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Pipeline
Company | Drug/Device | Medical Condition | Status |
---|---|---|---|
Inhibrx Inc. | INBRX-101 | alpha-1 antitrypsin deficiency (AATD) | Phase 1 trial initiated |
Ribon Therapeutics | RBN-2397 | cancer | Phase 1 trial initiated enrolling 2,397 subjects with various tumor types, including squamous cell carcinoma of the lung |
IPI-549 in combination with Arcus’ AB298 and Doxil | advanced triple negative breast cancer (TNBC) | Phase 1/1b trial initiated | |
Hutchison China MediTech Limited | HMPL-689 | relapsed or refractory lymphoma | Phase 1/1b trial initiated |
Rocket Pharmaceuticals, Inc. | RP-L201 | severe Leukocyte Adhesion Deficiency-I (LAD-I) | Phase 1/2 trial initiated enrolling nine pediatric subjects globally |
IPI-549 in combination with Tecentriq and Abraxane (nab-paclitaxel) | front-line triple negative breast cancer (TNBC) | Phase 2 trial initiated | |
OBI Pharma | OBI-999 | Globo H | IND approval granted by the FDA |
Magenta Therapeutics | MGTA-456 | metabolic disorders | RMAT designation granted by the FDA |
Prescient Metabiomics | LifeKit Prevent Colorectal Neoplasia Test | colorectal cancer (CRC) | Breakthrough Device designation granted by the FDA |
Ra Pharmaceuticals, Inc. | zilucoplan | myasthenia gravis | Orphan Drug designation granted by the FDA |
ApiFix Ltd. | Minimally Invasive Deformity Correction (MID-C) system | progressive adolescent idiopathic scoliosis (AIS) | HDE approval granted by the FDA |
US WorldMeds, LLC | MYOBLOC (rimabotulinumtoxinB) injection | chronic sialorrhea | sBLA approval granted by the FDA |
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