-
ViiV-Sponsored Data
Cabotegravir Prevention
Baker DM, et al.
Change in Healthcare Professional’s Identification, Counseling, and Adherence with Black Women for Long-Acting Cabotegravir (CAB LA) for PrEP Across Women’s Health, Primary Care, and Infectious Diseases Sites: Findings from the EBONI StudyView
×Baker DM, et al.
Change in Healthcare Professional’s Identification, Counseling, and Adherence with Black Women for Long-Acting Cabotegravir (CAB LA) for PrEP Across Women’s Health, Primary Care, and Infectious Diseases Sites: Findings from the EBONI StudyCollapse ❯ Expand ❮- Full Poster
- Title
- Key Takeaways
- Introduction
- Methods
- Results
- Figure 1. HCP Perceptions of CAB LA of Appropriateness and Feasibility
- Figure 2. HCP Perceptions of CAB LA
- Figure 3. Factors Related to Patient Identification, Counseling, and Adherence
- Figure 4. HCP Strategies for Supporting CAB LA Patient Adherence
- Figure 5. Usefulness of Provider Support Tools
- Conclusions
- Disclaimer
Holder H, et al.
Patient Experiences at Month 6 after Initiation of Cabotegravir Long-Acting (CAB LA) for PrEP in the First Male Gender Concordant Implementation Science Trial (PILLAR) in the USView
×Holder H, et al.
Patient Experiences at Month 6 after Initiation of Cabotegravir Long-Acting (CAB LA) for PrEP in the First Male Gender Concordant Implementation Science Trial (PILLAR) in the US×Collapse ❯ Expand ❮- Full Poster
- Title
- Background
- Methods
- Results
- Figure 1. Self-reported PrEP knowledge, effectiveness, and importance
- Figure 2. Conversations about PrEP
- Figure 3. Among prescribers, likelihood of prescribing PrEP and LA PrEP
- Figure 4. Importance of various patient factors for recommending PrEP
- Figure 5. Among prescribers, likelihood of prescribing LA PrEP to various individuals, by patient and sexual partner(s)
- Figure 6. Among prescribers, likelihood of prescribing LA PrEP to various individuals, by patient and characteristic
- Discussion
- Key Findings
- Acknowledgments
- Disclaimer
Kerrigan D, et al.
Social Determinants of Health and Side Effects Significantly Predict Pre-Exposure Prophylaxis (PrEP) Preferences for Every 2 Month Long-Acting Injectable vs. Daily Oral PrEP among Cisgender Women in the United States and the Dominican RepublicView
×Kerrigan D, et al.
Social Determinants of Health and Side Effects Significantly Predict Pre-Exposure Prophylaxis (PrEP) Preferences for Every 2 Month Long-Acting Injectable vs. Daily Oral PrEP among Cisgender Women in the United States and the Dominican RepublicKhan TH, et al.
Improvement in Provider Experiences from Baseline to Month 12 with Integrating Cabotegravir Long-Acting (CAB LA) for PrEP into Care in an Implementation Science Trial (PILLAR)View
×Khan TH, et al.
Improvement in Provider Experiences from Baseline to Month 12 with Integrating Cabotegravir Long-Acting (CAB LA) for PrEP into Care in an Implementation Science Trial (PILLAR)Metzner AA, et al.
Awareness and preferences for every 2 month long-acting injectable HIV Pre-Exposure Prophylaxis (PrEP) versus daily oral PrEP among cisgender women in the United States and the Dominican RepublicView
×Metzner AA, et al.
Awareness and preferences for every 2 month long-acting injectable HIV Pre-Exposure Prophylaxis (PrEP) versus daily oral PrEP among cisgender women in the United States and the Dominican RepublicMills A, et al.
Cabotegravir Long-Acting for Pre-Exposure Prophylaxis (PrEP): Real World Data on On-Time Dosing, HIV Testing and HIV Acquisition from the OPERA CohortView
×Mills A, et al.
Cabotegravir Long-Acting for Pre-Exposure Prophylaxis (PrEP): Real World Data on On-Time Dosing, HIV Testing and HIV Acquisition from the OPERA CohortCollapse ❯ Expand ❮- Title
- Disclosures
- Background & Objectives
- Pre-exposure prophylaxis (PrEP) landscape
- Cabotegravir long-acting (CAB LA) PrEP dosing schedule
- Objectives and Methods
- Study objectives
- OPERA The Longitudinal Cohort
- Study population
- Results
- Baseline characteristics of CAB LA PrEP and oral PrEP users (1)
- Baseline characteristics of CAB LA PrEP and oral PrEP users (2)
- Complete vs. incomplete initiation among all CAB LA PrEP users
- Complete vs. incomplete initiation among all CAB LA PrEP users (continued)
- On-time injections among complete initiators
- On-time injections among complete initiators (continued)
- Delayed injections among complete initiators
- Delayed injections among complete initiators (continued)
- Missed continuation injections among complete initiators
- Missed continuation injections among complete initiators (continued)
- HIV testing within 1 week before/at 1st CAB LA PrEP injection
- HIV testing within 1 week before/at subsequent CAB LA PrEP injection
- HIV acquisition among CAB LA PrEP users
- Case #1
- Case #2
- Discussion
- Key findings (1)
- Key findings (2)
- Strengths & limitations
- Acknowledgements
- Disclaimer
Poteat T, et al.
