Hansa Biopharma files draft SEC registration for potential US IPO
The company also plans a concurrent European private placement and intends to maintain its existing Nasdaq Stockholm listing while awaiting final regulatory approvals.
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Developer of immunomodulatory treatments for rare immunological diseases
hansabiopharma.comLast updated
In short: Hansa Biopharma secured a December 2026 FDA action date for imlifidase and entered a €115 million licensing agreement with SERB.
The company also plans a concurrent European private placement and intends to maintain its existing Nasdaq Stockholm listing while awaiting final regulatory approvals.
Press releases and appendices for the directed new share issue are available.
Highlights include €115m out-licensing deal and positive PAES data supporting full European approval.
The report covers January-June 2026, and management will review results and provide business and pipeline update.
Hansa Biopharma chose the opposite path and handed over development and commercialization rights for the transplant drug Idefirix in Europe and the MENA region when on May 19...
Hansa Biopharma announces that a confidential draft registration document has been submitted to the US SEC to enable a potential listing of American depositary receipts in...
The Swedish group has filed paperwork for a potential US NASDAQ IPO which could broaden access to investors as it prepares ...
Hansa Biopharma AB, "Hansa" (Nasdaq Stockholm: HNSA), today announced that the first commercial patient in Australia has received a living donor kidney transplant following treatment...
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