Product Description
Mechanisms of Action: EGFR Antagonist
Novel Mechanism: No
Modality: Antibody
Route of Administration: Intravenous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Genmab
Company Location: 1253 COPENHAGEN K G7 00000
Company CEO:
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Squamous Cell Carcinoma|Head and Neck Cancer
Phase 2: Head and Neck Cancer|Squamous Cell Carcinoma|Colorectal Cancer|Non-Small-Cell Lung Cancer
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
2006-7041-83/hah | N/A |
Not yet recruiting |
Bone Cancer|Multiple Myeloma |
2021-09-01 |
|
DAHANCA 19 | P3 |
Completed |
Squamous Cell Carcinoma|Head and Neck Cancer |
2012-10-31 |
|
DAHANCA 19 | P3 |
Completed |
Squamous Cell Carcinoma|Head and Neck Cancer |
2012-07-01 |
|
Zalutumumab PK in SCCHN | P2 |
Terminated |
Squamous Cell Carcinoma|Head and Neck Cancer |
2012-06-15 |