Glenside, PA, United States of America

B Wesley Trotter

USPTO Granted Patents = 29 

 

Average Co-Inventor Count = 5.0

ph-index = 2

Forward Citations = 39(Granted Patents)


Location History:

  • Glenside, NJ (US) (2010)
  • Newton Highland, MA (US) (2013)
  • Newton Highlands, MA (US) (2013 - 2016)
  • Glenside, PA (US) (2008 - 2018)
  • Medfield, MA (US) (2014 - 2020)

Company Filing History:


Years Active: 2008-2020

where 'Filed Patents' based on already Granted Patents

29 patents (USPTO):

Title: Unveiling the Inventive Genius of B Wesley Trotter

Introduction:

In the realm of innovation and patent accomplishments, B Wesley Trotter stands as a beacon of creativity and success. Hailing from Glenside, PA, with an impressive portfolio of 29 patents, Trotter's contributions have made significant waves in the field of pharmacology.

Latest Patents:

Trotter's latest patents showcase his expertise and focus on pharmaceutical advancements. His creations, such as the Substituted Indazole Compounds and Heteroaryl Substituted Benzoic Acids as RORgammaT Inhibitors, highlight his commitment to developing treatments for RORgammaT-mediated diseases.

Career Highlights:

Having worked with renowned companies like Merck Sharp & Dohme Corporation and Merck & Company, Inc., Trotter has honed his skills and expertise in the pharmaceutical industry. His innovative approach and dedication to research have propelled him towards groundbreaking discoveries.

Collaborations:

Throughout his career, Trotter has collaborated with esteemed professionals in the field. Partnerships with individuals like Kausik K Nanda and Mark T Bilodeau have not only enriched his work but also led to the development of impactful solutions in pharmacology.

Conclusion:

In conclusion, B Wesley Trotter's journey as an inventor is a testament to his unwavering commitment to innovation and scientific advancement. His patents, collaborations, and career highlights underscore his invaluable contributions to the field of pharmaceutical research, shaping the landscape of RORgammaT-mediated disease treatments.

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