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Search / Trial NCT03269474

Computational Drug Repurposing for All EBS Cases

Launched by JOYCE TENG · Aug 30, 2017

Trial Information

Current as of June 06, 2025

Recruiting

Keywords

Epidermolysis Bullosa Genetic Expression Drug Repurposing Computational Approaches Drug Discovery

ClinConnect Summary

This clinical trial is studying a skin condition called Epidermolysis Bullosa (EB), which causes the skin to be very fragile and easily blistered. The researchers want to learn how the skin behaves differently in people with EB, especially between areas of skin that have blisters and those that do not. They will be using advanced computer techniques to find existing medications that could help improve wound healing and reduce pain for all types of EB. The exciting part is that the medications they are looking at have already been approved for other uses, which means they could be repurposed for EB patients more quickly and affordably than developing new drugs from scratch.

Anyone of any age diagnosed with EB or healthy individuals without EB can participate in the study, as long as they can attend study visits for tissue and blood sample collection. However, people who are pregnant, breastfeeding, or have serious health issues that could affect their safety or the study will not be included. Participants can expect to contribute to important research that may lead to better treatments and an improved quality of life for those suffering from this condition.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Subjects of all ages
  • Diagnosis of all subtypes of EB subjects
  • Healthy, non-EB subjects
  • Ability to complete study visit to collect tissue and blood specimen
  • Exclusion Criteria:
  • Pregnancy, breast feeding
  • Prior history of liver disease
  • Serious known concurrent medical illness or infection, which could potentially present a safety risk and/or prevent tissue collection from subjects

About Joyce Teng

Joyce Teng is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative clinical studies. With a focus on enhancing therapeutic strategies across various medical fields, Joyce Teng collaborates with leading researchers and institutions to design and implement rigorous trials that adhere to the highest ethical and scientific standards. The organization prioritizes participant safety and data integrity while fostering an environment of transparency and collaboration. By leveraging cutting-edge methodologies and a patient-centered approach, Joyce Teng aims to contribute significantly to the development of effective treatments and therapies that address unmet medical needs.

Locations

Palo Alto, California, United States

Patients applied

0 patients applied

Trial Officials

Joyce M Teng, MD, PhD

Principal Investigator

Stanford University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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