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Home » Topics » Analysis and data insight, BioWorld Asia

Analysis and data insight, BioWorld Asia
Analysis and data insight, BioWorld Asia RSS Feed RSS

Rendering of Beijing Hanmi’s 498,165-square-foot China hub

Hanmi Pharm invests ₩140B to grow China production, R&D base

Dec. 10, 2024
By Marian (YoonJee) Chu
Beijing Hanmi Pharm. Co. Ltd. broke ground on a ₩140 billion (US$98.65 million) large-scale project to build a near-500,000-square-foot China base near Beijing Capital International Airport in efforts to increase the company’s local production, R&D and office capabilities.
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Jun R. Huh at Healthcare Innovation Forum 2024

HIF 2024: Immune system could be key to neurodegenerative disease

Dec. 3, 2024
By Marian (YoonJee) Chu
Our immune cells are not just “defenders” against deadly viruses and pathogens but also a great balancer for tissue homeostasis. For neurological disorders, understanding the neuro-immune axis could be key to treating previously untreatable conditions such as autism spectrum disorder, according to Jun R. Huh, professor of immunology at Harvard Medical School.
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Celltrion building and skyline

Celltrion to expand CRDMO business, hit ₩10T sales in 2027

Dec. 3, 2024
By Marian (YoonJee) Chu
South Korean billionaire and chairman of Celltrion Group Jungjin Seo is returning Celltrion Inc. to its contract manufacturing organization (CMO) roots, as it relies on biosimilar sales to anchor the company in a fiercely competitive novel drug R&D arena.
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Global handshake silhouette

Kura, Kyowa Kirin to co-develop ziftomenib in $1.49B deal

Nov. 26, 2024
By Tamra Sami
Kura Oncology Inc. and Kyowa Kirin Co. Ltd. have joined hands in a global strategic collaboration worth $1.49 billion to develop and commercialize ziftomenib, Kura’s selective oral menin inhibitor for treating patients with acute myeloid leukemia (AML) and other hematologic malignancies.
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FDA Approved seal
Biopharma regulatory actions and approvals October 2024

Two Stelara biosimilars among 15 US FDA approvals in October

Nov. 26, 2024
By Amanda Lanier
The U.S. FDA approved 15 drugs in October, marking a decline from 24 in September and 22 in August. Despite the drop, the 2024 monthly average stands at about 19 approvals, exceeding last year’s average of 16, 2022’s 12.5, and the 17-per-month averages recorded in both 2021 and 2020.
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Gold wireframe handshake
Biopharma deals October 2024

Biopharma deal value, down for year, surges 72% in October

Nov. 19, 2024
By Amanda Lanier
Biopharma deal activity in October totaled $22.31 billion, marking a 72% jump from $13.01 billion in September. Year-to-date deal values have decreased by 2%, from $175.29 billion during the first 10 months of 2023 to $171.77 billion in the same period this year, positioning 2024 as the second-highest year on record, according to BioWorld.
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IPO, coins, upward arrow
Biopharma financings October 2024

Biopharma IPOs raise nearly $1B in October from 5 public debuts

Nov. 12, 2024
By Amanda Lanier
Biopharma financing continued to excel through the first 10 months of 2024, reaching $93.64 billion, a 53% increase from $61.04 billion during the same period in 2023.
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Liver illustration

GLP-1s push into MASH as semaglutide 2.4 mg hits endpoints

Nov. 12, 2024
By Marian (YoonJee) Chu
Positive findings from a phase III trial of semaglutide in metabolic dysfunction-associated steatohepatitis (MASH) is moving Novo Nordisk A/S to expand the glucagon-like peptide-1 (GLP-1) agonist’s indications in the U.S. and Europe, the Danish pharma said, as the MASH field sights more novel therapies.
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Clinical trial virtual display
Biopharma clinical updates September 2024

September conferences deliver wave of positive clinical updates

Oct. 29, 2024
By Amanda Lanier
In September 2024, BioWorld recorded 252 clinical trial updates, up from 92 in August, due in part to news from the European Society for Cardiology Congress, the IASCLC World Conference on Lung Cancer and the European Association for the Study of Diabetes, among others. The month included 35 successful phase III trial updates and four failures.
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Stem-cells2.png

Japan mulls ways to boost cell, gene therapy approvals

Oct. 22, 2024
By Marian (YoonJee) Chu
The Japanese government, industry and academia are deliberating health care policies and initiatives to boost Japan’s role in the future of regenerative medicine, experts at Bio Japan 2024 said, as the fruits of cell and gene therapy research come to fruition with new approvals.
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