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Pipeline
Company | Drug/Device | Medical Condition | Status |
---|---|---|---|
LB Pharmaceuticals | LB-102 | schizophrenia | phase 1 trial dosing initiated |
Stealth BioTherapeutics | SBT-272 | mitochondrial dysfunction | phase 1 trial initiated enrolling 60 patients |
Rafael Pharmaceuticals | CPI-613® (devimistat) in combination with gemcitabine and cisplatin | advanced, unresectable or metastatic biliary tract cancer | phase 1b/2 trial initiated |
BlackThorn Therapeutics | BTRX-335140 (BTRX-140) |
major depressive disorder | phase 2 trial initiated |
Aldeyra Therapeutics | reproxalap ophthalmic solution | allergic conjunctivitis | phase 3 trial enrolling 120 patients |
Wize Pharma | LO2A | dry eye syndrome in patients with Sjögren's syndrome | phase 4 trial enrollment completed with 60 patients |
Clovis Oncology | Rubraca (rucaparib) | metastatic castrate-resistant prostate cancer | Priority Review designation granted by the FDA |
Fortress Biotech | CUTX-101 | Menkes Disease | Rare Pediatric Disease designation granted by the FDA |
MedAlliance | Selution SLR drug-eluting balloon |
AV-fistula | Breakthrough Device designation granted by the FDA |
Ra Medical Systems | DABRA excimer laser system | peripheral vascular stenoses | IDE granted by the FDA |
INHIBITOR Therapeutics | SUBA-Itraconazole | metastatic castrate resistant prostate cancer | IND approved by the FDA |
Cadent Therapeutics | CAD-1883 Spinocerebellar Ataxia | spinocerebellar ataxia | IND approved by the FDA |
AstraZeneca | Imfinzi (durvalumab) and tremelimumab | hepatocellular carcinoma | Orphan Drug status granted by the FDA |
Baze | at-home blood test kit | blood nutrient levels | approved by the FDA |
Horizon Therapeutics | Tepezza (teprotumumab-trbw) | thyroid eye disease | approved by the FDA |
Medtronic | Micra AV pacemaker | atrioventricular block | approved by the FDA |
Merck | Keytruda (pembrolizumab) in combination with Inlyta (axitinib) | advanced renal cell carcinoma | approved by Health Canada |
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