Product Description
TIM-3 binding antibody (Sourced from: https://clinicaltrials.gov/ct2/show/NCT03680508)
Mechanisms of Action: TIM3 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: GSK
Company Location: BRENTFORD MIDDLESEX X0 TW8 9GS
Company CEO: Emma Walmsley
Additional Commercial Interests: None
Clinical Description

Countries in Clinic: Argentina, Australia, Belgium, Brazil, Canada, Czech Republic, Denmark, Finland, France, Germany, Greece, Italy, Japan, Korea, Mexico, Netherlands, Poland, Romania, Russia, Spain, Sweden, Taiwan, Thailand, Turkey, United Kingdom, United States
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Non-Small-Cell Lung Cancer
Phase 2: Cervical Cancer|Hodgkin Lymphoma|Liver Cancer|Melanoma|Uterine Cancer
Phase 1: Colorectal Cancer|Hepatocellular Carcinoma
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
219451 | P2 |
Recruiting |
Melanoma|Hodgkin Lymphoma |
2030-11-01 |
|
POPSTAR | P2 |
Recruiting |
Melanoma |
2029-10-05 |
|
NCT06238635 | P2 |
Recruiting |
Uterine Cancer|Cervical Cancer |
2026-02-01 |
|
jRCT2041230056 | P3 |
Not yet recruiting |
Non-Small-Cell Lung Cancer |
2026-01-31 |