ViiV Healthcare @ IAS 2017
ViiV Healthcare held a webinar to discuss abstracts presented at the IAS 2017 conference in Paris.
Dr. Michael Aboud and Dr. Jean Van Wyk from ViiV Healthcare will present a selection of Dolutegravir▼ (DTG) data.
Angelina Namiba, Project Manager at the Salamander Trust and member of the multi-disciplinary Steering Committee of the Positive Perspectives Study, will share the results of this international patient survey.
Chapter 1: Introduction & DAWNING Study
Presented by Dr. Michael Aboud, Vice President and Global Medical Lead, ViiV Healthcare.
Chapter 2: NEAT022 Study
Presented by Dr. Jean Van Wyk, Global Medical Affairs Director, ViiV Healthcare
Chapter 3: OPERA® Women’s analysis
Presented by Dr. Jean Van Wyk, Global Medical Affairs Director, ViiV Healthcare
Chapter 4: Positive Perspectives Survey Results & Insights
Presented by Angelina Namiba, Salamander Trust, UK
TRIUMEQ ▼ is indicated for the treatment of HIV-infected adults and adolescents above 12 years of age weighing at least 40kg.
Before initiating treatment with abacavir-containing products, HLA-B*5701 status must always be documented. Abacavir should not be used in patients known to carry the HLA-B*5701 allele due to the risk of hypersensitivity reaction.
TIVICAY ▼ is indicated in combination with other antiretroviral medicinal products for the treatment of HIV-infected adults, adolescents and children aged 6 years and over, weighing at least 15kg.
References:
- Aboud et al. IAS 2017; Paris, France. Slides TUAB0105LB.
- Gatell et al. NeatID. Slides. NEAT22/SSAT060 week 48 data
- Carpio et al. IAS Poster. Paris. WEPEB0573.
- Murungi A et al. IAS Poster. Paris WEPED1423.
Adverse events should be reported directly to the HPRA; Freepost, Pharmacovigilance Section, Health Products Regulatory Authority, Earlsfort Terrace, Dublin 2, Tel: +353 1 676 4971 medsafety@hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255.
▼ These medicinal products are subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.
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