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BioWorld - Tuesday, May 12, 2026
Home » GLP-1

Articles Tagged with ''GLP-1''

Allurion swallowable gastric balloon

FDA approves Allurion’s gastric balloon system

Feb. 26, 2026
By Shani Alexander
No Comments
The U.S. FDA approved Allurion Technologies Inc.’s premarket application for its swallowable gastric balloon system, which features its Smart Capsule, for weight loss. The clearance is boon for the company as GLP-1 agonists gets increasingly adopted to treat obesity. The approval also brings to the market a new non-invasive option to patients looking for alternative ways to lose weight.
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GI-ORIS-pic-Vivtex-2-25.jpg

Vivtex’s oral drug delivery approach draws Novo in $2.1B deal

Feb. 25, 2026
By Jennifer Boggs
No Comments
Coming off a U.S. FDA approval of the first GLP-1 in pill format, Novo Nordisk A/S leaned further into oral drug delivery efforts, partnering with Vivtex Corp. to develop next-generation oral formulations of peptide and protein therapeutics in a potential $2.1 billion deal that marks the highest-profile news for Vivtex since the firm spun out of MIT in 2018.
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3D dollar sign

Ascletis raises $107M to advance oral GLP-1 to phase III trials

Feb. 24, 2026
By Tamra Sami
No Comments
Ascletis Pharma Inc. raised HK$843.53 million (US107.93 million) in a placement on the Hong Kong Stock Exchange to advance its lead program, ASC-30, a small-molecule glucagon-like peptide-1 (GLP-1) receptor agonist that can be dosed once monthly subcutaneously and once daily orally for treating obesity.
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Pills and bottle

Viking to push oral GLP-1/GIP drug into phase III obesity trial

Feb. 12, 2026
By Marian (YoonJee) Chu
No Comments
Viking Therapeutics Inc. said after-market hours Feb. 11 that it plans to advance its oral dual GLP-1/GIP receptor, VK-2735, into a phase III trial for obesity in the third quarter of 2026. VK-2735 is a novel dual glucagon-like peptide-1 and glucose-dependent insulinotropic polypeptide (GLP-1/GIP) receptor agonist.
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3D dollar sign

Ascletis raises $107M to advance oral GLP-1 to phase III trials

Feb. 11, 2026
By Tamra Sami
No Comments
Ascletis Pharma Inc. raised HK$843.53 million (US107.93 million) in a placement on the Hong Kong Stock Exchange to advance its lead program, ASC-30, a small-molecule glucagon-like peptide-1 (GLP-1) receptor agonist that can be dosed once monthly subcutaneously and once daily orally for treating obesity.
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US FDA finds ad introducing Wegovy pill misleading

Feb. 10, 2026
By Mari Serebrov
No Comments
Novo Nordisk A/S’ television ad introducing the tablet form of its weight-loss drug, Wegovy (semaglutide), to American consumers didn’t pass regulatory muster.
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Compounded weight-loss drugs hit on every side

Feb. 9, 2026
By Mari Serebrov
No Comments
True to its word, Novo Nordisk A/S filed a patent infringement lawsuit in U.S. district court against Hims & Hers Health Inc. over compounded versions of Novo’s semaglutide products.
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Trumprx screenshot

Hims in trouble, Novo says no-go as Trumprx.gov debuts

Feb. 6, 2026
By Mari Serebrov and Randy Osborne
No Comments
Trumprx.gov launched with much fanfare late Feb. 5, and the online tool brings promise for the “world’s lowest prices” on prescription drugs. Alongside the website hoopla came word from Hims & Hers Health of its own steep discounts on what’s to be the compounded version of a Trumprx-featured therapy: oral Wegovy (semaglutide) for obesity. Novo Nordisk A/S, Wegovy’s originator, vowed to fight.
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China NMPA approves Sciwind’s GLP-1 injection for diabetes

Feb. 3, 2026
By Marian (YoonJee) Chu
No Comments
Sciwind Biosciences Co. Ltd. said Jan. 30 it won Chinese approval for self-developed glucagon-like peptide-1 (GLP-1) receptor agonist, ecnoglutide (Xianyida), to treat adults with type 2 diabetes.
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Trumprx launch threatened by shutdown, kickback concerns

Feb. 3, 2026
By Mari Serebrov
No Comments
At a recent Cabinet meeting, U.S. Health and Human Services (HHS) Secretary Robert Kennedy reportedly said he expected Trumprx to probably go live within 10 days. That was Jan. 29, two days before HHS was once again forced to shut down many of its activities due to a congressional gridlock over a fiscal 2026 appropriations package to keep the department and several others open beyond Jan. 30.
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