person

Urh G.

Country
Slovenia
Department
#2250:Department of Endocrinology, Diabetes and Metabolic Diseases

Research Overview

Data & Insights

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Primary Speciality
Main therapeutic area

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Return Partnerships
Recurring site collaborations
10
Sites with multiple studies

Has run more than one trial at 10 of 38 partner sites.

Specializations

Metabolic Disorders

This investigator specializes in treating phenylketonuria (PKU), a rare inherited metabolic disorder that affects the body's ability to process phenylalanine. Their research encompasses innovative therapeutic approaches for managing this condition in patients aged 2 years and older.

  • Phenylketonuria Management
  • Blood Phenylalanine Level Control
  • Dietary Protein Optimization

The investigator focuses on evaluating novel treatment options to improve the quality of life for individuals affected by PKU.

Lipid Disorders

The investigator has expertise in treating familial hypercholesterolemia, including both heterozygous (HeFH) and homozygous (HoFH) forms. Their work involves exploring long-term therapeutic solutions for managing these inherited cholesterol disorders.

  • Familial Hypercholesterolemia Treatment
  • Cholesterol Management
  • Genetic Lipid Disorders

Their research extends to evaluating innovative treatments for patients with inherited cholesterol disorders.

Therapeutic Innovation

The investigator's work encompasses the development and evaluation of novel therapeutic compounds for genetic metabolic conditions. Their research focuses on investigating new treatment options for rare inherited disorders.

  • Long-term Safety Assessment
  • Treatment Tolerability
  • Therapeutic Efficacy

A key focus is placed on evaluating the safety and effectiveness of new therapeutic approaches for metabolic disorders.

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