Eligibility for Vemlidy depends on your diagnosis, disease activity, and individual health needs. Vemlidy is approved for adults and certain pediatric patients with chronic hepatitis B who need long-term antiviral therapy — for example, those with a durable need for viral suppression, evidence of liver disease progression, or a preference for a treatment option with an improved kidney and bone safety profile.
Clinical guidelines generally recommend starting antiviral treatment for chronic hepatitis B when HBV DNA levels are above 2,000 IU/mL, ALT is above the upper limit of normal, and there is at least moderate liver inflammation or fibrosis on biopsy or non-invasive testing. People with HBV DNA above 20,000 IU/mL and ALT more than twice the upper limit of normal are generally treated regardless of fibrosis stage. Tenofovir alafenamide is one of three nucleos(t)ide analogues generally preferred for first-line treatment, along with entecavir and tenofovir disoproxil fumarate.
Because every patient's health profile is different, there is no one-size-fits-all answer to who should take Vemlidy. Treatment decisions are individualized and should be made by a qualified healthcare professional after a full assessment of your liver condition, viral load, and treatment goals.