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BioWorld - Tuesday, June 30, 2026
Home » Newsletters » BioWorld Asia

BioWorld Asia

June 25, 2024

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IPO puzzle pieces

China’s Ascentage drafts confidential IPO for dual listing in US

Suzhou, China-headquartered Ascentage Pharma Group Corp. Ltd. has filed plans for a confidential IPO to the U.S. SEC for a potential dual listing on both the U.S. and Hong Kong stock exchanges. News of the U.S. IPO came just a few days after Ascentage drew a $75 million equity investment from Osaka, Japan-headquartered Takeda Pharmaceutical Co. Ltd. with the issuance of about 24.3 million shares at a purchase price of HK$24.09 (US$3.08) per share. Read More

Fosun Pharma to buy out Henlius in $691.7M merger deal

Shanghai Fosun Pharmaceutical Co. Ltd announced it will buy out partner Shanghai Henlius Biotech Inc. for up to HKD$5.4 billion (US$691.7 million), according to a joint announcement on the Hong Kong Stock Exchange. Read More
fatty-liver-disease.png

Innovent’s mazdutide reduces liver fat content in obese patients

Innovent Biologics Inc.’s glucagon-like peptide-1 receptor and glucagon receptor dual agonist, mazdutide, saw 80% reduction in liver fat content in patients with more than 10% liver fat content in the phase III Glory-1 obesity trial. Read More
Deal handshake with coin, chart background

Aprilbio, Evommune strike $475M deal for autoinflammatory drug

Aprilbio Co. Ltd. saw its stock surge 30% June 20 after announcing a potential $475 million (₩655.88 billion) deal with Evommune Inc. for autoimmune disease drug candidate APB-R3. Read More
Non-Hodgkin lymphoma cells in the blood flow

China’s NMPA clears Dizal’s golidocitinib in T-cell lymphoma

China’s National Medical Products Administration (NMPA) approved Dizal Pharmaceutical Co. Ltd.’s golidocitinib for treating adults with relapsed or refractory peripheral T-cell lymphoma whose disease has progressed or was refractory to at least one prior systemic therapy. Read More

Takeda moves mezagitamab to phase III in thrombocytopenia

Takeda Pharmaceutical Co. Ltd. is progressing mezagitamab to phase III trials after the CD38 monoclonal antibody showed rapid and sustained increases in platelet counts in patients with persistent or chronic primary immune thrombocytopenia (ITP) in a phase IIb trial. Read More

Théa ends deal with Olix, returns rights of ocular drugs

France’s Théa Open Innovation, a subsidiary of Laboratoires Théa SAS, terminated its licensing agreement with South Korea’s Olix Pharmaceuticals Inc., and returned global rights of Olix’s ocular small interfering RNA (siRNA) biologic agents, OLX-301D and OLX-301A. Read More

Biotron’s BIT-225 meets endpoints in phase II HIV trial

Preliminary data show Biotron Ltd.’s lead compound BIT-225 met the primary objectives of the phase II BIT225-011 trial, a longitudinal, open-label trial designed to characterize the effect of the compound added to ongoing, suppressive antiretroviral therapy in HIV-1-infected, treatment-experienced patients who achieved only partial immune reconstitution. Read More

No sweat: FDA approves Botanix’s axillary hyperhidrosis NDA

The U.S. FDA has approved the NDA for Sofdra (sofpironium) for treating excessive underarm sweating from Botanix Pharmaceuticals Ltd. The approval was based on two pivotal phase III studies and is approved for those ages 9 and older. Read More
Businesspeople shaking hands, meeting with cityscape, charts

Deals bring $3B+ for Ascidian, Belharra, Mabcare

Following a day of deals that collectively bring a potential $3.75 billion into three biopharma companies – namely Ascidian Therapeutics Inc., Belharra Therapeutics Inc. and Mabcare Therapeutics – researchers will be busy discovering new therapies for neurological and immunological diseases, and advancing globally a candidate for solid tumors. Read More
3D illustration demonstrating antibody-drug conjugate.

Companies to Watch: Seven ADC companies under the radar

The annual Companies to Watch report, which was just released, looks closely at seven companies flying under the radar that are developing antibody-drug conjugates (ADCs) for treating cancer. Companies examined in the new report are Adcendo ApS, Araris Biotech AG, Go Therapeutics Inc., Heidelberg Pharma AG, Pheon Therapeutics Ltd., Tallac Therapeutics Inc. and Tubulis GmbH. Read More
FDA-approved-stamp4.png

Two Eylea biosimilars among 11 FDA drug approvals in May

In May, the U.S. FDA approved 11 new drugs, a significant drop from the 26 approvals in April, which was the sixth-highest monthly total since 2016. This also falls short of March’s record-setting 30 approvals, the highest number recorded by BioWorld. Read More

In the clinic for June 25, 2024

Clinical updates from Asia, including trial initiations, enrollment status and data readouts and publications: Clover, Carsgen, Daewoong, Hightide, Hutchmed, Takeda. Read More

Financings for June 25, 2024

Biopharmas in Asia-Pacific raising money in public or private financings: Ascentage, Opthea, Recce, Takeda. Read More

Other news to note for June 25, 2024

Biopharma happenings in Asia-Pacific including deals and partnerships, grants, preclinical data and other news in brief: Alivexis, Ionis, Kactus, Melodia, Otsuka, Yoltech Read More

Regulatory actions for June 25, 2024

Regulatory snapshots, including drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations in Asia-Pacific: Dizal, Innocare, Junshi, Medilink. Read More

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