GENE ONLINE|News &
Opinion
Blog

2020-07-23| PartnerAsia-Pacific

Part II Highlights of BIO Asia-Taiwan 2020 (Day 1): Global Trends in Biotech and the Impact of COVID-19

by Rajaneesh K. Gopinath
Share To

By Rajaneesh K.Gopinath & Ruchi Jhonsa

TAIPEI, TAIWAN – Day 1 of BIO Asia-Taiwan 2020 saw remarkable talks from eminent scientists who shared their cutting edge research and biotech professionals who discussed the impact of the COVID-19 on global biotech trends. In part 2, we put together selected takeaways from the day. Link to Part 1

Milasen and Prospects for Hyper-Personalized Medicine

Nearly 30 million patients are suffering from rare diseases in the United States without any therapeutic options. Despite the progress achieved in genetic testing technology, such diseases prove to be a significant challenge for drug developers.

Professor Timothy Yu, Principal Investigator and Attending Physician at Boston Children’s Hospital shared a remarkable case. Milasen, an antisense oligonucleotide (ASO)-based drug, was manufactured, and FDA approved rapidly to save a single patient suffering from a rare, lysosomal storage disorder. Dr. Yu and colleagues designed an oligonucleotide to treat a fatal neurodegenerative condition called Batten disease in a 6-year-old patient, Mila Makovec.

Milasen performed well in clinical evaluations by reducing epileptic events and did not exhibit any significant adverse reactions. In the beginning, the patient had 15 to 30 seizures a day, each lasting 1 to 2 minutes. Milasen reduced the frequency of seizures to 0-20 times a day and decreased the duration of each seizure to less than a minute. Following successful trials, several stakeholders, including drug manufacturers and the FDA raced to deliver the drug for Mila, setting a record in the timeline of drug development. By virtue of the positive trial data, the drug received FDA approval within just three months. Milasen is a pioneering example of personalized medicine and a model for other drug developers to emulate and seek approval for rare disease drugs.

 

Organoids to Model Human Disease

Prof. Hans Clevers, Principal Investigator at the Hubrecht Institute, enlightened the audience by mentioning that the concept of personalized medicine is not new. He proceeded to explain that the 60-year-old practice of performing an antibiotic resistance screen to administer the right antibiotic to a pneumonia patient is essentially “personalized medicine”. He then segued into the concept of organoids, the three-dimensional structures derived from stem cells, and their promise in advancing personalized medicine.

Professor Clevers pointed out that “the gut harbors the champion of all stem cells” since intestinal stem cells (ISCs) plays a crucial role in renewing cell populations. The harsh environment of the gut damages the intestinal epithelial lining, and therefore every 4-6 days, ISCs differentiate to help renew the population. Stem cell-derived mini-gut organoids grown in a dish could be successfully transplanted to cure patients suffering from inflammatory bowel disease (IBD).

Today, many organs can grow into organoids, and they can be derived from both healthy and disease tissues. This opens up multiple avenues for studying diseases and facilitates drug development. For instance, researchers could grow organoids from both cancer and healthy cells and perform various analyses, including sequencing, to identify cancer-causing mutations. Besides, cancer organoids serve as a wonderful platform for testing drug combinations, and a cancer organoid biobank can be established to achieve personalized medicine. Extensive research in this area has culminated in the launch of Hubrecht Organoid Technology (HUB), “a paradigm-shifting platform for drug discovery and development, companion diagnostics, and (pre)clinical patient stratification.”

In summary, Prof. Clevers described organoids as “patients in the lab” and reemphasized the merits of the organoid technology platform and the immense potential it holds in advancing different aspects of drug discovery.

 

Emerging from the Pandemic: A Global Perspective

Dr. Graham Lewis, Vice President, Global Pharma Strategy, IQVIA, presented a perspective on changes that will happen to the pharmaceutical industry and health care sector post-COVID.

During the pandemic, there is a growing demand for pharmaceutical companies to support health care systems, increasing net sales. However, Dr.Lewis reckons the overall sales would be threatened in the future due to an increase in rebates and discounts, price raises and market hurdles, and delays in revenue streams and clinical development. He forecasts a lower growth over the next few years, and net prices will transfer to virtually zero levels.

Companies will need to develop vaccines at the same time, ensuring that chronic conditions are managed effectively. This demands new ways of working. “There’s going to be a great need for more flexibility and efficiency in research and development. These methods, of course, have been available now for a number of years. But the industry has been slow to take them up. But because communication is moving pressingly into a digital or virtual framework, then the acceleration of skill sets and scale is going to be essential,” said Dr. Lewis. Post the pandemic, pharma companies will have to re-assess missions and their overall strategy to support health systems, accelerate digital transformation, build or strengthen capabilities to enable novel patient support programs, and re-evaluate everything from launching, resourcing models, deployment development, portfolio priorities, and supply chain.

Dr. Lewis opined that one interesting dimension of the changes that we are seeing is the gradual growing importance of BRICS nations, Brazil, Russia, India, and China. “China was already the second-largest pharmaceutical market in 2019. And we expected it to retain that position in 2022 and indeed beyond that as well. We do see Brazil, though, becoming more important. And our current estimates suggest that Brazil will be the fifth-largest pharmaceutical market by 2022. India will enter the top 10 for the first time, in our view, and Russia will be just below in 12th position.” he concluded.

Related Article: Part I Highlights of BIO Asia-Taiwan 2020 (Day 1): The Effect of COVID-19 on Global Biotech Industry

©www.geneonline.com All rights reserved. Collaborate with us: service@geneonlineasia.com
Related Post
FDA Requests for a $7.2 Billion Budget in FY 2025 for Critical Health Initiatives
2024-03-12
Wegovy Expands Its Reach: First Weight-Loss Medication Approved to Reduce Cardiovascular Risk
2024-03-11
FDA Boxed Warning for CAR-T therapy, Affecting Bristol-Myers Squibb, Novartis, Janssen, Gilead Sciences
2024-01-24
LATEST
WHO Raises Alarm: Bird Flu Threat to Humans an ‘Enormous Concern’
2024-04-19
The Legal Battlefield of Weight-Loss Drugs: Eli Lilly and Novo Nordisk on the Defensive
2024-04-18
Pharmacogenomics in Asia-Pacific: Nalagenetics CEO Levana Sani Offers Insights and Strategies
2024-04-17
Rice University Engineers Develop Miniature Brain Stimulator for Safer and Less-invasive Neuromodulation
2024-04-17
Breakthrough Screening Platform to Assess SARS-CoV-2 Mutations and Potential Treatments
2024-04-16
Join Us for the SABPA OC/LA 16th Annual Biomedical Forum!
2024-04-16
Sequencing Revolution Spotlights the Titans of NGS Innovation
2024-04-16
EVENT
2024-04-20
16th SABPA OC/LA Annual Biomedical Forum
The Beckman Center, 100 Academy, Irvine, CA, 92617
2024-04-27
2024 Biomedical Final Pitch Competition
Room DA1620, Dana Building, Dana-Farber Cancer Institute, 99 Jimmy Fund Way, Boston, MA 02115
Scroll to Top