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Pipeline
Company | Drug/Device | Medical Condition | Status |
---|---|---|---|
Nektar Therapeutics | NKTR-358 | systemic lupus erythematosus (SLE) | Phase Ib trial initiated evaluating 50 subjects |
Bonti, Inc. | EB-001T | elective abdominoplasty surgery | Phase II trial initiated |
Amneal | IPX203 | advanced Parkinson’s disease | Phase III trial initiated to enroll 500 subjects |
Prisyna, the oral care division of Synedgen | Moisyn product line | xerostomia | 510(k) clearance granted by the FDA |
C4 Imaging LLC | HDR MRI Marker | use prior to high dose rate (HDR) brachytherapy to accurately locate the position of the applicators that guide the placement of radioactive sources for the treatment of multiple cancers | 510(k) clearance granted by the FDA |
Palladio Biosciences. Inc. | lixivaptan capsules | autosomal dominant polycystic kidney disease (ADPKD) | IND clearance granted by the FDA |
Portola Pharmaceuticals | Andexxa | antidote for blood thinners rivaroxaban and apixaban | Approval granted by the FDA |
Janssen Pharmaceutical Companies of Johnson & Johnson | DARZALEX (daratumumab) in combination with VELCADE (bortezomib), a proteasome inhibitor (PI); melphalan, an alkylating agent; and prednisone - VMP | newly-diagnosed multiple myeloma who are ineligible for autologous stem cell transplant (ASCT) | Approval granted by the FDA |
PaxVax, Inc. | Chikungunya vaccine | prevention of the chikungunya virus | Fast Track Designation granted by the FDA |
Debiopharm International SA | Debio 1347 (FGFR 1-3 Inhibitor) | unresectable or metastatic tumors with a specific FGFR gene alteration | Fast Track Designation granted by the FDA |
Genentech | Tecentriq triple combination with Avastain (bevacizumab), paclitaxel and carboplatin (chemotherapy) | first-line treatement of patients with metastatic non-squamous non-small cell lung cancer (NSCLC) | Priority Review granted by the FDA |
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