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Clinical Trials in the USA / NCT06172374
Active, not recruiting Observational

A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials

NCT06172374 · tracked via the Priya Life Science USA tracker
Sponsor
ReCode Therapeutics
Phase
Observational
Started
2023-08-31
Last updated
2025-05-11

Condition(s) studied

Primary Ciliary Dyskinesia

Investigational drug(s) / intervention(s)

Sano Genetics Testing Kit

Sano Genetics Testing Kit: Genetic testing spit collection tubes for DNA testing

Study summary

Primary purpose is to identify individuals who have PCD due to a genetic mutation within the DNAI1 and other genes of interest to help refer participants to future clinical studies for this rare disease.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Participant must be at least 18 years old. 2. Participant must have a prior diagnosis of PCD or be deemed eligible upon completion of the PCD-enrichment screening questionnaire. 3. Participant must be under the care of an HCP for their PCD or symptoms potentially related to PCD. 4. Participant must be able to read, write, and understand English, and reside in a country where the shipment of biological samples is allowed. 5. Participant must be willing to be tested for genes involved in PCD. 6. Participant must be willing to be notified of eligibility for clinical studies (if appropriate) Exclusion Criteria: In ability to meet any of the inclusion criteria

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
ReCode Therapeutics, Inc. Menlo Park California

More ReCode Therapeutics trials in the USA

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06172374 on ClinicalTrials.gov ↗ ← All trials in the USA