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Shanghai Henlius Biotech’s HLX17 Receives FDA Approval for Clinical Trials

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Shanghai Henlius Biotech’s HLX17 Receives FDA Approval for Clinical Trials

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Shanghai Henlius Biotech, Inc. Class H ( (HK:2696) ) has provided an update.

Shanghai Henlius Biotech, Inc. announced that the U.S. FDA has approved the investigational new drug application for HLX17, a biosimilar of pembrolizumab, for phase 1 clinical trials. This approval marks a significant step for the company as it aims to conduct international multi-center trials, potentially enhancing its position in the oncology market, where pembrolizumab sales reached approximately USD 32.056 billion in 2024.

The most recent analyst rating on (HK:2696) stock is a Buy with a HK$97.75 price target. To see the full list of analyst forecasts on Shanghai Henlius Biotech, Inc. Class H stock, see the HK:2696 Stock Forecast page.

More about Shanghai Henlius Biotech, Inc. Class H

Shanghai Henlius Biotech, Inc. operates in the biotechnology industry, focusing on the development of biosimilar drugs. The company specializes in creating recombinant humanized monoclonal antibodies for various cancer treatments, targeting a global market with significant demand for innovative oncology solutions.

Average Trading Volume: 1,403,180

Technical Sentiment Signal: Buy

Current Market Cap: HK$44.49B

See more insights into 2696 stock on TipRanks’ Stock Analysis page.

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