV-1. Following a 2-week oral lenacapavir loading phase, participants received subcutaneous lenacapavir every 26 weeks with an OBR. HIV-1 RNA, CD4 cell counts, and adverse events were assessed over 104 weeks. One participant did not enter the extension phase. RESULTS: At Week 104, 44 of 71 participants (62%, 95% confidence interval [CI]: 50
  73) had HIV-1 RNA <
 50 copies/mL via US Food and Drug Administration (FDA) snapshot algorithm. When missing data (including discontinuations) were excluded, 44 of 54 participants (82%) had HIV-1 RNA <
 50 copies/mL at Week 104, mean CD4 cell count increased by 122 cells/µL (95% CI: 80
  165), and the proportion of participants with CD4 cell count <
 200 cells/µL decreased from 64% (46 of 72) at Baseline to 29% (16 of 55). Fourteen participants had treatment-emergent lenacapavir resistance
  7 resuppressed (HIV-1 RNA <
 50 copies/mL) while maintaining lenacapavir use. There were no Grade 4 or serious treatment-related adverse events. One participant discontinued study drug due to an injection site reaction. CONCLUSIONS: Treatment with subcutaneous lenacapavir in combination with an OBR was well tolerated and resulted in a high rate of virological suppression over 104 weeks. Lenacapavir represents an important treatment option in people with multidrug-resistant HIV-1.
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