Opportunities for PrEP Awareness and Engagement: A Survey among Healthcare-Seeking Cisgender Women in the USView
×Poteat T, et al.
Opportunities for PrEP Awareness and Engagement: A Survey among Healthcare-Seeking Cisgender Women in the USRamgopal M, et al.
Real-World Use of Cabotegravir Long-Acting for Pre-Exposure Prophylaxis: Data from Trio Health CohortView
×Ramgopal M, et al.
Real-World Use of Cabotegravir Long-Acting for Pre-Exposure Prophylaxis: Data from Trio Health CohortCollapse ❯ Expand ❮- Title
- Disclosures
- Background
- Study Objectives
- Methods
- Study Design
- Study Outcomes
- Results - 2 Year Analysis
- Study Population
- Characteristics at Regimen Initiation
- HIV Risk Factors and Prior PrEP Use at Initiation
- Persistence
- Discontinuations
- On Time Injections
- HIV Screening and Seroconversion
- Safety
- Limitations
- Conclusions
- Thank You
- Disclaimer
Cabotegravir Treatment
Altamirano JA, et al.
Characteristics of Women Initiating CAB+RPV LA in the OPERA CohortView
×Collapse ❯ Expand ❮- Full Poster
- Title
- Background
- Methods
- Results
- Table 2. Clinical characteristics at initiation of CAB+RPV LA injections, stratified by baseline VL
- Table 3. ART history at initiation of CAB+RPV LA injections, stratified by baseline VL
- Figure 1. CAB+RPV LA dosing at initiation and at study end among complete initiators, stratified by baseline VL
- Discussion
- Key Findings
- Acknowledgements
- Disclaimer
Brogan AP, et al.
People with HIV in the US switching to cabotegravir + rilpivirine long-acting (CAB+RPV LA) from oral antiretroviral therapy (ART) have numerous real-world benefits, including high adherence and treatment satisfactionView
×Brogan AP, et al.
People with HIV in the US switching to cabotegravir + rilpivirine long-acting (CAB+RPV LA) from oral antiretroviral therapy (ART) have numerous real-world benefits, including high adherence and treatment satisfactionGutner CA, et al.
Feasibility, Fidelity, and Effectiveness of Administering CABENUVA in Infusion CentersView
×Gutner CA, et al.
Feasibility, Fidelity, and Effectiveness of Administering CABENUVA in Infusion CentersLackey PC, et al.
Improved Testing for Chronic Disease Among Long-Acting Injectable Versus Daily Oral Antiretroviral Therapy Users in the OPERA CohortView
×Lackey PC, et al.
Improved Testing for Chronic Disease Among Long-Acting Injectable Versus Daily Oral Antiretroviral Therapy Users in the OPERA CohortCollapse ❯ Expand ❮- Full Poster
- Title
- Background
- Methods
- Results
- Table 2. Calculations of risk score composites over follow-up, by ART group
- Figure 1. Proportions of PWH who received lipid testing over follow-up, by ART group
- Figure 2. Proportions of PWH who received serum glucose testing over follow-up, by ART group
- Discussion
- Key Findings
- Reference, Acknowledgements
- Disclaimer
Dolutegravir-based Regimens
Doblado-Maldonado A, et al.
Real-world Virologic and Safety Outcomes in People Living with HIV-1 Using Dolutegravir (DTG) + Lamivudine (3TC) in Asia Stratified by Viral Load (VL), Including in Individuals with High VLsView
×Doblado-Maldonado A, et al.
Real-world Virologic and Safety Outcomes in People Living with HIV-1 Using Dolutegravir (DTG) + Lamivudine (3TC) in Asia Stratified by Viral Load (VL), Including in Individuals with High VLsCollapse ❯ Expand ❮Huchet E, et al.
Real-world Experience with the Two-Drug Regimen Dolutegravir/Lamivudine for the Treatment of HIV-1 among Vulnerable People Living with HIV in Canada: Preliminary Results from a Chart Review StudyView
×Huchet E, et al.
Real-world Experience with the Two-Drug Regimen Dolutegravir/Lamivudine for the Treatment of HIV-1 among Vulnerable People Living with HIV in Canada: Preliminary Results from a Chart Review StudyJones CB, et al.
