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Avidity Biosciences, Inc., San Diego, California: Arthur A. Levin, PhD, Chief Scientific Officer

Company: Avidity Biosciences, Inc., San Diego, CA
Nomination Submitted by: Berry & Company PR
Company Description: Avidity's mission is to profoundly improve people's lives by delivering a new class of RNA therapeutics. Our proprietary AOC™ platform is designed to combine the specificity of monoclonal antibodies with the precision of oligonucleotide therapies to better target underlying genetic drivers of diseases. Avidity's advancing and expanding pipeline currently includes three clinical-stage programs.
Nomination Category: Management Categories
Nomination Sub Category: Lifetime Achievement Award - Consumer Products Industries
2023 Stevie Winner Nomination Title: Arthur A. Levin, PhD, Chief Scientific Officer
  1. If you are providing an essay of up to 650 words, place it in this space:

    Total 576 words used.

    I would like to nominate Arthur A. Levin, Ph.D., chief scientific officer at Avidity Biosciences. He has more than three decades of experience in all aspects of drug development from discovery through drug registration, both in large pharmaceutical and biotechnology companies. Art has been instrumental in leading the development and advancement of Avidity’s proprietary Antibody Oligonucleotide Conjugates (AOC™) platform and has contributed to the significant progress Avidity has made in advancing its drug development programs.

    In the last 14 months, Art has helped lead the company in advancing three programs for three distinct rare diseases into clinical development for myotonic dystrophy type 1 (DM1), facioscapulohumeral muscular dystrophy (FSHD) and Duchenne muscular dystrophy mutations amenable to exon 44 skipping (DMD44). Avidity recently demonstrated for the first-time ever the successful targeted delivery of RNA into muscle, representing a revolutionary advancement for the field of RNA therapeutics. Results were based on a preliminary assessment of the Phase 1/2 MARINA™ clinical trial of AOC 1001, Avidity's lead clinical program leveraging its AOC platform, in adults with DM1. The AOC platform combines the specificity of monoclonal antibodies and the precision of oligonucleotide therapeutics, allowing for the delivery of RNA therapy to previously inaccessible tissue and cell types.

    Through Art’s research, he has been able to overcome a primary challenge with RNA therapeutics that has eluded scientists for decades – delivery of RNA molecules to cells outside the liver – and given the scientific community the first glimmer of hope in enabling these therapeutics to realize their true potential. Art is leading his team in expanding the reach of AOCs to target other tissue types in addition to muscle including cardiac tissue and immune cells to treat other diseases where patients have no approved therapies and there is a significant unmet need.

    Art is a pioneer in the field of RNA, antisense, and oligonucleotide therapeutics and he has played key roles in the development of numerous oligonucleotide therapies, including the first approved antisense drugs and the first microRNA-targeted therapeutic to enter clinical trials. As an advisor to executives in the pharmaceutical, biotechnology and venture capital communities, he has been able to assist in the growth and development of companies such as Ionis, Alnylam, Stoke, ProQR, Atalanta, Cardior, and others. As a result, he has contributed to the growth of oligonucleotide therapeutics companies and the development of drugs for important diseases, thus extending the reach and therapeutic importance of the technology.

    Art has served as a director of the Oligonucleotide Therapeutics Society and holds several additional scientific organization affiliations and honors. He received a doctorate in toxicology from the University of Rochester and a bachelor's degree in biology from Muhlenberg College. Art has more than 60 scientific articles and several of the most cited reviews in the field. His dedication to bring much needed therapies where there is an unmet need has helped usher in a new era for RNA therapeutics where we can potentially treat a broader range of diseases and has ultimately inspired a new generation of scientists in the field.

    Art’s lasting impact is not only due to his contributions to the RNA field and impressive resume but also the time and dedication he puts into training the next generation of scientists and innovators. His commitment, persistence and expertise in the pharmaceutical and biotechnology sectors is a huge inspiration for the team at Avidity and other researchers and drug developers and will continue to inspire in the years ahead.

  2. Which will you provide for your nomination in this category, an essay of up to 650 words describing the achievements of the nominee, OR a video of up to five (5) minutes in length describing the same? CHOOSE ONE:
    An essay of up to 650 words
  3. If you are submitting a video of up to five (5) minutes in length, provide the URL of the nominated video here, OR attach it to your entry via the "Add Attachments, Videos, or Links to This Entry" link above, through which you may also upload a copy of your video:

     

  4. In bullet-list form, provide a brief summary of up to ten (10) of the chief accomplishments over the career of the nominee. This is required whether you are submitting a video or an essay:
    1. Art led the development of Vitravene (fomivirsen), the first antisense drug approved by the FDA (in 1998), in his prior role as senior vice president of drug development at Ionis (formerly Isis) Pharmaceuticals.
    2. Led the development of miravirsen (SPC3649), the first microRNA-targeted antisense oligonucleotide (ASO) therapeutic to enter clinical trials (in 2012), in his prior role as chief development officer at Santaris Pharma.
    3. Led the development of Avidity Biosciences’ (Avidity) Antibody Oligonucleotide Conjugates (AOC™) platform entirely in-house through years of engineering and optimization of each component, resulting in a pipeline of therapies for severe rare muscle diseases and broadening the potential scope of RNA-targeted therapies.
    4. Led the team at Avidity in demonstrating for the first-time ever the successful targeted delivery of RNA into muscle, revolutionizing the field of RNA therapeutics, in December 2022.
    5. Art has published more than 60 scientific articles and several of the most cited reviews in the field.
    6. He has been recognized by many industry awards including FiercePharma’s Most Influential People in Biopharma, Global Genes’ RARE Champion of Hope Award, and Biotech Week Boston’s Lifetime Luminary Award in 2022 alone.
    7. Has served on the scientific advisory boards or as a member of board of directors for multiple institutions including Ionis Pharmaceuticals, Alnylam Pharmaceuticals, Stoke Therapeutics, ProQR Therapeutics, Atalanta Therapeutics, Cardior Pharmaceuticals, and others.
    8. Has served as a director of the Oligonucleotide Therapeutics Society and holds several additional scientific organization affiliations and honors.
Attachments/Videos/Links:
Arthur A. Levin, PhD, Chief Scientific Officer
URL Avidity Announces Positive AOC 1001 Phase 1/2 MARINA™ Data Demonstrating First-Ever Successful Targeted Delivery of RNA to Muscle - Revolutionary Advancement for the Field of RNA Therapeutics
URL Most influential people in biopharma—the scientists
URL AAN 2022 | AOCs: future outlooks in other disease areas
URL #JPM21: Avidity CSO Art Levin runs full speed to the clinic with 'dream' antibody oligonucleotide conjugate therapy
URL Treating Disease at the RNA Level with Oligonucleotides
URL Targeting Therapeutic Oligonucleotides