Skip to content

HEPANTIVIR CLINICAL TRIAL

EVALUATION OF THE EFFICACY OF HEPANTIVIR (SECURININE) IN PATIENTS WITH CHRONIC HEPATITIS B INFECTION

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201507001055177
Enrollment
50
Registered
2015-03-05
Start date
2015-05-01
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HEPATITIS HEPATITIS

Interventions

None listed

Sponsors

BOLAR PHARMACEUTICALS LTD
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Fifty consecutive and consenting patients being managed by gastroenterology unitwith clinical and biochemical features as well as serological evidence of chronic hepatitis B infection and who meet the study criteria- 18 years and above, HBsAg positive with elevated serum ALT, Serum HBV DNA > 2000iu/ml

Exclusion criteria

Exclusion criteria: No consent, presence of underlying liver malignancy, presence of co-morbidities eg end-organ failure

Design outcomes

Primary

MeasureTime frame
improvement in symptoms, laboratory measurement including transaminase and HBV load as well as any adverse event will be compared between the treatment arm and tenofovir using chi sqaure test.

Secondary

MeasureTime frame
Absence of HBV DNA

Countries

Nigeria

Contacts

Public ContactBOLADE SOREMEKUN

SPONSOR

b.soremekun@bolarpharm.com+2348034499670

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026