Pharmacoepidemiology study to define the long-term safety profile of tenofovir disoproxil fumarate (Tenofovir DF, Viread®) and describe the management of Tenofovir DF-associated renal and bone toxicity in Chronic Hepatitis B (CHB)-infected adolescents aged 12 to <18 years in Europe (Viread HBV PASS)

28/04/2017
01/04/2024
EU PAS number:
EUPAS18825
Study
Finalised
Documents
Study protocol
Initial protocol
English (928.43 KB - PDF) View document
Study results
Study results
English (296.29 KB - PDF) View document
Study report
Other information