Cystic Fibrosis Clinical Trial Landscape

A daily email digest covering new and updated cystic fibrosis clinical trials from ClinicalTrials.gov. Track CFTR modulator combinations, gene therapy approaches, CF complications programs, and next-generation therapies targeting the 10% not covered by current modulators.

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Why cystic fibrosis trial monitoring matters in 2026

Cystic fibrosis is one of the most commercially significant rare disease therapeutic areas. The CFTR modulator revolution — led by elexacaftor/tezacaftor/ivacaftor (Trikafta/Kaftrio) — has transformed outcomes for the approximately 90% of CF patients with at least one F508del allele. But the remaining 10% of patients with rare mutations, plus the long-term question of whether modulators can fully prevent disease progression, means an active and commercially important pipeline continues.

Key signals in the CF pipeline for 2026 and beyond:

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What DataLookout monitors for cystic fibrosis

Configure your profile with condition and mechanism keywords to match your intelligence needs:

What DataLookout adds to ClinicalTrials.gov

ClinicalTrials.gov RSS feeds tell you that a study record was updated. DataLookout compares each record against the previous day across 13 tracked fields and tells you which one changed, with the old and new values, for every Cystic Fibrosis trial on your watchlist. Each change is classified as critical, notable, or minor, so a trial flipping from recruiting to suspended does not read the same as a contact-details edit.

Who uses cystic fibrosis trial monitoring

Rare disease pharma BD and strategy teams

Companies active in CF — or seeking to enter the space — track new trial registrations to identify partnership opportunities and anticipate competitive challenges. With Vertex dominating the CFTR modulator market, the strategic questions center on whether gene therapy approaches can achieve the efficacy needed to displace highly effective modulators, and what the commercial opportunity looks like for the remaining unaddressed patient population.

CF-focused biotech analysts and investors

Investors covering rare pulmonary disease use trial registrations as pipeline intelligence. Gene therapy programs advancing into Phase 2 in CF represent significant capital events, and monitoring new trial activity allows analysts to track pipeline maturation ahead of major data readouts.

Cystic Fibrosis Foundation and patient advocacy networks

The CFF and patient advocacy organizations actively fund and monitor the CF research pipeline. Real-time awareness of new trial registrations enables advocates to connect patients — particularly those with rare mutations not addressable by current modulators — with appropriate clinical study opportunities.

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Frequently asked questions

How current is the cystic fibrosis trial data?

Our pipeline fetches from ClinicalTrials.gov every morning. Studies posted or updated in the preceding 24 hours appear in that day's digest. ClinicalTrials.gov is updated as sponsors register new trials or submit protocol amendments.

Can I track CFTR modulator and gene therapy trials separately?

Yes. On the Pro plan ($149/month), you can create multiple search profiles — for example, one monitoring CFTR modulator programs and another tracking gene therapy and mRNA approaches in CF — each delivering a focused daily digest.

Does DataLookout cover CF complications trials?

Yes. Adding keywords like "CF-related diabetes", "cystic fibrosis liver disease", or "CF bone disease" will surface trials targeting specific complications of cystic fibrosis alongside or separate from primary CFTR-targeting programs.

Does DataLookout cover pediatric CF trials?

Yes — pediatric dosing, safety, and efficacy studies registered on ClinicalTrials.gov are included. As CFTR modulators expand to younger age groups, tracking the associated clinical program is important for the field.

Live trial data Data as of 2026-09-16, ClinicalTrials.gov

198 active trials, 120 recruiting.

Industry sponsors run 23 of these trials. The rest are run by universities, hospitals, government bodies and other non-commercial sponsors. The table below lists the 5 largest of 15.

View the full Cystic Fibrosis pipeline on the dashboard

Notable trials Ranked by recent tracked changes, ClinicalTrials.gov data as of 2026-09-16
TrialStatusLatest tracked changeSeen
Pharmacokinetics of Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis NCT07809867Not Yet RecruitingPrimary endpoint(s) modified2026-09-15
Real World Clinical Outcomes With Novel Modulator Therapy Combinations in… NCT04602468Active, Not RecruitingInterventions modified2026-09-10
A Phase 2 Study Evaluating Safety and Tolerability of RCT2100 (CFTR mRNA) in… NCT06237335Active, Not RecruitingCompletion moved earlier: 2026-12-31 → 2026-112026-08-20
Pulmonary Vascular Disease in CF NCT04549077Active, Not RecruitingCompletion pushed: 2026-01-01 → 2027-01-012026-09-15
Hyperpolarized Imaging for New Treatments NCT04259970Active, Not RecruitingCompletion pushed: 2026-12-31 → 2027-05-012026-09-15

Each trial page shows every change DataLookout has recorded for that trial.

Track these trials with DataLookout

DataLookout checks ClinicalTrials.gov every day and records what changed on each trial: status, enrollment, phase, primary endpoint, completion dates, sites, sponsor, and the stated reason a trial stopped. Add a sponsor or a disease to your watchlist, or save any search, and the changes arrive in a daily or weekly email digest.

Free, $0 forever: 1 sponsor + 1 disease watchlist, 1 saved search in your email digest, track up to 5 individual trials, daily change detection, Trials at Risk (top trial). No credit card.

Starter, $49/month: 3 sponsor + 3 disease watchlists, 3 saved searches in your email digest, track up to 25 individual trials, full Trials at Risk list and landscape reports.

Pro, $149/month: unlimited sponsor and disease watchlists, unlimited saved searches, track unlimited individual trials, CSV export, priority email support.

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