CLOSE

Specials

I agree We use cookies on this website to enhance your user experience. By clicking any link on this page you are giving your consent for us to set cookies. More info

Skip to: Curated Story Group 1
Life Sciences Review
US
EUROPE
CANADA

About Us

Conference

Partner With Us

  • APAC
    • US
    • EUROPE
    • CANADA
    • LATAM
  • Drug Discovery
    Antibodies
    Bioinformatics & Genomics
    BioTech
    Cell and Gene Therapy
    Drug Discovery and Development
    Life Science AI
    Next-Generation Sequencing
    Therapeutics
  • Biomanufacturing
    Biomanufacturing
    CDMO
    Cosmetic
    CRO
    Life Science Testing And Compliance
    Supplement Manufacturing
  • Business Services
    Life Science Consulting
    Life Sciences Marketing and Communication
  • Leadership Perspectives
  • Innovation Insights
  • News
  • Magazines
×
#

Life Science Review Weekly Brief

Be first to read the latest tech news, Industry Leader's Insights, and CIO interviews of medium and large enterprises exclusively from Life Science Review

Subscribe

loading

Thank you for Subscribing to Life Science Review Weekly Brief

A featured contribution from Leadership Perspectives: a curated forum reserved for leaders nominated by our subscribers and vetted by our Life Sciences Review Advisory Board.

Inc.

Steven Cohen, Executive Director, Translational Medicine-Oncology & Internal Medicine, & Business Development-IM at Daiichi Sankyo

Life Sciences Review upon their request

Steven Cohen

There have been multiple ramifications of the COVID-19 pandemic for drug development. Some of these have been well-publicized, most notably the delay of clinical trials, which was largely due to the potential exposure of volunteers, patients, and staff to the virus. Additionally, thewidespread supply chain interruptions that are discussed frequently in the lay press also affected drugsand other clinical trialsupplies.


However,there is an area of drug development affected by the pandemic that has not received much attention.  That is the decrease in interaction among people in academia, biotech, and pharmathat has traditionally yielded substantial progressin target and drug discovery as well as in advancing compoundsthrough the various stages of development. 


There are respective diverse merits to universities, biotechs, and pharma where each may complement the other to enhance the various stages of R&D,from first-in-man studies, through proof of mechanism and proof of concept, and even later stages of development and post-registration trials. The relativeacademic freedom and small group structures intrinsic to universities and biotech may have advantages for a more streamlined process and quick decision-making, whether that is to further explore a novel mechanism or to terminate a project.Clearly though, once it is decided that a specific target or mechanism is worthy of further experimentation, the collaboration of academia, biotech, and pharmaisimportant to advancing a program expeditiously, with each site utilizing their respective strengths. For example, universities have excellent scientists, but typically turn to medicinal chemists, pharmacologists, and toxicologists working in pharma to further evaluate a compound. Additionally, pharma has more resources to invest in promising targets than most universities and small biotech companies. And if a compound is advanced to clinical trials, the translational medicine and clinical trialistsreadily available in pharma are experienced in testing these compounds for safety and efficacy.At all stages of drug discovery and development,the comprehensive and continual interactions among academia, biotech, and pharmaare critical to ensuremedicines are being discovered and developed appropriately to meet unmet medical needs.


An example at Daiichi SankyoCompany Ltd (DS), is our long-standing collaboration with Sanford Burnham Prebys in La Jolla, California. We initiallyentereda comprehensive alliance to develop first-in-class therapeutics for the treatment of cardiovascular-metabolic diseases. This was later extended to include rare diseases and oncology. The collaboration was based on an open-innovation modelto bridge the gap between target discovery and pre-clinical drug development.The focus was on studying new mechanisms of disease to identify, validate, and screen novel drug targets to address unmet medical needs worldwide. Sanford Burnham Prebys  identifiedand validated targets in collaboration with Daiichi Sankyo, after which collaborative teams conduct drug screening to identify compounds that modulated the targets using facilities at both sites. Scientists at Daiichi Sankyohave appreciated continued and expanded access to Sanford Burnham Prebys’ deep human biology insights and drug discovery technology, with the goal of advancing lead compounds toward clinical trials.


