Full Press Release Details
Adagene Announces Updates to its Board of Directors
SAN DIEGO and SUZHOU, China, April 28,
2023 - Adagene Inc. ("Adagene") (Nasdaq: ADAG), a platform-driven, clinical-stage biotechnology company transforming
the discovery and development of novel antibody-based therapies today announced updates to its board of directors (the "Board"),
including the following:
"We are excited to welcome Drs. Turner
and Du and Ms. Wang to our Board, as we work to advance our differentiated clinical products rapidly to reach critical value inflection
points, harvest value from our preclinical assets, and fully leverage our platform technologies to drive future growth," said Peter
Luo, Ph.D., Co-Founder, Chief Executive Officer and Chairman of the Board of Adagene.
"I am also appreciative of Lefei Sun's many contributions during his past four years of service and the contributions of Yuwen
Liu in the past year. I look forward to working with the new directors who bring a breadth of industry experience and new insights to
Adagene Inc. (Nasdaq: ADAG) is a platform-driven,
clinical-stage biotechnology company committed to transforming the discovery and development of novel antibody-based cancer immunotherapies.
Adagene combines computational biology and artificial intelligence to design novel antibodies that address unmet patient needs.
Powered by its proprietary Dynamic Precision Library (DPL) platform, composed of NEObody , SAFEbody , and POWERbody technologies,
Adagene's highly differentiated pipeline features novel immunotherapy programs. Adagene has forged strategic collaborations with
reputable global partners that leverage its technology in multiple approaches at the vanguard of science.
For more information, please visit: https://investor.adagene.com.
a registered trademark in the United States, China, Australia, Japan, Singapore,
and the European Union.
Safe Harbor Statement
press release contains forward-looking statements, including statements regarding the potential implications of clinical data for patients,
and Adagene's advancement of, and anticipated clinical activities, clinical development, regulatory milestones, and commercialization
of its product candidates. Actual results may differ materially from those indicated in the forward-looking statements as a result of
various important factors, including but not limited to Adagene's ability to demonstrate the safety and efficacy of its drug candidates;
the clinical results for its drug candidates, which may not support further development or regulatory approval; the content and timing
of decisions made by the relevant regulatory authorities regarding regulatory approval of Adagene's drug candidates; Adagene's
ability to achieve commercial success for its drug candidates, if approved; Adagene's ability to obtain and maintain protection
of intellectual property for its technology and drugs; Adagene's reliance on third parties to conduct drug development, manufacturing
and other services; Adagene's limited operating history and Adagene's ability to obtain additional funding for operations
and to complete the development and commercialization of its drug candidates; Adagene's ability to enter into additional collaboration
agreements beyond its existing strategic partnerships or collaborations, and the impact of the COVID-19 pandemic on Adagene's clinical
development, commercial and other operations, as well as those risks more fully discussed in the "Risk Factors" section in
Adagene's filings with the U.S. Securities and Exchange Commission.
All forward-looking statements are based on information currently available to Adagene,
and Adagene undertakes no obligation to publicly update or revise
any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required by law.
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