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BioWorld - Wednesday, January 21, 2026
Home » Topics » Immune, BioWorld Asia

Immune, BioWorld Asia
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Apimeds prices $11.5M IPO for bee venom-based therapy

Oct. 1, 2024
By Marian (YoonJee) Chu
Apimeds Pharmaceuticals US Inc., a subsidiary of Seoul, South Korea-based Inscobee Inc., is “counting down” to an official IPO on the New York Stock Exchange with its S-1 filing showing a targeted offering of $11.5 million.
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Epimab licenses BCMA bispecific to startup Vignette in $635M deal

Sep. 10, 2024
By Jennifer Boggs
In a deal that brings $60 million in cash and equity up front, plus up to $575 million in milestone payments, Shanghai-based Epimab Biotherapeutics Inc. and San Diego-based Vignette Bio Inc. entered a licensing agreement for Epimab’s BCMA-targeting T-cell engager, EMB-06, for autoimmune disease.
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Navigator raises $100M in series A for autoimmune drug

Sep. 3, 2024
By Marian (YoonJee) Chu
Navigator Medicines Inc. is charting a course through the autoimmune disease drug landscape, having raised $100 million in a series A funding round to advance an OX40 ligand (OX40L)-targeted portfolio licensed from South Korea’s Imbiologics Corp.
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Global handshake silhouette

Huadong gets China rights to Imbiologics’ Oxtima program for ₩430B

Aug. 27, 2024
By Marian (YoonJee) Chu
Imbiologics Inc. scored a potential ₩430 billion (US$315.5 million) deal with China’s Hangzhou Zhongmei Huadong Pharmaceutical Co. Ltd. for Oxtima, an autoimmune disease program with two assets co-developed by Seoul, South Korea-based HK Inno.N Corp.
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Global handshake silhouette

Huadong gets China rights to Imbiologics’ Oxtima program for ₩430B

Aug. 20, 2024
By Marian (YoonJee) Chu
Imbiologics Inc. scored a potential ₩430 billion (US$315.5 million) deal with China’s Hangzhou Zhongmei Huadong Pharmaceutical Co. Ltd. for Oxtima, an autoimmune disease program with two assets co-developed by Seoul, South Korea-based HK Inno.N Corp.
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Coronavirus, lungs, hand holding stethoscope
Respiratory

Scientists discover gene associated with recovery responses in severe respiratory viral infections

Aug. 20, 2024
By Tamra Sami
Researchers have identified a gene associated with whether patients hospitalized with respiratory viral infections recover rapidly or face life-threatening complications. The gene has the potential to be used as a diagnostic tool or biomarker, which could help triage patients suffering from severe respiratory infections. Having such a biomarker would help clinicians in their early risk assessments to manage their intervention strategies.
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Cullinan ends $625M deal, returns Harbour’s cancer drug

Aug. 13, 2024
By Marian (YoonJee) Chu
Cullinan Therapeutics Inc. terminated development of Harbour Biomed Holdings Ltd.’s bispecific B7H4 x 4-1BB immune activator, CLN-418 (HBM-7008), after reviewing phase I data.
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Concept of business partnership

Genor wins $440M+ cancer drug deal with Third Rock/Two River firm

Aug. 13, 2024
By Marian (YoonJee) Chu
China’s Genor Biopharma Co. Ltd. agreed to out-license GB-261, its bispecific antibody candidate primarily targeting B-cell lymphomas, to TRC 2004 Inc., a U.S.-based newco co-founded by Third Rock Ventures LLC and Two River Group Holdings LLC.
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Handshake with DNA, molecules

Otsuka to buy Boston chemoproteomics biotech for up to $1.1B

Aug. 6, 2024
By Marian (YoonJee) Chu
Tokyo-headquartered Otsuka Pharmaceutical Co. Ltd. said Aug. 1 that it will acquire Boston-based Jnana Therapeutics Inc. through a potential $1.125 billion M&A deal. Under the terms, Otsuka will work to close the transaction by the third quarter of 2024, with $800 million paid out to Jnana shareholders, along with up to $325 million in additional development and regulatory milestones payments.
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FDA Approved stamp with pills

Sun Pharma’s JAK inhibitor for severe alopecia gets US FDA nod

July 30, 2024
By Lee Landenberger
The U.S. FDA has approved Sun Pharmaceutical Industries Ltd.’s Leqselvi (deuruxolitinib), a JAK1 and JAK2 inhibitor for adults with severe alopecia areata, a chronic autoimmune disease. The twice-daily, oral treatment will be targeting a company-estimated market of about 300,000 people in the U.S. This is the third FDA-approved treatment for severe alopecia areata in the past three years.
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