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BioWorld - Sunday, January 18, 2026
Home » Keywords » Neurobo Pharmaceuticals Inc.

Items Tagged with 'Neurobo Pharmaceuticals Inc.'

ARTICLES

Novo Nordisk to launch Wegovy in South Korea mid-October

Oct. 7, 2024
By Marian (YoonJee) Chu
Danish pharma giant Novo Nordisk A/S is set to launch its blockbuster glucagon-like peptide-1 therapy, Wegovy (semaglutide), in South Korea’s growing obesity therapeutics market next week, a company official confirmed to BioWorld.
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Neurobo stock falls on phase I obesity data for DA-1726

Oct. 2, 2024
By Marian (YoonJee) Chu
Neurobo Pharmaceuticals Inc., of Cambridge, Mass., reported top-line phase Ia study results of its obesity drug candidate, DA-1726, Sept. 30, causing the company’s shares to lose 11.7% of their value over two days.
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Doctor pointing at liver

BIX 2024: From graveyard to breakthrough, MASH candidates on rise

July 16, 2024
By Marian (YoonJee) Chu
Nonalcoholic steatohepatitis was renamed, for the first time in 34 years, to metabolic dysfunction associated steatohepatitis (MASH), but a name change is far from being the biggest development in the field, according to experts at Bioplus Interphex (BIX) Korea 2024.
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Doctor pointing at liver

BIX 2024: From graveyard to breakthrough, MASH candidates on rise

July 11, 2024
By Marian (YoonJee) Chu
Nonalcoholic steatohepatitis was renamed, for the first time in 34 years, to metabolic dysfunction associated steatohepatitis (MASH), but a name change is far from being the biggest development in the field, according to experts at Bioplus Interphex (BIX) Korea 2024.
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Neurobo’s obesity drug nabs an FDA IND and a stock boost

Feb. 1, 2024
By Lee Landenberger
The U.S. FDA cleared an IND for Neurobo Pharmaceuticals Inc.’s weight loss drug, prompting the company to say a phase I study in obesity will begin sometime during the first half of this year. The stock catapulted upward on the news.
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Endocrine/Metabolic

Neurobo Pharmaceuticals submits IND in US for DA-1726

Dec. 29, 2023
Neurobo Pharmaceuticals Inc. has submitted an IND application to the U.S. FDA for DA-1726.
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