Bad Toelz, Germany

Verena Lutz

USPTO Granted Patents = 2 

Average Co-Inventor Count = 4.8

ph-index = 1

Forward Citations = 2(Granted Patents)


Location History:

  • Munich, DE (2010)
  • Bad Toelz, DE (2015)

Company Filing History:


Years Active: 2010-2015

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2 patents (USPTO):Explore Patents

Title: Verena Lutz: Innovator in Cancer Treatment Biomarkers

Introduction

Verena Lutz is a prominent inventor based in Bad Toelz, Germany. She has made significant contributions to the field of cancer treatment through her innovative research and patented inventions. With a total of 2 patents, her work focuses on improving the efficacy of cancer therapies.

Latest Patents

One of her latest patents is titled "Predictive marker for EGFR inhibitor treatment." This invention provides a biomarker that predicts the clinical benefit of EGFR inhibitor treatment in cancer patients. Another notable patent is "Determination of responders to chemotherapy." This invention relates to a method for determining whether a biological sample containing human lung cancer cells is sensitive to a combination of an epidermal growth factor receptor inhibitor and a chemotherapeutic agent. It involves assessing the overexpression of phosphorylated AKT and/or MAPK proteins in the biological sample.

Career Highlights

Verena Lutz is currently associated with Hoffmann-La Roche Inc., where she continues her research and development efforts. Her work has been instrumental in advancing the understanding of cancer treatment and improving patient outcomes.

Collaborations

Throughout her career, Verena has collaborated with notable colleagues, including Ulrich Brennscheidt and Otmar Herrgott, who serves as the Legal Representative. These collaborations have enhanced her research and contributed to the success of her inventions.

Conclusion

Verena Lutz is a trailblazer in the field of cancer treatment, with her innovative patents paving the way for more effective therapies. Her dedication to improving patient care through scientific research is commendable.

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