- |||||||||| Cabenuva (cabotegravir long acting/rilpivirine long acting) / J&J, GSK, ViiV Healthcare, Pfizer, Shionogi
Safety of cabotegravir/rilpivirine long acting for individuals previously exposed to HBV infection (ePosters) - Oct 8, 2023 - Abstract #EACS2023EACS_568; Linear regression analysis failed to predict a significant FIB-4 evolution over time within the overall (b=-0.004, CI: -0.183-0.175, p=0.967), the HBV-exposed (b=-0.081, 95% CI: -0.440-0.279, p=0.659), and the unexposed population (b=-0.000, 95% CI: -0.180-0.180, p=0.997) (Figure 2). Conclusions :
- |||||||||| Cabenuva (cabotegravir long acting/rilpivirine long acting) / J&J, GSK, ViiV Healthcare, Pfizer, Shionogi
Safety of cabotegravir/rilpivirine long acting for individuals previously exposed to HBV infection (ePosters) - Oct 8, 2023 - Abstract #EACS2023EACS_567; Linear regression analysis failed to predict a significant FIB-4 evolution over time within the overall (b=-0.004, CI: -0.183-0.175, p=0.967), the HBV-exposed (b=-0.081, 95% CI: -0.440-0.279, p=0.659), and the unexposed population (b=-0.000, 95% CI: -0.180-0.180, p=0.997) (Figure 2). Conclusions :
- |||||||||| Cabenuva (cabotegravir long acting/rilpivirine long acting) / J&J, GSK, ViiV Healthcare, Pfizer, Shionogi
Trial completion date, Trial primary completion date: Implementing Cabenuva in Arkansas HIV Programs (clinicaltrials.gov) - Sep 13, 2023 P=N/A, N=100, Recruiting, iCAB/RPV may be considered as an option for patients unable to maintain suppression on oral antiretroviral therapy. Trial completion date: Dec 2023 --> Oct 2024 | Trial primary completion date: Dec 2023 --> Oct 2024
- |||||||||| Vocabria (cabotegravir oral) / ViiV Healthcare, Rekambys (rilpivirine LA) / J&J, Cabenuva (cabotegravir long acting/rilpivirine long acting) / J&J, GSK, ViiV Healthcare, Pfizer, Shionogi
Cabotegravir-rilpivirine long acting: data in real life setting in a large French cohort (ePosters area) - Sep 10, 2023 - Abstract #EACS2023EACS_263; Treatment interruption for VR was rare (0.5%) and analysis of emerging resistance at VR is ongoing. A prolonged follow-up is needed to confirm long term efficacy and tolerability.
- |||||||||| Cabenuva (cabotegravir long acting/rilpivirine long acting) / J&J, GSK, ViiV Healthcare, Pfizer, Shionogi
Trial initiation date: Study of Oral and Long-Acting Injectable Cabotegravir and Rilpivirine in Virologically Suppressed Children Living With HIV-1, Two to Less Than 12 Years of Age (clinicaltrials.gov) - Aug 16, 2023 P1/2, N=90, Not yet recruiting, Since individuals with the E138A mutation may be more likely to fail cabotegravir/rilpivirine, monitoring RPV-RAMs will be crucial for effective cabotegravir/rilpivirine implementation in this setting. Initiation date: Jul 2023 --> Oct 2023
- |||||||||| Edurant (rilpivirine) / J&J, Sublocade (buprenorphine once-monthly depot) / Indivior, Cabenuva (cabotegravir long acting/rilpivirine long acting) / J&J, GSK, ViiV Healthcare, Pfizer, Shionogi
New P1 trial, Adherence: CHOICE: Combined Injectable Treatment for HIV and OUD (clinicaltrials.gov) - Aug 14, 2023 P1, N=40, Recruiting,
- |||||||||| Vocabria (cabotegravir oral) / ViiV Healthcare, Rekambys (rilpivirine LA) / J&J, Cabenuva (cabotegravir long acting/rilpivirine long acting) / J&J, GSK, ViiV Healthcare, Pfizer, Shionogi
Journal, HEOR, Cost-effectiveness, Cost effectiveness: Cabotegravir and Rilpivirine Long-Acting Antiretroviral Therapy Administered Every 2 (Pubmed Central) - Jul 15, 2023 P3 A special focus on addressing the barriers of adherence and the cost of implementation is needed. From the Spanish National Health System perspective, CAB+RPV LA Q2M is a cost-effective alternative compared with the current options of daily oral STR regimens for HIV treatment.
- |||||||||| Vocabria (cabotegravir oral) / ViiV Healthcare, Cabenuva (cabotegravir long acting/rilpivirine long acting) / J&J, GSK, ViiV Healthcare, Pfizer, Shionogi
Journal: Demonstration Project of Long-Acting Antiretroviral Therapy in a Diverse Population of People With HIV. (Pubmed Central) - Jul 3, 2023 Further data on the ability of LA-ART to achieve viral suppression in people with barriers to adherence are needed. National Institutes of Health, City and County of San Francisco, and Health Resources and Services Administration.
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