

The Treatment Action Group (TAG) was founded in January 1992 in New York City by former members of the ACT UP New York Treatment and Data Committee. It was established as an independent, non-profit organization to accelerate HIV/AIDS research, advocacy, and treatment, later expanding to include tuberculosis and hepatitis C.
TAG has been at the forefront of a global HCV education and advocacy movement, working in collaboration with affected communities, scientists, government, and pharmaceutical developers to make life-saving information, high quality and affordable testing and cures, and supportive environments for underserved populations universally available. This includes tracking the pipeline for HCV innovations, including the latest pangenotypic treatments, diagnostics, and long-acting injectables, and increasing communities’ diagnostics and treatment literacy. Globally, TAG provides technical assistance to build leadership capacity for advancing national elimination campaigns and amplifying community voices—especially those of key populations such as people who use and inject drugs, sex workers, prisoners, migrants, and men who have sex with men—in planning and policy development.
TAG aims to overcome barriers to access—from limited donor funding for HCV, to drug and alcohol abstinence requirements imposed by governments and payers, to patent and pricing barriers, to limited voluntary licensing and delays in drug registration by patent holders. TAG advocates for harm reduction and drug decriminalization efforts, including support for overdose prevention and safe consumption sites because injection drug use without access to safe materials is a major factor in HCV transmission.
In the U.S., TAG’s policy team works at the national level: advocating for viral hepatitis funding, championing coverage for people who use drugs, incarcerated or otherwise marginalized people, expanding access to point-of-care testing, strengthening national surveillance and supporting community engagement. TAG’s advocacy helped advance coverage for universal adult HCV screening and removal of Medicaid prior authorization requirements, catalyzing New York State’s commitment to eliminate HCV—the first in the nation! – with TAG participating in the resultant statewide HCV Elimination Task Force.
Hepatitis and PWID/harm reduction
11:35 – 11:40
Chair: WHO – Intro and set the scene.
11:40 – 11:55
Co-chair: EMCDDA – Monitoring viral hepatitis elimination among PWID in Europe.
11:55 – 12:00
ID 29: Ema Pos (not yet registered)
Title: If the mountain won’t come to Mohammed: lessons from a decentralized Infectious Disease consultation.
12:05 – 12:10
ID 152: Brian Conway (Registered in person)
Title: Community Pop-up Clinic: Cascade of Care and HCV Treatment of Vancouver’s inner-city PWID Populations.
12:10 – 12:15
ID 212: Jasmine West (not yet registered)
Title: From lived experience to lived expertise: a syndemic approach.
12:15 – 12:20
ID: 299 Mercy Nyakowa (Registered in person)
Title: HCV and HBV prevalence and associated risk factors among people who inject drugs (PWIDs) in Kenya
12:20 – 12:25
ID: 133 Nalinikanta Rajkumar (Registered in person)
Title: Rapid regimen of HBV vaccination: Does it work for high risk groups?
12:25 – 12:30
Q&A and closing remarks
tHIS
IS
BEN’S
BIG
TEST
effective case finding strategies
Supported by Vir Biotechnology, Inc
During this session you will hear from hepatitis Delta expert, Dr. Maria Buti, and a patient who has lived with hepatitis Delta in a panel discussion moderated by Dr. Carey Hwang, Chief Medical Officer (interim) of Vir Biotechnology. This panel will inform perspectives on patient needs, opportunities for enhanced screening, and strengthening linkages to care.
Session Agenda
14:40 – 14:45
Panel overview and introductions facilitated by Dr Carey Hwang (Vir Biotechnology)
14:45 – 15:05
Panel discussion: Dr Maria Buti (University Hospital Vall d’Hebron, Spain), Milanka Barbosa, Dr Carey Hwang (Chief Medical Officer interim), Vir Biotechnology
15:05 – 15:10
Final remarks and close