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A Research Study to Advance the CF Therapeutics Pipeline for People Without Modulators

Join a CF study to explore new treatments for non-modulator patients.

Recruiting
12 years and older
All
Phase N/A

This study is for people with cystic fibrosis (CF) who do not use CF transmembrane conductance regulator (CFTR) modulators. CF is a genetic disorder that affects the lungs and other organs. CFTR modulators are medications that help some people with CF, but not everyone can use them. The REACH study aims to collect health data and samples from these individuals to help develop new treatments and improve research for those who can't use CFTR modulators.

Participation involves regular visits and data collection over 12 months. You must be at least 12 years old and not pregnant. You should not have used CFTR modulators or participated in other drug trials recently.

  • The study lasts for 12 months, requiring regular visits.
  • Participants must be willing to follow study procedures and visit schedules.
  • Eligibility includes not using CFTR modulators or investigational drugs recently.
Study details
    Cystic Fibrosis

NCT06504589

Nicole Hamblett

25 July 2026

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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