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BioWorld - Friday, December 5, 2025
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BioWorld Science
Dec. 21, 2017
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GD116 demonstrates enhanced antitumor efficacy in human breast cancer models
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U.S. Dept. of Health & Human Services describes FLT3-specific chimeric antigen receptors
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EpiVax receives grant to develop therapy for Graves disease
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Promising phase I data for CK-2127107 in healthy subjects
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Rhizen's tenalisib given orphan drug designation for peripheral T-cell lymphoma
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FDA gives Cu(II)-ATSM orphan drug status for ALS
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Eloxx Pharmaceuticals and Sevion Therapeutics complete acquisition
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JSR Corporation to acquire Crown Bioscience International
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Novel SCN2A gene mutations tied to intractable epilepsy
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First clinical results reported for CAR T cells targeting CD123
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Ticagrelor well tolerated in phase II pediatric sickle cell disease trial
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Loxo Oncology starts rolling NDA submission for larotrectinib
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TARIS and BMS agree to test combination therapy for muscle invasive bladder cancer
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Arrowhead Pharmaceuticals applies to conduct first-in-human study of ARO-AAT
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Cadent Therapeutics identifies novel potassium channel modulators
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New parkin modulators divulged by An2H Discovery
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The University of Texas discloses novel SHP-2 inhibitors
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NuCana BioMed discovers new cladribine derivatives
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FDA approves Macrilen for diagnosis of adult growth hormone deficiency
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FDA expands Opdivo indication
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FDA approves Perjeta for adjuvant treatment of HER2-positive early breast cancer
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AbbVie reports topline results from phase III study of upadacitinib
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Aivita initiates phase II autologous cancer immunotherapy study in ovarian cancer
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FDA grants QIDP designation to ceftobiprole for S. aureus bacteremia
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FDA accepts Seysara NDA for moderate to severe acne
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UCB reports phase IIb data on bimekizumab in psoriatic arthritis
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