Product Description
Mechanisms of Action: LOXL2 Antagonist
Novel Mechanism: Yes
Modality: Antibody
Route of Administration: Intravenous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Gilead Sciences
Company Location: FOSTER CITY CA 94404
Company CEO: Daniel P. O’Day
Additonal Commercial Interests: None
Clinical Description

Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 2: Liver Cirrhosis|Non-alcoholic Steatohepatitis|Liver Cirrhosis, Alcoholic|Fatty Liver, Alcoholic|Cholangitis, Sclerosing|Idiopathic Pulmonary Fibrosis|Idiopathic Interstitial Pneumonias|Pancreatic Cancer|Adenocarcinoma|Hepatitis, Alcoholic|Hepatitis C|Hepatitis A|Coinfection|Colorectal Cancer|Myelofibrosis|Thrombocytosis|Thrombocythemia, Essential|Polycythemia Vera
Phase 1: Idiopathic Pulmonary Fibrosis|Idiopathic Interstitial Pneumonias|Anal Cancer
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
2012-002489-11 | P2 |
Terminated |
Non-alcoholic Steatohepatitis|Hepatitis, Alcoholic|Liver Cirrhosis |
2019-01-26 |
|
2012-002488-88 | P2 |
Completed |
Hepatitis, Alcoholic|Liver Cirrhosis|Non-alcoholic Steatohepatitis |
2016-12-29 |
|
NASH | P2 |
Terminated |
Non-alcoholic Steatohepatitis|Liver Cirrhosis |
2016-09-26 |
|
2012-002473-61 | P2 |
Completed |
Cholangitis, Sclerosing |
2016-08-24 |