Product Description
or the treatment of chronic hepatitis B (HBV) infection. (Sourced from: https://www.sec.gov/Archives/edgar/data/1301081/000119312509084603/dex991.htm)
Mechanisms of Action: Viral Replication Inhibitor,DNA Synthesis Inhibitor
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: Korea | Philippines | Thailand
Approved Indications: None
Known Adverse Events: None
Company: Bukwang
Company Location:
Company CEO:
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 4: Hepatitis B|Hepatitis B, Chronic|Hepatitis A|Hepatocellular Carcinoma
Phase 3: Hepatitis B, Chronic|Hepatitis B|Hepatitis A|Other|Hepatitis D, Chronic
Phase 2: COVID-19|Hepatitis B|Hepatitis A|Hepatitis B, Chronic
Phase 1: Healthy Volunteers
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
1B-11-9 | N/A |
Terminated |
Breast Cancer |
2022-11-01 |
|
BK-CLV-203 | P2 |
Completed |
COVID-19 |
2021-07-05 |
25% |
BK-CLV-201 | P2 |
Completed |
COVID-19 |
2021-02-24 |
25% |
CLV-408 | P4 |
Terminated |
Hepatitis A|Hepatitis B, Chronic |
2014-11-01 |