Philip Stewart Low

West Lafayette, IN, United States of America

Philip Stewart Low

This inventor holds 111 USPTO granted patents and 83 published patent applications, plus 8 CIPO patents and 29 EPO patents, primarily in Targeted Drug Delivery (CPC class A61K49-0052). Top assignees: Purdue Research Foundation, Endocyte, Inc., Seattle Children's Hospital. Active years: 1992-2026.

IDiyas Innovation Intelligence. (2026). Inventor Profile: Philip Stewart Low. Retrieved from https://idiyas.com/inventor/philip-stewart-low

Data source: USPTO (United States Patent and Trademark Office) public patent records. Weekly synchronization. How IDiyas builds this profile

USPTO Granted Patents = 111 

% Patents Active = 92.8

 

 

Average Co-Inventor Count = 2.6

ph-index = 21

Forward Citations = 1,659(Granted Patents)

Forward Citations (Not Self Cited) = 1,129(Dec 10, 2025)


Inventors with similar research interests:


Location History:

  • Glenview, IL (US) (2012)
  • West Lafayetter, IN (US) (2014)
  • West Lafayette, IN (US) (1992 - 2024)

Company Filing History:


Years Active: 1992-2026

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Areas of Expertise:
Targeted Drug Delivery
CAR-T Cell Therapy
Imaging Agents
Lipid-Conjugates
Tumor Imaging
PSMA Ligands
Fibroblast Activation Protein
Bone Fracture Repair
Cholecystokinin B Receptor
Nanoparticle Mapping
Erythrocyte Band 3 Inhibitors
Folate Receptor Conjugates
111 patents (USPTO):Explore Patents

Title: **The Innovative Journey of Philip Stewart Low**

Introduction

Philip Stewart Low, based in West Lafayette, IN (US), is a distinguished inventor with an impressive portfolio of around 100 patents. Renowned for his work in drug delivery systems, Low's advancements have greatly contributed to the field of cell therapy and fracture repair, showcasing his significant role in the intersection of science and innovation.

Latest Patents

Among his latest groundbreaking patents is a platform titled "Targeted Ligand-Payload Based Drug Delivery for Cell Therapy." This innovative drug delivery system allows for a flexible fine-tuning of cell therapies by using an engineered fusion protein that is coupled with a high-affinity ligand. This ligand carries a payload of drugs that can be internalized by transplanted cells, thus enabling researchers to observe or manage the effects of transplanted cell therapy more effectively.

Another remarkable patent is "Targeting Anabolic Drugs for Accelerated Fracture Repair." This invention pertains to the targeted delivery of growth factors, vasoactive peptides, and other anabolic peptide drugs to bone fractures, facilitating accelerated healing. This targeted approach emphasizes Low's commitment to advancing therapeutic methods to enhance patient outcomes.

Career Highlights

Philip Stewart Low has made notable contributions while working with various esteemed organizations. He has been part of the Purdue Research Foundation, where he likely engaged in significant research and technological development. Additionally, his tenure at Endocyte, Inc. highlights his involvement with a firm focused on developing advanced therapies, particularly in the realm of personalized medicine.

Collaborations

Throughout his innovative career, Low has collaborated with distinguished colleagues such as Sumith A Kularatne and Christopher Paul Leamon. These partnerships have not only contributed to the success of various projects but have also fostered an environment of shared knowledge and breakthrough ideas.

Conclusion

In conclusion, Philip Stewart Low's extensive patent portfolio and collaborative efforts underscore his pivotal role as an inventor in the fields of drug delivery and therapeutic innovation. His work continues to inspire and lead advancements that may significantly improve medical treatments, demonstrating the importance of creativity and technology in enhancing human health.

Profile summary based on public USPTO records.
Data Sources: USPTO Patent Grant XML, Patent Center, EPO & CIPO • Normalized by IDiyas Innovation Graph. Methodology & provenance architecturePlease report any incorrect information to [email protected]
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