This is a demonstration / proof of concept not affiliated with Glycomine

Clinical Trial Eligibility Checker

Find out if you or your loved one may qualify for Glycomine-sponsored clinical trials for rare genetic diseases.

How It Works

1

Answer a Few Questions

Provide information about age, diagnosis, symptoms, and genetic testing status.

2

Get Your Results

Receive a preliminary eligibility assessment based on your answers.

3

Connect with Our Team

If potentially eligible, speak with our research team to learn more about next steps.

Family with child
Child

About Glycomine Clinical Trials

Glycomine is developing replacement therapies for rare genetic diseases with the goal of delivering meaningful improvements in quality of life for patients, caregivers, and families.

NGLY1 Deficiency

Clinical trials for patients with confirmed genetic diagnosis of NGLY1 deficiency.

PGAP3 Deficiency

Research studies for patients with confirmed PGAP3 genetic mutations.

Other Rare Diseases

Upcoming trials for additional ultra-rare genetic disorders.

Parent with child

About Glycomine

Glycomine is developing replacement therapies for rare genetic diseases with the goal of delivering meaningful improvements in quality of life for patients, caregivers, and families.

Our mission is to become the leading company in developing treatments for rare diseases by focusing on the underlying causes and addressing the most challenging symptoms.

Our Focus

  • Developing novel therapies for ultra-rare genetic disorders
  • Conducting rigorous clinical trials to ensure safety and efficacy
  • Supporting patients and families throughout their journey
  • Advancing scientific understanding of rare genetic diseases