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BioWorld - Friday, December 5, 2025
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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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