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REMEGEN

119.900

+1.9001.61%

Volume:3.76M

Turnover:446.15M

Market Cap:67.58B

PE:81.00

High:120.300

Open:118.800

Low:114.600

Close:118.000

52wk High:126.600

52wk Low:32.600

Shares:563.61M

HK Float Shares:208.58M

Volume Ratio:0.76

T/O Rate:1.80%

Dividend:- -

Dividend Rate:- -

EPS(LYR):1.480

ROE:25.37%

ROA:1.37%

PB:16.32

PE(LYR):81.00

PS:18.11

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Overview Company News Filings

RemeGen Schedules 28 April 2026 Board Meeting to Review Q1 2026 Unaudited Results

Bulletin Express

CATL Reports 48.52% Surge in Q1 Net Profit to RMB 20.74 Billion

National Data Administration Proposes Token Trading Exploration; Central Bank Adjusts Overseas Loan Ratios

Remegen Receives $650 Million Upfront Payment from AbbVie for RC148 Exclusive Licensing Agreement

Stock Track | REMEGEN Soars 5.17% Intraday on New Drug Approval and Strong Earnings Turnaround

BUZZ-RemeGen set for best day in two weeks on China nod for tumour drug application

RemeGen Drug Approved For Cancer Indication

MT Newswires Live

Stock Track | REMEGEN Soars 5.09% Intraday on New Drug Approval and Strong Revenue Growth

Hong Kong Grants First Stablecoin Issuer Licenses as Iran-US Talks Show Major Rifts

RemeGen receives NMPA approval for Disitamab Vedotin + Toripalimab in HER2-expressing urothelial carcinoma, securing fifth on-label use

Bulletin Express

RemeGen Maintains 564.48 Million Share Capital; Confirms Public Float Compliance for March 2026

Bulletin Express

RemeGen (HKG:9995) Is Posting Healthy Earnings, But It Is Not All Good News

Simply Wall St.

China International Capital Corp. Highlights Positive Trends in Domestic Innovative Drug Sector, Anticipates Key Academic Developments in 2026

China International Capital Corporation Maintains Outperform Rating on REMEGEN, Raises Target Price to HK$133.7

Lilly's Oral GLP-1 Weight Loss Drug Receives FDA Approval, Offering Daily Pill Alternative to Injections

RemeGen (SEHK:9995) Is Up 30.0% After New HER2-Low Breast Cancer Approval Has The Bull Case Changed?

Simply Wall St.

RemeGen Receives Chinese Regulatory Nod for RC288 Clinical Trial

MT Newswires Live

Stock Track | RemeGen Soars 5.07% Intraday Following NMPA Approval for Phase I/IIa Trial of Bispecific ADC RC288

RemeGen secures NMPA green light for Phase I/IIa trial of bispecific ADC RC288 targeting PSMA/B7H3

Bulletin Express

Remegen Receives Clinical Trial Approval for Bispecific ADC Drug RC288

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