2013 International Conference on Phase 1 and Early Phase Clinical Trials

The International Conference on Phase 1 and Early Phase Clinical Trials and the pre-conference Open day of HKU Phase 1 Clinical Trials Centre were successfully held during April 25 - 26, 2013. We are honored to have 21 renowned international speakers and session chairs sharing their expertise and experience in phase 1 and early phase clinical trials with about 300 delegates from 10 countries and places in Asia-Pacific and Europe.

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  • Conference
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Phase 1 and early phase clinical trials are obviously blooming in the Asia-Pacific region. In the first session, speakers gave an overview on the latest international trends of new drug development and early clinical trials from the perspectives of international and local companies, including strategies in identifying promising new drug candidates, early clinical trials design and development, application of genomic sciences in research on personalized medicines, and the prospects of integrating the strengths of mainland China and Hong Kong in new drug research. In the second and third sessions, experts in phase 1 and early phase clinical trial operations and management openly shared their knowledge in the current clinical trial environments in Asia-Pacific and their practical experiences in operating phase 1 clinical trial centres in the region. Through the experts' sharing, it is clear that the Asia-Pacific region is ready, and will play a more important role in early development of new drugs on a global basis.

Selected presentation slides and photo snapshots are available for review below.

Once again, thanks for the support by the speakers, session chairs, and all the participants in the event.

Time
Topic Speaker
0900 – 0915
Opening Remarks Professor Karen Lam,
Chairman, Clinical Trials Centre, The University of Hong Kong
Dr. Che-Chung Luk,
Cluster Chief Executive, Hong Kong West Cluster, Hospital Authority
Session 1: International Trends and Strategies of Phase 1 and Early Phase Clinical Development
Chair: Professor Bernard Cheung, Medical Director, Phase 1 Clinical Trials Centre, The University of Hong Kong
Professor Ching-Wan Lam, Director of Drug Metabolism and Pharmacokinetics, Phase 1 Clinical Trials Centre, The University of Hong Kong
Dr. Qinyong Dai, Medical Director, Roche Hong Kong Limited
0915 – 0945
Global Strategies of Early Clinical Development Dr. Axel Riedel,
Head of Regional Clinical Operations, Asia & MENA, Boehringer Ingelheim
0945 – 1015
Novartis Portfolio: Building Future Through an Unprecedented Pipeline Dr. Jonathan Sun,
Associate Medical Director APSA, Novartis Oncology
1045 – 1115
Pharmaceutical Development in Hong Kong: Prospects and Challenges Dr. Benjamin Li,
Chief Executive Officer, Lee's Pharmaceutical
1115 – 1145
Rapid Drug Development from First-in-Human to Proof-of-Concept – New Strategies Dr. John Lambert,
Chief Medical Officer, PAREXEL Early Phase
Session 2: Regulatory and Ethical Perspectives in Phase 1 and Early Phase Clinical Trials
Chair: Professor Ian Wong, Head, Department of Pharmacology and Pharmacy, The University of Hong Kong
Professor Geng-Chang Yeh, Vice Superintendent / Director, Joint Clinical Research Center, Taipei Medical University Hospital
1315 – 1345
Risk-Benefit and Ethical Issues in Phase 1 and Non-Patient Volunteer Research Dr. Danny Soon,
Managing Director and Principal Investigator,
Lilly NUS Center for Clinical Pharmacology
1345 – 1415
New Drug Development and the Regulatory Environment in Korea Professor Young-Suk Park,
Director, Clinical Trial Center,
Research Institute for Future Medicine, Samsung Medical Center
1415 – 1445
Challenges of Early Phase Clinical Trials and Regulatory Issues in Japan Professor Yasuhisa Fujii,
CCRC Operation Head, Chiba University Hospital Clinical Research Center
Session 3: Operations and Quality Assurance for Phase 1 Clinical Trials Centres
Chair: Mr. Anthony Nguyen, Co-Director, Business & Project Acceleration Team, Regional Clinical Trial Center, Dong-A University Hospital
Dr. Creany Wong, Business Development & Project Coordination Manager, Clinical Trials Centre, The University of Hong Kong
1515 – 1545
Establishment of the HKU Phase 1 Clinical Trials Centre Mr. Henry Yau,
Managing Director, Clinical Trials Centre, The University of Hong Kong
1545 – 1615
Practical Experience in Phase 1 Clinical Trials Centre Operation in New Zealand Dr. Cheung-Tak Hung,
Managing Director, Zenith Technology
1615 – 1645
Phase 1 Clinical Trials in Mainland China: Opportunities and Challenges Dr. David Yang,
Chief Executive Officer, MicroConstants China
1645 – 1715
A Quality Auditor's Observations of QI and QA Lapses in Oversight of Early Phase Clinical Trials in Asia Dr. Chun-Han Ngim,
Director of Quality Assurance and Legal Affairs,
Regional Clinical Trial Center, Dong-A University Hospital

1715 – 1730
Summary and Closing Remarks Professor Yu-Lung Lau,
Chief Director, Clinical Trials Centre, The University of Hong Kong