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ASCLETIS-B

10.020

-0.230-2.24%

Volume:1.78M

Turnover:18.09M

Market Cap:10.54B

PE:-27.07

High:10.320

Open:10.150

Low:9.945

Close:10.250

52wk High:19.860

52wk Low:7.950

Shares:1.05B

HK Float Shares:1.05B

Volume Ratio:1.18

T/O Rate:0.17%

Dividend:- -

Dividend Rate:- -

EPS(LYR):-0.370

ROE:-18.45%

ROA:-14.45%

PB:4.67

PE(LYR):-27.07

PS:4454.37

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Overview Company News Filings

Ascletis Says FDA Clears Phase III Trials for Oral GLP-1 Obesity Drug ASC30

Ascletis Pharma Schedules Board Meeting to Review Interim Results, Consider Dividend

Ascletis Pharma Files HKEX Next-day Disclosure Return on Share Repurchase for Cancellation

ASCLETIS-B (01672) Spends HK$1.76 Million to Buy Back 200,000 Shares on July 29

Ascletis Pharma - Ind Applications for Asc37 Sq and Oral Formulations to be Submitted in Q3 2026

THOMSON REUTERS

Ascletis Announces Once-Monthly Subcutaneously Administered Glp-1R/Gipr/Gcgr Triple Peptide Agonist, Asc37, Demonstrated Superior Weight Loss in a Diet-Induced Obese Mouse Model

THOMSON REUTERS

Ascletis Pharma - Announces Asc37 Demonstrates Superior Weight Loss in Obese Mouse Model

THOMSON REUTERS

Ascletis’ ASC37 Triple Agonist Delivers 88% Greater Weight Loss Than Tirzepatide; Monthly Injection and Oral BLA Filings Planned for 2026

Bulletin Express

Ascletis Says ASC37 Triple Agonist Posts 88% Greater Weight Loss than Tirzepatide in Obese Mice

Ascletis Pharma Files HKEX Next-day Return Disclosing Share Repurchase for Cancellation

Ascletis Files HKEX Next-day Disclosure Return Reporting Share Repurchase for Cancellation

Ascletis Announces Oral Discussion of Asc36_35 Fdc Preclinical Data Demonstrating Superior Weight Loss to Eloralintide/tirzepatide Combination at the 62nd European Association for the Study of Diabetes (easd) Annual Meeting

THOMSON REUTERS

Ascletis Pharma Files HKEX Next-day Disclosure Return Reporting Share Repurchase for Cancellation

ASCLETIS Executes Share Buyback, Spending HK$2.58 Million on July 17

Ascletis Pharma Files HKEX Next-day Return Disclosing Share Repurchase for Cancellation

Ascletis Advances First-in-Class Oral GLP-1R/GIPR Combo; IND Filing Planned for Q4 2026

Bulletin Express

Ascletis Selects Oral Glp-1/gip Fixed-dose Combo Asc30_48 for Clinical Development in Obesity

Ascletis Pharma - Ind Submission to FDA for Asc30_48 Fdc Oral Tablets Expected in Q4 2026

THOMSON REUTERS

Ascletis Pharma - Asc30_48 Fdc Shows 52% Greater Body Weight Reduction vs Asc30 Monotherapy in Nhp Study

THOMSON REUTERS

ASCLETIS-B Chooses Fixed-Dose Combination of Pioneering Oral Small Molecule GIPR Agonist ASC48 and Oral GLP-1R Agonist ASC30 for Clinical Development

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