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BioWorld - Friday, December 5, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Jan. 30, 2018

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Patient enrollment ongoing in first-in-human trial of PF-06939926

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Sun Biopharma initiates first-line combination study of SBP-101 with gemcitabine and nab-paclitaxel

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FDA gives fast track status to Ensysce's PF-614

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Zika virus vaccine candidate from Takeda obtains FDA fast track designation

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Trial results support safety and activity of carotuximab + sorafenib in hepatocellular carcinoma

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ASPH marker possibly useful for CRC screening

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EMA committee recommends approval of Lamzede for alpha-mannosidosis

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United Neuroscience to develop vaccine to prevent chronic traumatic encephalopathy

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GSK-2256098/trametinib combination lacks activity in phase II PDAC study

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Innate Pharma and MedImmune collaborate to study IPH-5401 with durvalumab

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Chinese authorities approve clinical trials of ZKAB-001

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First patient with DLBCL enrolled in phase II study of Cellectar's CLR-131

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FDA awards RMAT designation to Abeona Therapeutics' EB-101

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Regeneron studies long-term safety and efficacy of evinacumab in patients with HoFH

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BL-8040 therapy impacts immune cell populations in pancreatic cancer patients

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FDA issues complete response letter for Linhaliq NDA

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Pfizer files for approval of lorlatinib in Japan

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Bristol-Myers Squibb presents novel ROCK inhibitors

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Leo Pharma divulges RORG ligands for psoriasis

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Almac Discovery discloses new Wee1 inhibitors

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Duke University patents APC-containing vaccines for cancer

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Ibentrus identifies new fusion proteins for cancer

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ProMetic Life Sciences finalizes design of phase III study of PBI-4050 in IPF

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FDA accepts revefenacin NDA

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Johnson & Johnson reviews pipeline progress of fourth quarter 2017

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Phase I data presented for JCAR-017 in B-NHL

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