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BioWorld - Wednesday, April 22, 2026
Home » Topics » Clinical

Clinical
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Test tube, dropper

China’s I-Mab progresses anti-CD47 monoclonal antibody, caps strong financial year

Dec. 14, 2020
By Elise Mak and Alfred Romann
Three months after completing what it said was the largest development and commercialization deal by a Chinese biotech, I-Mab Biopharma Co. Ltd. is moving the monoclonal antibody at the heart of the deal deeper into the clinic. At the end of November, Chinese regulators gave it a green light to move forward with an open-label, multicenter trial for lemzoparlimab, in combination with azacitidine.
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Coronavirus vaccine illustration

Codagenix starts human study of COVID-19 vaccine; further Sputnik data unveiled

Dec. 14, 2020
By Nuala Moran
LONDON – The U.K. Medicines and Healthcare products Agency (MHRA) has given approval for the first-in-human study of Codagenix Inc.’s COVI-VAC, a live, attenuated whole virus COVID-19 vaccine, which is engineered to be structurally identical to wild-type SARS-CoV-2, but is much slower to replicate.
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In the clinic for Dec. 14, 2020

Dec. 14, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Aerpio, Amarin, Arvinas, Astrazeneca, Bellus, Biontech, Biophytis, Caladrius, Cytokinetics, Curevac, Daiichi, Freeline, Innovent, Junshi, Kintor, Lilly, Mitsubishi Tanabe, Novartis, Odonate, Pfizer, Polyphor, Poxel, Puma, RDIF, Sanofi, Synlogic, TCR2.
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COVID-19 vaccine vials

Sanofi-GSK delay their COVID-19 vaccine development as Astrazeneca partners with Russia

Dec. 11, 2020
By Lee Landenberger
The Sanofi SA-Glaxosmithkline plc COVID-19 vaccine program is taking a step backward to recalibrate as weak interim phase I/II data showed an insufficient response in patients age 50 and older. The step is a large one, delaying a potential launch until mid-2021 at the earliest and the end of next year at the latest.
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As GPS navigates Regal route for Sellas, DCIS bid also making tracks

Dec. 11, 2020
By Randy Osborne
Wall Street seemed to respond with thumbs down to positive data from the phase II study called Vadis with Sellas Life Sciences Group Inc.’s nelipepimut-S (NPS, or NeuVax) in breast ductal carcinoma in situ (DCIS), but the apparent reaction likely had little to do with the trial findings.
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Clinical data volume decreases as COVID-19 focus remains

Dec. 11, 2020
By Karen Carey
For the first time since August, the volume of clinical data has dipped, with 388 items of phase I, II and III data in November, a 4% decrease compared with the prior month. Again, 17% of the entries during the month are focused on vaccines and therapeutics to fight the SARS-CoV-2 virus. The same percentage held true in October. The pandemic accounted for 16% of the clinical data in September, 15% in August and 16% in July.
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Disintegrating coronavirus

CSL, University of Queensland quit COVID-19 vaccine trials due to HIV antibody response

Dec. 11, 2020
By Tamra Sami
PERTH, Australia – The University of Queensland (UQ) and CSL Ltd. are abandoning their trials of an Australian COVID-19 vaccine after recipients generated HIV antibodies during phase I trials. The response means the antibodies produced by the vaccine can interfere with HIV diagnostic tests. However, there was no possibility the vaccine caused infection, and routine follow-up tests confirmed no HIV virus was present, the partners said.
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In the clinic for Dec. 11, 2020

Dec. 11, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Akari, Geron, Greenwich Lifesciences, Mitsubishi Tanabe, Prevail, Puma, Puretech Health, Scyneis, Sellas Life Sciences, Tychan.
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Sanofi-GSK delay their COVID-19 vaccine development as Astrazeneca partners with Russia

Dec. 11, 2020
By Lee Landenberger
SABCS 2020

In reversal of fortune, efti shows OS promise for metastatic breast cancer

Dec. 10, 2020
By Anette Breindl
Australian biopharma Immutep Ltd. saw its stock price jump 165% Dec. 10, as the company reported that adding its eftilagimod alpha (IMP-321, “efti”) to paclitaxel resulted in what the company called a “promising and improving” trend toward increased overall survival in women with metastatic hormone receptor-driven breast cancer.
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