Hong Kong Exchanges and Clearing Limited and The Stock Exchange of Hong Kong Limited take no responsibility for the contents of this announcement, make no representation as to its accuracy or completeness and expressly disclaim any liability whatsoever for any loss howsoever arising from or in reliance upon the whole or any part of the contents of this announcement.

(Incorporated in the Cayman Islands with limited liability)

(Stock Code: 1061)

VOLUNTARY ANNOUNCEMENT

FURTHER UPDATE IN RELATION TO THE CO-DEVELOPMENT OF

THE LICENSED PRODUCT WITH HENLIUS

RELATING TO THE TREATMENT OF

EXUDATIVE (WET) AGE-RELATED MACULAR DEGENERATION

Reference is made to the announcement of Essex Bio-Technology Limited ("Company") dated 15

October 2020 ("Announcement") in relation to the Co-Development License Agreement entered into between the Licensee (both are wholly-owned subsidiaries of the Company) with Shanghai Henlius Biotech, Inc. ("Henlius") for the co-development of, and the grant to the Licensee of the exclusive rights relating to, the Licensed Product in accordance with the terms of the Co-Development License Agreement. Reference is also made to the announcement of the Company dated 29 January 2021 in relation to certain updates thereon. The Licensed Product is a pharmaceutical product that will contain at least HLX04-O-wAMD as a drug substance, which is intended for the treatment of exudative (wet) age-related macular degeneration ("wet-AMD"). Unless otherwise specified, capitalised terms used in this announcement shall have the same meanings as those defined in the Announcement.

Further update on the development relating to HLX04-O

Based on the information provided by Henlius, the application by Henlius for clinical trial for recombinant anti-vascular endothelial growth factor (anti-VEGF) humanised monoclonal antibody ophthalmic injection HLX04-O ("HLX04-O") for the treatment of wet-AMD has been recently approved by the United States Food and Drug Administration.

As informed by Henlius, the phase 3, global and multi-centre clinical study of HLX04-O is intended to commence in the near future to further evaluate the efficacy and safety of HLX04-O for the treatment of wet-AMD. According to the protocol of the clinical study, there will be 388 patients from countries/ regions including the PRC, Australia, Russian Federation, Singapore, Spain and Poland enrolling in the study.

Information about HLX04-O

Based on the information provided by Henlius, (i) HLX04-O is a new ophthalmic preparation product developed based on HLX04, a bevacizumab biosimilar independently developed by Henlius, through optimising the prescription, specifications and production processes of HLX04 according to the requirements of ophthalmic drugs, without changing the active ingredients, and is intended to be used for the treatment of wet-AMD; (ii) by means of comparability studies, it is shown that changes in production processes and prescriptions of the preparation have no adverse impact on the quality, safety and efficacy of the pharmaceutical preparation. The primary action mechanism of HLX04-O is to inhibit VEGF's binding to its receptor Flt-1 and KDR on endothelial cells to inhibit the activation of its tyrosine kinase signaling pathway, inhibit endothelial cell proliferation and reduce angiogenesis, thereby treating eye diseases associated with angiogenesis; and (iii) in January 2021, HLX04-O for the treatment of wet-

AMD has been approved to commence the phase 3 clinical trial in Australia.

Current Market Condition

As of the date of this announcement, to the knowledge of the Directors, none of the bevacizumab products marketed globally has shown wet-AMD indications.

Based on the information provided by Henlius, (i) large molecule drugs targeting wet-AMD indications that have been marketed globally include Eylea® (Aflibercept), Lucentis® (Ranibizumab) and Langmu® (Conbercept); and (ii) according to the statistics released by IQVIA MIDASTM, being the world's leading provider of professional information and strategic consulting services in the pharmaceutical and healthcare industry, the sales of relevant drugs in 2020 were as follows: US$6,071 million for Eylea®, US$3,905 million for Lucentis® and US$106 million for Langmu®.

On behalf of the Board Essex Bio-Technology Limited

Ngiam Mia Je Patrick

Chairman

Hong Kong, 19 March 2021

Executive directors of the Company as at the date of this announcement are Mr. Ngiam Mia Je Patrick, Mr. Fang Haizhou, Mr. Ngiam Hian Leng Malcolm and Ms. Yau Lai Man. Independent non-executive directors of the Company as at the date of this announcement are Mr. Fung Chi Ying, Mr. Mauffrey Benoit Jean Marie and Ms. Yeow Mee Mooi.

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Essex Bio-Technology Limited published this content on 19 March 2021 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 19 March 2021 12:12:04 UTC.