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Pipeline
February 26, 2018
Company | Drug/Device | Medical Condition | Status |
---|---|---|---|
Arch Biopartners | AB569 | antibiotic-resistant bacterial infections in the lungs of cystic fibrosis and chronic obstructive pulmonary disease | Phase I trials initiated in the U.S. |
Xencor | XmAb18087 | neuroendocrine tumors (NET) and gastrointestinal stromal tumors (GIST) | Phase I trials initiated |
PQ Bypass | DETOUR | Long (>15 cm) superficial femoral artery (SFA) blockages | Phase I trials initiated enrolling 292 subjects in the U.S. and Europe |
Therachon | TA-46 | achondroplasia | Phase I trials initiated enrolling 70 subjects in the Netherlands |
OncoPep | PVX-4106 | metastatic triple negative breast cancer (TNBC) who are human leukocyte antigen A2 positive (HLA-A2+) | Phase Ib trials initiated |
Bonti | EB-001 | scar reduction | Phase II trials initiated |
AbbVie | JAK1-selective inhibitor | adult patients with moderate to severe atopic dermatitis | Phase II trials initiated |
IRX Therapeutics | IRX-2 | squamous cervical intraepithelial neoplasia 3 or vulvar intraepithelial neoplasia 3 | Phase II trials initiated |
Glenmark Pharmaceuticals | GBR 830 | moderate to severe atopic dermatitis | Phase IIa trials initiated enrolling 64 subjects |
Centrexion Therapeutics | CNTX-4975 | Chronic moderate to severe knee osteoarthritis | Phase III trials initiated enrolling 325 subjects |
AstraZeneca | IMFINZI® | unresectable Stage III non-small cell lung cancer following CRT | Phase III trials initiated |
Celgene | OTEZLA \(apremilast) | active Behçet’s Disease | Phase III RELIEF trials initiated |
Vertex Pharmaceuticals Incorporated | VX-659 | cystic fibrosis | Phase III trials initiated enrolling 360 patients |
Eli Lilly | Taltz (ixekizumab) | moderate to severe genital psoriasis | Phase IIIb trials initiated enrolling 149 subjects |
Evofem Biosciences | Amphora | urogenital chlamydia infection in women | Fast Track designation granted by the FDA |
Novartis | Cosentyx (secukinumab) | moderate to severe plaque psoriasis | FDA approved label update |
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