Product Description
an oral FGFR1-3 inhibitor (Sourced from: https://ascopubs.org/doi/10.1200/JCO.19.02630)
Mechanisms of Action: FGFR Antagonist,TK Inhibitor
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: AstraZeneca
Company Location: CAMBRIDGE X0 CB2 0AA
Company CEO: Pascal Soriot
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic: China, United Kingdom
Active Clinical Trial Count: 3
Highest Development Phases
Phase 2: Adenocarcinoma|Non-Small-Cell Lung Cancer|Squamous Cell Carcinoma|Transitional Cell Carcinoma
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
ABSK091-203 | P2 |
Recruiting |
Transitional Cell Carcinoma |
2025-09-30 |
57% |
National Lung Matrix Trial | P2 |
Active, not recruiting |
Squamous Cell Carcinoma|Non-Small-Cell Lung Cancer|Adenocarcinoma |
2024-09-01 |
|
CTR20222326 | P2 |
Recruiting |
Transitional Cell Carcinoma |
None |