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BioWorld - Wednesday, January 21, 2026
Home » Hanmi Pharmaceutical Co. Ltd.

Articles Tagged with ''Hanmi Pharmaceutical Co. Ltd.''

Endocrine/metabolic

HM-17321, a CRFR2-selective UCN2 analogue with efficacy in models of obesity

Nov. 22, 2024
Urocortin-2 (UCN2) is a selective corticotropin-releasing factor CRF2 receptor (CRFR2) agonist, which has been previously shown to reduce fat mass while promoting muscle hypertrophy. Hanmi Pharmaceutical Co. Ltd. presented the discovery and preclinical characterization of a novel CRFR2-selective UCN2 analogue, HM-17321, being developed for the treatment of obesity.
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Cancer

SOS1 inhibitor HM-99462 demonstrates synergy with RTK-KRAS-MAPK signaling inhibitors

Nov. 8, 2024
SOS1 is a guanine nucleotide exchange factor (GEF) that activates KRAS, and recent preclinical studies have demonstrated that combining KRAS and EGFR inhibitors with SOS1 inhibitors can overcome resistance and achieve durable responses.
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Lab glassware and scientist
Cancer

HM-100760 targets MTAP-deleted cancers via synthetic lethality

Oct. 31, 2024
Methionine adenosyltransferase 2A (MAT2A), the rate-limiting enzyme in the methionine cycle, catalyzes the formation of S-adenosylmethionine (SAM) from methionine and adenosine triphosphate (ATP).
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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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Alpha-galactosidase enzyme
Endocrine/metabolic

GC Biopharma and Hanmi’s once-monthly subcutaneous treatment for Fabry disease gains US IND clearance

Sep. 3, 2024
The FDA has cleared an IND for a phase I/II trial of LA-GLA (GC-1134A, HM-15421), an innovative enzyme replacement therapy for Fabry disease being co-developed by GC Biopharma Corp. and Hanmi Pharmaceutical Co. Ltd.
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Test tube, dropper, DNA illustration
Endocrine/metabolic

US orphan drug status granted to Hanmi and GC Biopharma candidate for Fabry disease

May 28, 2024
The U.S. FDA has granted orphan drug status to HM-15421 (GC-1134A, LA-GLA) for the treatment of Fabry disease.
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Headquarter building for Hanmi

Lim brothers regain control of Hanmi, derailing Hanmi-OCI merger

April 2, 2024
By Marian (YoonJee) Chu
In a potential watershed moment for South Korea’s Hanmi Group, a hair-splitting vote at the 51st shareholder meeting favored the two sons of the late founder and Chairman Lim Sung-ki, effectively halting a merger between Hanmi and OCI Holdings Co. Ltd.
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Headquarter building for Hanmi

Lim brothers regain control of Hanmi, derailing Hanmi-OCI merger

March 28, 2024
By Marian (YoonJee) Chu
In a potential watershed moment for South Korea’s Hanmi Group, a hair-splitting vote at the 51st shareholder meeting favored the two sons of the late founder and Chairman Lim Sung-ki, effectively halting a merger between Hanmi and OCI Holdings Co. Ltd.
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Hanmi Pharmaceutical researchers

Hanmi unveils new obesity pipeline under new strategy leadership

Sep. 15, 2023
By Marian (YoonJee) Chu
Hanmi Science Co. Ltd. is rolling out a new obesity pipeline with five candidates under its relatively new leadership with Lim Ju-hyun, the eldest daughter of Hanmi Pharmaceutical Co. Ltd. founder Lim Sung-ki, who serves as president of Hanmi’s global strategy division. Songpa-gu, Seoul-based Hanmi Science is the holding group of its main drug development and production arm, Hanmi Pharmaceutical, and its wholesaler arm, Online Pharm.
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Hanmi repositions once-returned GLP-1 drug to obesity

Aug. 1, 2023
By Marian (YoonJee) Chu
South Korean pharmaceutical company Hanmi Pharmaceutical Co. Ltd. may have found its footing after its misstep with Sanofi SA in 2020 for efpeglenatide, its glucagon-like peptide-1 (GLP-1) receptor agonist. On July 31, Hanmi announced that the once-dropped drug would be developed to treat obesity in the Korean population, submitting an IND application to the MFDS on July 28 to examine the once-a-week injection efpeglenatide in a phase III trial.
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