In the letter, it is emphasized that by the end of 2025, a new drug for the treatment of delta hepatitis, bulvertid, was introduced in the country. However, the diagnosis and therapy of HDV are still conducted under a clinical protocol designed for hepatitis B.
ECAT members express concern that the lack of specific clinical recommendations and program documents for delta hepatitis diminishes the significance of this disease and complicates the acquisition of systemic funding and planning for patient assistance.
The appeal also cites data from the Republican Center for the Control of Hematogenous Viral Hepatitis and HIV, indicating that as of September 1, 2025, 17% of patients with hepatitis B (3,120 individuals) were found to have co-infection with delta hepatitis.
In this regard, ECAT representatives request the Ministry of Health to take two main steps:
- to create a working group involving representatives of the patient community to develop and implement a national program for delta hepatitis with separate funding,
- to develop and approve clinical recommendations for HDV as an independent nosology.
The image on the main page is illustrative: gemotest.ru.