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Could your cells hold the key to a new CF treatment?

NCT ID NCT03161808

First seen Feb 02, 2026 · Last updated Jun 13, 2026 · Updated 18 times

Summary

This study collects blood, nasal, and intestinal cells from 500 people with cystic fibrosis (CF) who have rare gene mutations. These cells are stored and shared with researchers to test potential new drugs in the lab. The goal is to find treatments that work for people whose rare mutations are not covered by current therapies.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • University of Alabama at Birmingham

    RECRUITING

    Birmingham, Alabama, 35233, United States

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact Phone: •••-•••-•••• Email: •••••@•••••

Conditions

The condition(s) this trial relates to.

cystic fibrosis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.