2 月 26, 2024

The Chairman/CEO of HanchorBi Inc : Scott Liu is awarded as “30 Best CEOs of the Year 2024”

Our mission is to transcend immuno-oncology therapies by developing cutting-edge designer biologics with novel modalities: Dr. Scott Liu of HanchorBio Inc.


“I envision that in five years, HanchorBio to be one of the leading biotech companies in immuno-oncology in the world through the development of safe and efficacious cutting-edge designer biologics with novel modalities.” 

HanchorBio Inc. is a global biotechnology company pioneering the development of next-generation immunotherapies. Dr. Liu Scott founded the company in 2020 who currently serves as its chairman and CEO.

HanchorBio is headquartered in Taipei, Taiwan.

The Silicon Review reached out to Dr. Liu, founder, chairman, and CEO of HanchorBio Inc., and here’s what he had to say.

Interview Highlights

How would you describe your professional journey so far? Tell us about a few roadblocks and learning lessons that helped you grow through the years.

I feel that I am very blessed throughout my career. There are quite a few challenges and roadblocks during my tenure at Shanghai Henlius, however, we were always able to overcome the challenges and reach key milestones. For example, for the series B financing for Henlius, the Board of Directors suddenly decided to double the pre-money valuation from approximately $650 million to 1.3 billion, and thus made the fundraising very difficult since many investors simply did not accept such a sudden and dramatic increase. It took me more than four months of consistent efforts and door-knocking to be finally able to secure a lead investor and close the series B with a total of $190 million raised. The lesson learned here is that CEO needs to have faith in the judgement of the BoD whose collective experience and wisdom is usually much evident than that of the CEO himself. Also, any seemingly difficult tasks and obstacles can be overcome with consistent, highly focused team effort; wherever there is a will, there is a way.

Another obstacle I have repeatedly encountered over my career is delays in regulatory approval of clinical trial applications or market authorization applications. In most cases, through continuous dialogues and discussions with the regulatory agencies, we were able to resolve the issues and obtain the final regulatory approvals. The lessons learned here is that persistency and grit will eventually prevail. With solid scientific data as a foundation, one can always overcome regulatory concerns. We simply need to have faith in regulatory agencies, especially in that their decision will eventually be science-driven and data-based.

Q. Trust is one of the most important currencies of leadership that requires authenticity and consistency to maintain. What’s your take on this?

Trust is a crucial element for successful leadership. Building trust requires time, as team members need to consistently witness alignment between your words and actions. An effective leader should establish a managerial philosophy and core values alongside a mission and vision. Wholeheartedly and passionately embracing these guiding principles, both verbally and through actions, is essential for building trust. Without such dedicated and continual commitment, it becomes challenging to foster trust within the team.

Q. As the CEO of the company, what are your major roles and responsibilities?

The Chief Executive Officer holds a pivotal position in the leadership and management of a company. My primary and most significant duty to HanchorBio is to formulate the vision, mission, and core values that will serve as the guiding principles for the organization. It is important for me to consistently advocate for the mission, vision, and core values, showcasing my fervor towards them and fostering a cohesive team that trusts their leader. Every decision I make will be rooted in these Core Values, aligning with the fulfilment of the company’s mission and vision.

In addition, I shoulder the responsibility of co-establishing strategic plans with the team to execute our mission in a timely and effective manner. Fundraising, financial oversight, and the management of stakeholder relationships also fall under my purview. These responsibilities hold immense significance as maintaining a consistent and ample flow of financial support is fundamental to the success of innovative drug development.

Another significant aspect of my role involves ensuring the successful recruitment of industry veterans for executive and senior scientist positions. I also need to make sure that sound HR systems and value-driven corporate culture are established so that teams at all levels work together seamlessly and cohesively towards our goals and objectives.

Q. What can you tell us about HanchorBio? What are its focus areas?

HanchorBio is a clinical-stage global biotech, focusing on the research and development of novel biologics in Immuno-Oncology. Our mission is to transcend immuno-oncology therapies by developing cutting-edge designer biologics with novel modalities. Our core technology platform, ‘Fc-based Design of Biologics (FBDB™)’, represents a unique design of biologics targeting multiple cancers or tumors. The biologics from the platform have the capability to simultaneously activate both the innate immune system and adaptive immune system to eliminate tumor growth. Through breakthroughs in multifunctional innovative molecular configurations during the research and development process, as well as the optimization of chemistry, manufacturing, and controls (CMC) during process development, HanchorBio aims to address unmet medical needs with its innovative biologics and core technology, the FBDBs.

Currently, there are more than eight innovative projects (biologics)based on the FBDB platform in HanchorBio’s pipeline. Except for the first leading biologic in clinical trials at US and Taiwan hospitals, other first-in-class candidates are also planned to enter clinical stages soon.

Q. Can you introduce us to your FBDB platform? What are its key features?

The FBDB (Fc-Based Designer Biologics) platform, which primarily utilizes the antibody Fc region as a backbone and integrates various engineered anti-cancer molecules onto this Fc backbone. These anti-cancer molecules are developed and pioneered with the Ligand Trap technology, which involves protein engineering modifications of immune cell receptors to create engineered receptors that closely resemble their native counterparts. By fusing these engineered receptors with Fc backbone to configure a novel biologic, when administered to the patients, it can specifically target ligands in the tumor micro-environment and activate the immune systems. This enables and synergizes immune cells such as Macrophages and T cells to work together to recognize, engulf, and attack tumor cells, leading to the elimination of tumor cells.

