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Pipeline
March 12, 2018
Company | Drug/Device | Medical Condition | Status |
---|---|---|---|
Seattle Genetics, Inc. | SGN-CD48A | Relapsed or refractory multiple myeloma | Phase I trial initiated enrolling 75 subjects |
Daiichi Sankyo Company, Ltd. | DS-8201 | HER2-expressing advanced colorectal cancer | Phase II trial initiated enrolling 50 subjects in North America, Europe and Japan |
GTx, Inc. | Enobosarm | Stress urinary incontinence (SUI) | Phase II trial initiated enrolling 18 female subjects |
InflaRx | IFX-1 | Moderate or severe Hidradenitis Suppertiva (HS) | Phase IIb trials initiated enrolling 175 subjects in the U.S., Germany, Greece, Denmark and the Netherlands |
Aimmune Therapeutics, Inc. | AR101 | Peanut allergy | Phase III trials initiated enrolling 850 subjects ages 4-49 |
Vanda Pharmaceuticals, Inc. | Hetlioz | Jet lag disorder | Phase III trials initiated enrolling 318 subjects |
Biohaven Pharmaceutical Holding Company Ltd. | Zydis ODT formulation of rimegepant | Migraine | Phase III trials initiated enrolling 850 subjects |
Bioverativ, Inc | BIVV009 | Cold agglutinin disease | Phase III trials initiated |
MeiraGTx | AAOO2 | Achromatopsia | PRIME designation grated by the EMA |
Tocagen Inc. | Toca 511 (vocimagene amiretrorepvec) & Toca FC (flucytosine) | Glioma | Orphan drug designated granted by the EMA |
InVivo Therapeutics Holdings Corp. | Neuro-Spinal Scaffold | Acute spinal cord injury (SCI) | FDA approval granted |
Polyganics | Liver and Pancreas Sealant Patch | Fluid leakage after hepato-pancreato-biliary (HPB) procedures | FDA breakthrough device designation granted |
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