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Ascentage Pharma’s Olverembatinib Phase III Trial Cleared by US FDA and EMA

Story Highlights
  • Ascentage Pharma’s olverembatinib receives US FDA and EMA clearance for a global Phase III study.
  • The POLARIS-1 trial could transform Ph+ ALL treatment with promising efficacy and safety results.
  • Looking for the best stocks to buy? Follow the recommendations of top-performing analysts.
Ascentage Pharma’s Olverembatinib Phase III Trial Cleared by US FDA and EMA

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An announcement from Ascentage Pharma Group International ( (HK:6855) ) is now available.

Ascentage Pharma has announced the clearance from the US FDA and EMA for a global Phase III study of olverembatinib in combination with chemotherapy for newly diagnosed Ph+ ALL patients. This study, known as POLARIS-1, aims to accelerate the drug’s registration in the US and Europe and has shown promising efficacy and safety results in early data. The study’s success could significantly impact the treatment landscape for Ph+ ALL, offering a new option for patients with limited current treatments.

The most recent analyst rating on (HK:6855) stock is a Hold with a HK$63.00 price target. To see the full list of analyst forecasts on Ascentage Pharma Group International stock, see the HK:6855 Stock Forecast page.

More about Ascentage Pharma Group International

Ascentage Pharma Group International is a pharmaceutical company focused on developing therapies for cancer, particularly targeting drug-resistant chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). The company is known for its third-generation BCR-ABL inhibitor, olverembatinib, which is approved in China and covered by the China National Reimbursement Drug List.

Average Trading Volume: 2,210,232

Technical Sentiment Signal: Buy

Current Market Cap: HK$23.31B

For an in-depth examination of 6855 stock, go to TipRanks’ Overview page.

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