During the pandemic, due to respective quarantines in California and Tokyo, experiments were delayed at both partners’ sites leading to missed timelines on multiple occasions. However, due to the close, collaborative relationship that has developed over many years between our two groups, we were able to support each other.  Wecovered each other’s workloads as each respective labopened in the different regions, even if it was not a task initially allocated to that group. Additionally, there was also flexibility as to the allocation and utilization of the budget from one fiscal year to the next as some timelines were extended beyond the original plan.


From nearly the beginning of the pandemic, the traditional interaction among academia, biotech, and pharma was disturbed. One of the first major meetings cancelled was a key annual university tech transfer meeting for engaging organizations across multiple disciplines, followed by the Keystone conferences and numerous scientific, clinical, and business meetings.There was a near instantaneous collapse of the usual conferences that were relied on to publicize novel ideas and advance scientific knowledge and drug development.While technology became increasingly sophisticated in allowing meeting participants to interact virtually, this never approached the collegial, informal, intermingling that occurs when you happen to engage the person sitting next to you in a conversation about their work. In addition,at virtual scientific and medical conferences,one can no longer approach someone at their poster or after their talk.  These spontaneous personal interactions were all but eliminated.


Other interactions betweenacademia, biotech, and pharmabased upon mutual interest in a research or clinical project were either delayed or came to a halt. For example, something as simple as a material transfer agreement, which allows a compound to be transferred from a university or biotech to a pharma that is interested in reproducing data, may not have occurred since either or both labs may have been closed due to pandemic restrictions.These types of interruptions led to delays in starting collaborations and potentially extending the timeline for the entire drug development process.


In conclusion, one of the lessons for drug developers from this pandemic is the vital intersection of academia, biotech, and pharma have in producing medical therapies. Even though the ideal will probably always be in-person meetings, we need to be able to continually think of innovative ways of communicating and working together effectively to ensure that progress to develop safe and efficacious drugs to meet unmet medical needs is not delayed, even when extraneous forces do not allow us to communicate or allocate work as effectively as we would like. With the first mRNA vaccinesbeing made available during the pandemic inform us that the continued innovationcan occur even during a pandemic. It will be interesting to see how new advances in technology, such as the metaverse and artificial intelligence, may mitigate some of theseissues.  However,for the foreseeable future, in-person events and collaborations will continue to be the method of choice for advancing science into new medicines.


The articles from these contributors are based on their personal expertise and viewpoints, and do not necessarily reflect the opinions of their employers or affiliated organizations.
The Leadership Perspectives forum brings together voices shaping the future of life sciences. It features leaders who are advancing change across the industry through strategic leadership and applied insight.
EDITOR'S CHOICE
  • Willis Towers Watson

    ICON [NASDAQ: ICLR]

    The Significant Increase in Demand for Clinical Research Associates (CRAs)

    Helen Yeardley, Executive Vice President, ICON [NASDAQ: ICLR]

  • Willis Towers Watson

    PacBio [NASDAQ: PACB]

    The Talent - Culture Continuum: How to Manage an Innovation Culture Amid Growth and Change

    Alvin Hom, Head of Global Talent Acquisition, PacBio [NASDAQ: PACB]

  • Willis Towers Watson

    Repligen Corp [NASDAQ: RGEN]

    Gene Therapy-Therapeutic Viral Vectors; Manufacturing, Challenges, and Innovation

    Rachel Legmann, PhD, Senior Director of Technology, Gene Therapy, Repligen Corp

  • Willis Towers Watson

    Ionis Pharmaceuticals [NASDAQ: IONS]

    Bridging the Diversity Divide

    Victoria Sanjurjo, Medical Director, Clinical Development, Ionis Pharmaceuticals, Inc [NASDAQ: IONS]

Life Sciences Review APAC
Follow on LinkedIn

About

  • Home
  • About Us
  • Partner With Us

Stay Connected

  • Subscribe
  • Newsletter
  • Sitemap

Contact Us

  • editor@lifesciencesreview.com
  • sales@lifesciencesreview.com
  • marketing@lifesciencesreview.com

Legal

  • Editorial Policy
  • Privacy Policy
  • Terms of Use

© 2026 Life Sciences Review APAC. All rights reserved. Headquartered in Fort Lauderdale, FL, USA.

This content is copyright protected

However, if you would like to share the information in this article, you may use the link below:

https://www.lifesciencesreviewapac.com/leadership-perspective/life-sciences-review-upon-their-request-nwid-1270.html