09:50 uur 13-08-2018

Samsung Bioepis start fase 1 klinische test van SB26 Ulinastatin-Fc fusie-eiwit

INCHEON — (BUSINESS WIRE) —

  • SB26, ook bekend als TAK-671, is bedoeld voor de behandeling van ernstige acute pancreatitis.
  • SB26 is de eerste therapeutische kandidaat in de strategische samenwerkingsovereenkomst met risicodeling tussen Samsung Bioepis en Takeda om meerdere nieuwe biologische therapieën te ontwikkelen.

Samsung Bioepis Co., Ltd. kondigde vandaag aan dat het binnenkort een Fase 1 studie zal beginnen om SB26 op gezonde vrijwilligers te evalueren. SB26, ook bekend als TAK-671, is een ulinastatin-Fc (UTI-Fc)-fusie-eiwit voor de behandeling van ernstige acute pancreatitis. Niet-klinische GLP-veiligheidsstudies bij apen en ratten ondersteunden vroege studies bij de mens met SB26.

De gerandomiseerde, dubbelblinde, placebo-gecontroleerde, enkelvoudige en meervoudige dosis escalatie Fase 1 studie is ontworpen om de veiligheid, verdraagbaarheid en farmacokinetiek van intraveneuze SB26 op gezonde vrijwilligers te beoordelen. De resultaten van de Fase 1-studie worden in het derde kwartaal van 2020 verwacht.

Samsung Bioepis to Initiate Phase 1 Clinical Trial of SB26 Ulinastatin-Fc Fusion Protein

INCHEON, Korea–(BUSINESS WIRE)–

  • SB26, also known as TAK-671, is intended to treat severe acute pancreatitis
  • SB26 is the first therapeutic candidate in the risk-sharing strategic collaboration agreement between Samsung Bioepis and Takeda to co-develop multiple novel biologic therapies.

Samsung Bioepis Co., Ltd. today announced it will soon begin a Phase 1 study to evaluate SB26 in healthy volunteers. SB26, also known as TAK-671, is a ulinastatin-Fc (UTI-Fc) fusion protein intended to treat severe acute pancreatitis. Non-clinical GLP safety studies performed in monkeys and rats supported early human studies with SB26.

The randomized, double-blind, placebo-controlled, single and multiple dose escalation Phase 1 study is designed to assess the safety, tolerability and pharmacokinetics of intravenous SB26 in healthy volunteers. Results of the Phase 1 study are expected in the third quarter of 2020.

“The upcoming clinical trial marks a major milestone for those of us at Samsung Bioepis, as SB26 is set to become the first novel biologic candidate from our company to enter clinical trials,” said Chul Kim, Senior Vice President and Head of Clinical Sciences Division, Samsung Bioepis. “Acute pancreatitis remains one of the most common gastrointestinal conditions, affecting more patients every year. While mild acute pancreatitis is more easily treatable, severe acute pancreatitis, which affects approximately 20% of patients suffering from acute pancreatitis, can often be fatal. Unfortunately, treatment options remain extremely limited. By leveraging the unique strengths of our partnership with Takeda, we hope to rapidly advance SB26 through clinical trials.”

SB26 is the first therapeutic candidate in the risk-sharing strategic collaboration agreement between Samsung Bioepis and Takeda Pharmaceutical Company Limited (TSE: 4502), which brings together Samsung Bioepis’ agile biologics development platform with Takeda’s best-in-class experts in drug development to co-fund and collaboratively develop innovative therapies representing meaningful value to patients who need them.

About Samsung Bioepis Co., Ltd.

Established in 2012, Samsung Bioepis is a biopharmaceutical company committed to realizing healthcare that is accessible to everyone. Through innovations in product development and a firm commitment to quality, Samsung Bioepis aims to become the world’s leading biopharmaceutical company. Samsung Bioepis continues to advance a broad pipeline of biosimilar candidates that includes six late-stage candidates that cover the therapeutic areas of immunology, oncology and diabetes. Samsung Bioepis is a joint venture between Samsung BioLogics and Biogen. For more information, please visit: www.samsungbioepis.com.

Contacts

Samsung Bioepis Co., Ltd.
MEDIA
Mingi Hyun
+82-31-8061-1594
mingi.hyun@samsung.com

 

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