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BioWorld - Sunday, December 21, 2025
Home » Topics » Diabetes, BioWorld

Diabetes, BioWorld
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Conference data for June 7, 2022: ADA

June 7, 2022
New and updated preclinical and clinical data presented by biopharma firms at the American Diabetes Association's 82nd Scientific Sessions, including: Lilly, Sernova, Vertex, Zealand.
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Conference data for June 6, 2022: ADA

June 6, 2022
New and updated preclinical and clinical data presented by biopharma firms at the American Diabetes Association's 82nd Scientific Sessions, including: Biomea, Eli Lilly, Gelesis, Vtv.
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Pancreas illustration
Newco news

Phaim Pharma poised to trial drug that resets immune system to treat T1D

May 24, 2022
By Richard Staines
Now is a good time to be involved with type 1 diabetes (T1D) research, according to a U.K. biotech that hopes to reduce or cut the need for insulin injections to treat the condition.
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Induced pluripotent stem cells

Evotec, Sernova team up to develop functional cure for type 1 diabetes

May 17, 2022
By Cormac Sheridan
Evotec AG and Sernova Corp. are joining forces in a bid to develop a functional cure for type 1 diabetes. The companies plan to file an IND early in 2024 for a combined cell therapy and medical device product comprising Evotec’s human beta cells, derived from the company’s induced pluripotent stem cell platform, and Sernova’s Cell Pouch delivery system, which provides transplanted cells with a vascularized, physiologically appropriate environment that enables them to secrete insulin and other hormones involved in regulating blood glucose levels.
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Kriya lands $270M series C as it hones gene therapy pipeline

May 16, 2022
By Lee Landenberger
Kriya Therapeutics Inc. has raised a $270 million series C financing to further develop its pipeline of gene therapies for treating cancer, ophthalmological problems, and rare and chronic diseases. The Redwood City, Calif.-based company has greatly expanded its employee roster, from about seven people to around 160 people, since its $80 million series A in May 2020 and scaled its learning-enabled tech and cloud computing abilities. It also further solidified its technology, manufacturing, R&D, and therapeutics units, something it plans to continue with the series C money.
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FDA Approved stamp

Lilly’s Mounjaro first to win US FDA approval for GLP-1 and GIP dual agonist

May 13, 2022
By Lee Landenberger
Six weeks ahead of its June 26 PDUFA date, the U.S. FDA has approved a priority NDA for Eli Lilly and Co.’s Mounjaro (tirzepatide), an injectable treatment for adults with type 2 diabetes (T2D). The once-weekly, first-in-class medicine activates both glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors, which leads to improved blood sugar control. The potential market is massive, as 462 million people across the planet have T2D. The numbers have been growing 1.4% annually as the population ages and grows more obese.
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Arecor eyes fast development for concentrated insulin product after phase I readout

April 28, 2022
By Richard Staines
Arecor Therapeutics plc has presented early stage clinical data from a novel concentrated insulin formulation, which it hopes will outperform marketed rivals by allowing lower volume and reduced frequency doses. Cambridge, U.K.-based Arecor presented data at the International Advanced Technologies and Treatments for Diabetes meeting from AT-278, an investigational meal-time concentrated (500 U/mL) novel formulation of insulin.
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Kallyope raises $236M for drugs targeting gut-brain axis

Feb. 15, 2022
By Michael Fitzhugh
Kallyope Inc., a company leveraging connections between the gut and brain to develop new medicines for diabetes, obesity and other diseases, has raised $236 million in series D financing to support its work. Readouts of early clinical data for its most advanced programs, phase I small molecules for metabolic disease and gut barrier conditions, will start to arrive later this year, company CEO and President Jay Galeota told BioWorld.
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Magnifying glass, FDA concept image

Lilly tagged for Trulicity social media post

Jan. 25, 2022
By Mari Serebrov
Eli Lilly and Co. has the dubious distinction of receiving the first untitled letter in 2022 from the FDA’s Office of Prescription Drug Promotion. The letter, sent Jan. 19 and posted this week, takes the Indianapolis-based company to task for an Instagram ad promoting Lilly’s diabetes drug Trulicity (dulaglutide).
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Glucose monitoring

PK? OK! Provention moving ahead with teplizumab’s phase III

Nov. 22, 2021
By Lee Landenberger
The FDA has removed an obstacle to Provention Bio Inc.’s development of teplizumab in treating type 1 diabetes.
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