Q. How do you see HanchorBio changing in five years, and how do you see yourself creating that change?

I envision that in five years, HanchorBio to be one of the leading biotech companies in immuno-oncology in the world through the development of safe and efficacious cutting-edge designer biologics with novel modalities. I also envision that through solid clinical trial data and FDA approval of our novel FBDB product, we will be able to bring renewed hope and optimism to millions of cancer patients worldwide. Through such an achievement, HanchorBio will hopefully become an admired company that transforms innovative drug development.

I will play a crucial role in achieving the five-year objectives; I will establish myself as a trustworthy leader who has strong leadership and an outstanding track record that attracts financial resources and top-notch talents. I will also lead the team to consistently deliver on our promises to the stakeholders and accomplish all the operational goals and key milestones in a timely fashion.

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Scott Liu, Ph.D. | Founder, Chairman, & CEO

As a life-science entrepreneur and successful biotech company-builder, Scott Liu was one of the global partners of Fosun International Limited and a co-founder, president and CEO of Shanghai Henlius Biotech Inc., a commercial-stage global biopharmaceutical company with the focus on high-quality, affordable, and innovative biologic medicines, listed on Hong Kong Stock Exchange (2696.HK) with a market value of over US$ 1.1 Billion. During his tenure with Henlius, Scott has led multiple product development initiatives (over 30 biosimilars, novel monoclonal antibodies and bispecific antibodies) and successfully launched five commercial monoclonal antibody products in China and Europe.

Scott has over 30 years of experience in managing corporate development, strategic portfolios, equity, cGMP quality operation, and CMC regulatory affairs. He has been instrumental in the development of the Technical Guidelines for the Research, Development and Evaluation of Biosimilars to promote globalization of the biopharmaceutical industry in China. Additionally, he has participated in development of multiple biological medicines, including Orencia® (for rheumatoid arthritis), Vectibix® (for colorectal cancer), Hanlikang® (rituximab biosimilar), Hanquyou®/Zercepac® (trastuzumab biosimilar), Handayuan® (adalimumab biosimilar), Hanbeitai® (bevacizumab biosimilar) and Hansizhuang® (serplulimab, novel anti-PD1).

Prior to founding HanchorBio and Henlius, Scott has previously served in several executive positions such as Vice President of Scientific Affairs at United Biomedical Inc., the Founding Director of the Biologics Quality Control Department at Bristol-Myers Squibb (Syracuse, USA), and the Director of Quality Analytical Laboratories at Amgen (Fremont, USA). Scott has authored or co-authored multiple scientific papers and has been invited as a speaker in conferences with topics ranging from Biologics Process Development, Biomanufacturing, Oncology Biologics and Immuno-Oncology.

Scott received his Ph.D. in biology at Purdue University and he completed his post-doctoral training at Stanford University.

“Our core technology platform, ‘Fc-based Design of Biologics (FBDB™)’, represents a unique design of biologics targeting multiple cancers or tumors.”

Our mission is to transcend immuno-oncology therapies by developing cutting-edge designer biologics with novel modalities.


Reference:

7 月 24, 2023
HANCHORBIO ANNOUNCES TAIWAN FDA IND APPROVAL FOR THE MULTI-REGIONAL CLINICAL TRIAL OF HCB101 TO TREAT SOLID AND HEMATOLOGICAL MALIGNANCIES 台灣食藥署批准 HCB101 治療實體瘤和血液惡性腫瘤的多地區臨床試驗
HanchorBio Inc., a global clinical-stage biotechnology company developing innovative immuno-biomedicines, announced today that the Taiwan Food and Drug Administration (TFDA) has approved its investigational new drug (IND) application to initiate a multi-regional clinical trial of its independently-developed novel drug candidate, HCB101, for the treatment of patients with advanced solid tumors or relapsed and refractory non-Hodgkin lymphoma.以開發創新免疫生物藥物的全球臨床階段生技公司-漢康生技今天宣布,台灣衛生福利部食品藥物管理署 (TFDA) 已批准其在研新藥申請 (IND),以開展獨立研發的新藥候選物 HCB101 的多區域臨床試驗,用於治療晚期實體瘤或復發難治性非霍奇金淋巴瘤患者。
6 月 28, 2024
HANCHORBIO ANNOUNCES US FDA CLEARANCE OF IND APPLICATION FOR HCB301 TRI-SPECIFIC FUSION PROTEIN TO TREAT SOLID AND HEMATOLOGICAL MALIGNANCIES
HanchorBio Inc. announced that the U.S. Food and Drug Administration (FDA) has cleared the Company’s investigational new drug (IND) application to initiate a multi-regional clinical trial of its independently developed novel drug candidate, HCB301 today.HCB301-101 is a multiregional, multicenter, open-label, dose-finding, first-in-human (FIH) study of adults with advanced solid tumors or relapsed and refractory classical Hodgkin lymphomas in the US, Australia, and Taiwan. The study evaluates the safety, tolerability, pharmacokinetics, and preliminary clinical efficacy of weekly HCB301 intravenous injections. The HCB301 IND is on track to be reviewed by the Australia Therapeutic Goods Administration (TGA) and the Taiwan FDA.漢康生技(HanchorBio Inc.)今天(2024/06/29) 宣佈自主研發的創新型候選藥物HCB301獲得美國FDA授予的新藥臨床試驗(IND)許可,即將開展多地區多中心的臨床試驗。目前於美國、澳大利亞和臺灣開展的多國多中心、非盲、劑量探索的首次人體(FIH)臨床試驗,用於治療晚期實體瘤或復發頑固型經典型霍奇金淋巴瘤的成年患者。研究目的是評估HCB301靜脈注射的安全性、耐受性、藥代動力學和初步臨床療效。HCB301的新藥臨床試驗申請(IND)目前正在接受澳大利亞藥品管理局(TGA)和臺灣TFDA的審查。