Evaluation of Weight Gain on Incident Hypertension among People Living with HIV-1 Receiving Dolutegravir (DTG)-Based Regimens or Comparator Antiretroviral Therapy (cART) in Randomized Clinical Trials through 96 WeeksView
×Jones CB, et al.
Evaluation of Weight Gain on Incident Hypertension among People Living with HIV-1 Receiving Dolutegravir (DTG)-Based Regimens or Comparator Antiretroviral Therapy (cART) in Randomized Clinical Trials through 96 WeeksShort WR, et al.
Extrapolating Expected Efficacy, Safety, and Pharmacokinetics (PK) of Dolutegravir/Lamivudine (DTG/3TC) in Pregnant People Living with HIV-1 from Pregnancy Data with Combination DTG and/or 3TC Antiretroviral TherapiesView
×Short WR, et al.
Extrapolating Expected Efficacy, Safety, and Pharmacokinetics (PK) of Dolutegravir/Lamivudine (DTG/3TC) in Pregnant People Living with HIV-1 from Pregnancy Data with Combination DTG and/or 3TC Antiretroviral TherapiesSlim J, et al.
PAIRED - PAtIent Reported Experiences and perceiveD benefit of treatment with dolutegravir/lamivudine (DTG/3TC): a diverse sample of people with HIV-1 reporting high treatment satisfaction, good adherence, and high quality of lifeView
×Slim J, et al.
PAIRED - PAtIent Reported Experiences and perceiveD benefit of treatment with dolutegravir/lamivudine (DTG/3TC): a diverse sample of people with HIV-1 reporting high treatment satisfaction, good adherence, and high quality of lifeFostemsavir
Castagna A, et al.
Similar Efficacy, Safety and CD4 T-cell Increase up to Week 96 Observed with Fostemsavir (FTR)-Based Regimens in the BRIGHTE Study and Dolutegravir (DTG)-Based Regimens in the VIKING-3 Study in Individuals with Multidrug-Resistant (MDR) HIV-1View
×Castagna A, et al.
Similar Efficacy, Safety and CD4 T-cell Increase up to Week 96 Observed with Fostemsavir (FTR)-Based Regimens in the BRIGHTE Study and Dolutegravir (DTG)-Based Regimens in the VIKING-3 Study in Individuals with Multidrug-Resistant (MDR) HIV-1Spagnuolo V, et al.
CD4 T-cell, CD4/CD8 Ratio Improvement and a General Reduction in Inflammatory Biomarkers with Low-Level Viremia (LLV) up to Week 192 with Fostemsavir (FTR)-Based Regimens in Individuals with Multidrug-Resistant (MDR) HIV-1View
×Spagnuolo V, et al.
CD4 T-cell, CD4/CD8 Ratio Improvement and a General Reduction in Inflammatory Biomarkers with Low-Level Viremia (LLV) up to Week 192 with Fostemsavir (FTR)-Based Regimens in Individuals with Multidrug-Resistant (MDR) HIV-1This content was acquired following an unsolicited medical information enquiry by a healthcare professional. Always consult the product information for your country, before prescribing a ViiV medicine. ViiV does not recommend the use of our medicines outside the terms of their license. In some cases, the scientific Information requested and downloaded may relate to the use of our medicine(s) outside of their license.
-
ViiV-Supported & Collaborative Data
This content was acquired following an unsolicited medical information enquiry by a healthcare professional. Always consult the product information for your country, before prescribing a ViiV medicine. ViiV does not recommend the use of our medicines outside the terms of their license. In some cases, the scientific Information requested and downloaded may relate to the use of our medicine(s) outside of their license.
-
Plain Language Summaries
View plain language summaries of select congress presentations. These summaries include non-technical language and are formatted to help make the information accessible to a wider audience.
Are you a US healthcare provider?
This web portal is intended as an educational resource for healthcare providers practicing in the United States. It may include information about products or uses that have not been approved by the US Food and Drug Administration.
If you are not a healthcare provider, please discuss any questions you have regarding your health or medicines with your doctor, pharmacist, or nurse.
Find My ViiV MSL
Easily find the ViiV Medical Science Liaison (MSL) in your area.
Request a Scientific Discussion
Submit a request for additional information from a ViiV Medical Expert.
Chat Live
Get immediate assistance from a ViiV Healthcare Professional.
Call 1‑888‑226‑8434
Weekdays from 8 AM to 6 PM ET
(5 AM – 3 PM PT)
Report an Adverse Event
To report SUSPECTED ADVERSE REACTIONS, contact ViiV Healthcare at 1‑877‑844‑8872 or FDA at 1‑800‑332‑1088 or www.fda.gov/medwatch