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BioWorld - Sunday, May 3, 2026
Home » Authors » Jennifer Boggs

Jennifer Boggs

Articles

ARTICLES

Premature posting of remdesivir data raises doubts for use in COVID-19

April 23, 2020
By Jennifer Boggs
Shares of Gilead Sciences Inc. were dented April 23 after reports surfaced that its antiviral drug, remdesivir, failed to improve the condition of patients with COVID-19.
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China remdesivir studies halted due to lack of new COVID-19 patients

April 21, 2020
By Jennifer Boggs
Two phase III studies in China testing Gilead Sciences Inc.’s antiviral drug, remdesivir, in patients with COVID-19 infection have been halted after Chinese authorities reported a lack of eligible patients. Other studies, including trials sponsored by the Foster City, Calif.-based company, remain ongoing.
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China remdesivir studies halted due to lack of new COVID-19 patients

April 15, 2020
By Jennifer Boggs
Two phase III studies in China testing Gilead Sciences Inc.’s antiviral drug, remdesivir, in patients with COVID-19 infection have been halted after Chinese authorities reported a lack of eligible patients. Other studies, including trials sponsored by the Foster City, Calif.-based company, remain ongoing.
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Ipsen falls on FDA hold for bone disorder drug palovarotene

Dec. 6, 2019
By Jennifer Boggs
News of a partial FDA clinical hold for pediatric patients after safety reports from an ongoing trial testing palovarotene in fibrodysplasia ossificans progressiva (FOP) identified cases of early growth plate closure sent shares of Ipsen SA (Paris:IPN) falling 13.6% Friday.
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Acceleron's Celgene-partnered luspatercept wins FDA nod in beta-thalassemia

Nov. 10, 2019
By Jennifer Boggs
Nearly a month ahead of the PDUFA date, red blood cell maturation drug luspatercept cleared the FDA for treating anemia in adults with beta-thalassemia who require regular red blood cell (RBC) transfusions. Branded Reblozyl, the drug, developed in a collaboration between Celgene Corp. and Acceleron Pharma Inc., is expected to be available in one week following approval.
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Ardelyx nabs FDA approval for Ibsrela in IBS-C

Sep. 13, 2019
By Jennifer Boggs
It's been a busy September for Ardelyx Inc. so far. Less than two weeks after the Fremont, Calif-based company reported promising pivotal data for tenapanor in chronic kidney disease patients with hyperphosphatemia, the sodium hydrogen exchanger 2 (NHE3) inhibitor won FDA approval for use in irritable bowel syndrome with constipation (IBS-C).
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AI microchip illustration

Transforming R&D and health care with artificial intelligence

Aug. 22, 2019
By Jennifer Boggs
The convergence of artificial intelligence (AI) and the health care sector was inevitable. The advent of machine-learning and deep-learning technologies capable of analyzing and synthesizing massive amounts of data with algorithms designed to mimic human-level decision-making seems a natural fit for an industry in dire need of greater efficiency.
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Transforming R&D and health care with artificial intelligence

Aug. 22, 2019
By Jennifer Boggs
The convergence of artificial intelligence (AI) and the health care sector was inevitable. The advent of machine-learning and deep-learning technologies capable of analyzing and synthesizing massive amounts of data with algorithms designed to mimic human-level decision-making seems a natural fit for an industry in dire need of greater efficiency.
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As investors favor oncology and rare disease, work in prevalent chronic disease takes backseat

June 7, 2019
By Jennifer Boggs
PHILADELPHIA – Compared to oncology, chronic diseases such as cardiovascular disease, diabetes and dementia represent much more substantial costs to the overall U.S. health care system, yet investment and R&D innovation in those areas has been on a steady decline over the past decade or so, according to research compiled by the Biotechnology Innovation Organization (BIO).
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Mixed reaction to glioma trial continuation sends Tocagen falling; data expected year-end

May 23, 2019
By Jennifer Boggs
Tocagen Inc.'s disclosure that the independent data monitoring board for its ongoing phase III trial in recurrent high-grade glioma (HGG) recommended the study continue without modification following a planned interim analysis drew mixed reactions from analysts and sent shares of the San Diego-based company (NASDAQ:TOCA) falling 38% Wednesday.
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View All Articles by Jennifer Boggs

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