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RemeGen’s Telitacicept Achieves Key Milestone in Sjögren’s Syndrome Treatment

Story Highlights
  • RemeGen’s Telitacicept met the primary endpoint in a Phase III trial for Sjögren’s syndrome.
  • The drug shows promise in addressing unmet needs and has fast track designation from the U.S. FDA.
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RemeGen’s Telitacicept Achieves Key Milestone in Sjögren’s Syndrome Treatment

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An update from RemeGen Co. Ltd. Class H ( (HK:9995) ) is now available.

RemeGen Co., Ltd. announced that its drug Telitacicept met the primary endpoint in a Phase III clinical trial for primary Sjögren’s syndrome in China. This marks a significant milestone as Telitacicept is the first BLyS/APRIL dual-target fusion protein drug to complete such a study in this field. The trial demonstrated the drug’s efficacy and safety, addressing a significant unmet clinical need in Sjögren’s syndrome treatment. The company plans to submit a Biologics License Application to the National Medical Products Administration of China and present the data at international conferences. Telitacicept has also been recommended by multiple guidelines in China and has received fast track designation from the U.S. FDA for its Sjögren’s syndrome indication.

The most recent analyst rating on (HK:9995) stock is a Buy with a HK$19.59 price target. To see the full list of analyst forecasts on RemeGen Co. Ltd. Class H stock, see the HK:9995 Stock Forecast page.

More about RemeGen Co. Ltd. Class H

RemeGen Co., Ltd. is a joint stock company incorporated in the People’s Republic of China, operating in the pharmaceutical industry. The company focuses on developing innovative biologic drugs, with a particular emphasis on autoimmune diseases and cancer therapies.

Average Trading Volume: 11,660,673

Technical Sentiment Signal: Buy

Current Market Cap: HK$38.89B

See more insights into 9995 stock on TipRanks’ Stock Analysis page.

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