Condition
Rare Disorders clinical trials and research
As of November 12, 2026, Find a Trial lists 6 Rare Disorders clinical trials that are recruiting, at sites in 4 countries (most in United States (3), Austria (1), South Korea (1)). Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 6Clinical trials
- 4Countries
Newest Rare Disorders clinical trials
| Study | Phase | Where | Status | Registered |
|---|---|---|---|---|
| Transitioning to Adult Care for Kids with Rare Endocrine Disorders | — | Daegu and 10 other locations | Recruiting | Aug 25, 2026 |
| AI-assisted Rare-Disease Diagnosis | — | Cangzhou and 11 other locations | Recruiting | Jun 16, 2026 |
| Psychoeducational program for children with rare diseases | — | Graz, Austria and 6 other locations | Recruiting | Dec 11, 2024 |
| Gene discovery for rare and undiagnosed genetic conditions | — | Boston, Massachusetts | Recruiting | Apr 19, 2016 |
| Registry for patients with rare diseases | — | Sioux Falls, South Dakota | Recruiting | Feb 15, 2013 |
| Using genome sequencing to discover genetic causes of rare disorders | — | Bethesda, Maryland | Recruiting | Mar 16, 2010 |
All recruiting trials (6)
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Transitioning to Adult Care for Kids with Rare Endocrine Disorders
We’re testing a structured transition program to help young adults move from pediatric to adult endocrine care and see if it improves staying in care and quality of life.
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AI-assisted Rare-Disease Diagnosis
A multicenter randomized test to see if an AI diagnostic tool can help doctors make faster, more accurate rare-disease diagnoses for patients with unresolved symptoms.
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Psychoeducational program for children with rare diseases
This study is testing a new educational program to see if it helps children with rare diseases understand their condition better and feel happier.
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Gene discovery for rare and undiagnosed genetic conditions
This study is trying to find the genetic causes of rare and undiagnosed conditions by collecting DNA and medical information from affected families to improve diagnosis and treatment options.
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Registry for patients with rare diseases
This study is creating a central registry for people with rare diseases to help connect them with researchers and improve treatments.
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Using genome sequencing to discover genetic causes of rare disorders
This study is testing if using genome sequencing can help find the genetic causes of rare inherited diseases for people who currently have no answers about their conditions.
Related topics
Quick answers
How many Rare Disorders clinical trials are recruiting right now?
6, as of November 12, 2026. We update this list each time we refresh our data from ClinicalTrials.gov.
Where are these trials running?
In 4 countries. The most sites are in United States (3 trials), Austria (1 trial), South Korea (1 trial), China (1 trial). Each study page lists its sites and which ones are recruiting.
How do I join one?
Open a study, check the "Is this trial a fit for you?" section, then contact the study team listed on the page. They will ask a few screening questions. Asking is free and does not commit you to anything. Talk it over with your doctor first.
Find the studies that fit you
A list is a starting point. Tell us your situation in your own words and we'll rank the studies that match and explain why. It's free and needs no account.