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Pipeline
Company | Drug/Device | Medical Condition | Status |
---|---|---|---|
GlycoMimetics | Uproleselan (GMI-1271) | Relapsed/refractory acute myeloid leukemia | First patient enrolled in global Phase III trial |
Sollis Therapeutics | Clonidine micropellet | Sciatica pain | First patient enrolled in the RePRIEVE-CM trial |
Stallergenes Greer | Sublingual allergy immunotherapy tablet STAGR320 | House dust mite (HDM)-induced allergic rhinitis | Phase III trial met its primary endpoint with statistical significance in patients treated with STAGR320 compared to patients on placebo |
Rocket Pharmaceuticals | RP-L201 | Severe Leukocyte Adhesion Deficiency-I | FDA approved IND for Phase I trial |
Pliant Therapeutics | PLN-74809 | Primary sclerosing cholangitis | Granted Orphan Drug designation by FDA |
Allergan | Avycaz | Complicated urinary tract infections and complicated intra-abdominal infections | FDA accepted for review sNDA to expand label indication |
NovImmune S.A. | Gamifant® (emapalumab-lzsg) | Primary hemophagocytic lymphohistiocytosis | Granted approval by FDA |
Pfizer | Daurismo™ (glasdegib), to be used in combination with low-dose cytarabine (LDAC) | Newly diagnosed acute myeloid leukemia in adults 75 years or older | Granted approval by FDA |
AbbVie and Genentech | Venclexta® (venetoclax) | Newly diagnosed acute myeloid leukemia in adults 75 years or older who cannot tolerate intensive chemotherapy | Granted accelerated approval by FDA |
Synthetic Biologics | Synthetic Biologics | Antibiotic-mediated Clostridium difficile infection | Successfully completed End-of-Phase II meeting; Phase III go-ahead from FDA |
Bayer and Loxo Oncology | Vitrakvi (larotrectinib) | Solid tumors with NTRK gene fusion | Granted approval by FDA |
HighTide Therapeutics | HTD1801 | Nonalcoholic steatohepatitis | Fast Track designation granted by FDA |
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