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BioWorld - Friday, December 27, 2024
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BioWorld Science
June 22, 2018
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FDA grants QIDP designation to ACX-362E to treat C. difficile infection
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Metastatic breast cancer regression by immunotherapy with TILs enriched for neoantigen reactivity
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PTC Therapeutics presents updated preliminary data from FIREFISH
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Reata initiates first-in-human study with allosteric RORgammat inhibitor RTA-1701
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Preliminary data presented from first-in-human phase I trial on MTL-CEBPA
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First-in-human data presented for novel monoclonal anti-IL-6R-alpha antibody BCD-089
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HTX-011 receives breakthrough therapy designation and reaches primary endpoint in phase IIb studies
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Researchers present primary efficacy data on PRO-140 from CD02 study
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MaaT Pharma enters agreement for GvHD microbiome therapy
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New dUTPase inhibitors synthesized at CV6 Therapeutics
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Bristol-Myers Squibb describes glycogen synthase kinase 3 inhibitors
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Dual MetAP 2/DPP-IV inhibitors identified at Lilly
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Statins improve venetoclax anticancer activity in hematologic malignancies
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FDA grants regenerative medicine advanced therapy designation for VY-AADC
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Alpha Biopharma closes series A financing for phase II study of AZD-3759
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ACKR3 gene copy number variations linked to pregnancy loss
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Ironwood initiates phase III trials of IW-3718 in persistent GERD
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Attenuated vaccine candidate shows rapid probiotic-like protection from cholera in animal models
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Revance initiates phase III program with RT-002 injectable for cervical dystonia
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FDA accepts sBLA for Opdivo plus low-dose Yervoy for first-line NSCLC
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Phase II/III trial of NBTXR-3 in soft tissue sarcoma meets primary endpoint
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Synairgen reports interim data from phase II trial of SNG-001 in COPD
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Takeda acquires control of TiGenix
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REACH1 study of ruxolitinib in steroid-refractory acute GvHD meets primary endpoint
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FDA accepts IND for lanifibranor in patients with type 2 diabetes and NAFLD
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