Product Description
Mechanisms of Action: Unknown
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Intravenous
FDA Designation: Fast Track - Transitional Cell CarcinomaOrphan Drug - Pancreatic CancerOrphan Drug - Transitional Cell Carcinoma *
Approval Status: Not Approved
Approved Countries: Austria | Belgium | Croatia | Czech | Estonia | European Medicines Agency | Finland | Germany | Hungary | Iceland | Ireland | Israel | Italy | Latvia | Lithuania | Mexico | Poland | Portugal | Slovakia | Sweden
Approved Indications: None
Known Adverse Events: None
Company: Steba Biotech
Company Location:
Company CEO:
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic: Austria, France, Germany, Israel, Italy, Spain, United States
Active Clinical Trial Count: 7
Highest Development Phases
Phase 3: Bladder Cancer|Kidney Cancer|Kidney Diseases|Transitional Cell Carcinoma|Ureteral Cancer|Vascular Cancer
Phase 2: Prostate Cancer
Phase 1: Adenocarcinoma|Deglutition Disorders|Gastrointestinal Cancer|Lung Cancer|Nose Cancer|Pancreatic Cancer
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
CLIN2001UCM301 | P3 |
Unknown Status |
Transitional Cell Carcinoma |
2028-08-01 |
|
ENdoluminal LIGHT ActivatED Treatment of Upper Tract Urothelial Cancer (ENLIGHTED) Study | P3 |
Active, not recruiting |
Transitional Cell Carcinoma |
2028-05-11 |
|
CLIN2201 LCM101 | P1 |
Recruiting |
Nose Cancer|Vascular Cancer|Lung Cancer |
2027-05-30 |
|
CLIN2301 PNCM101 | P1 |
Recruiting |
Pancreatic Cancer|Adenocarcinoma |
2026-05-30 |