Didcot, United Kingdom

Gary Nugent

USPTO Granted Patents = 2 

 


Average Co-Inventor Count = 9.0

ph-index = 2

Forward Citations = 11(Granted Patents)


Location History:

  • Didcot, GB (2013)
  • Sutton, GB (2013)

Company Filing History:


Years Active: 2013

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2 patents (USPTO):Explore Patents

Title: Gary Nugent: Innovator in Duchenne Muscular Dystrophy Treatment

Introduction

Gary Nugent is a prominent inventor based in Didcot, GB. He has made significant contributions to the field of medicine, particularly in the treatment of Duchenne muscular dystrophy. With a total of 2 patents to his name, Nugent's work is paving the way for innovative therapeutic solutions.

Latest Patents

Nugent's latest patents focus on the treatment of Duchenne muscular dystrophy. One of his notable inventions involves a compound of Formula (1), which includes various components that may represent N or CR, with a divalent group selected from O, S(O), and other elements. This compound is designed for the therapeutic and prophylactic treatment of Duchenne muscular dystrophy, Becker muscular dystrophy, or cachexia. Additionally, he has developed drug combinations that consist of one or more compounds of formula (1) with ancillary agents, aimed at enhancing the treatment efficacy for these conditions.

Career Highlights

Gary Nugent is currently associated with Summit Corporation Plc, where he continues to innovate in the pharmaceutical field. His work is characterized by a commitment to developing effective treatments for debilitating diseases, showcasing his dedication to improving patient outcomes.

Collaborations

Nugent collaborates with esteemed colleagues such as Graham Michael Wynne and Stephen Paul Wren. Their combined expertise contributes to the advancement of research and development in the medical field.

Conclusion

In summary, Gary Nugent is a dedicated inventor whose work in the treatment of Duchenne muscular dystrophy is making a significant impact. His innovative patents and collaborations reflect his commitment to advancing medical science and improving the lives of those affected by muscular dystrophies.

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