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BioWorld - Tuesday, December 9, 2025
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BioWorld Science
Oct. 18, 2016
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Adjuvanted rabies vaccine from Yisheng Biopharma given U.S. orphan drug status for HCC
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Advaxis initiates phase III trial of ADXS-11-001 in high-risk locally advanced cervical cancer
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Celgene initiates first-in-human study of CC-90009 in relapsed or refractory AML
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Imago initiates phase I trial of IMG-7289 in patients with advanced myeloid malignancies
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Apitope regains global rights to ATX-MS-1467 from Merck KGaA
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Omeros reports phase II data for OMS-721, pursuing FDA breakthrough therapy designation
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Pfizer to begin shipping Inflectra next month
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89Zr-Girentuximab imaging evaluated in first-in-human renal cell carcinoma study
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Addex Therapeutics to initiate phase IIa trial of dipraglurant in focal cervical dystonia
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European Commission approves Onivyde
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Envisia Therapeutics releases interim data from ENV-515 phase II trial
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EMA gives orphan drug designation to Eiger's exendin 9-39
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FDA accepts NDA resubmission for sodium zirconium cyclosilicate
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Positive opinion handed down in E.U. for SomaKit TOC
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Responses seen with cabozantinib plus nivolumab in patients with genitourinary tumors
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Sichuan Haisco Pharmaceutical patents M3 receptor antagonists and/or beta2-adrenoceptor agonists
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Mutabilis discloses beta-lactamase inhibitors
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Takeda Pharmaceutical describes MGL inhibitors
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Jubilant Biosys develops HUNK1 inhibitors
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Toray Industries presents kappa-opioid agonists
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Regeneron and Teva update status of fasinumab programs
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MYH7 mutations may be involved in nemaline myopathies with cardiomyopathy
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PTC Therapeutics offers U.S. and E.U. regulatory update on Translarna
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RYR3 variants may cause nemaline myopathy and fiber type disproportion
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Zynerba offers updates on lead programs ZYN-001 and ZYN-002
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Brain imaging successful with [11C]CB-184 in healthy human subjects
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