NCT06478706CompletedPhase 2
A Two-Part Study to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetics of Repeat Doses of Inhaled ETD001 in People With Cystic Fibrosis
A Randomised, Double-Blind, Placebo Controlled, Two-Part Study to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetics of a Repeat Dose of Inhaled ETD001 in People With Cystic Fibrosis
Source: ClinicalTrials.gov · Last updated 28 Nov 2025
Brief summary (registry, in English)
This study is the first to give ETD001 to people with CF. The study will be run in two parts. Part A will assess if ETD001 is safe to give to people with CF, and Part B will assess if ETD001 improves lung function. The study drug is taken twice a day, in Part A it is taken for 7 days and in Part B for 28 days. In Part B there will be a separate period where dummy medicine is given for 28 days so the treatments can be compared. In Part A participants will receive 13 doses of either ETD001 or placebo, 8 people will take part. Participants will take up to 56 days to finish the study and make 5 outpatient visits. In Part B participants will receive 55 doses of ETD001 and 55 doses of placebo, 32 people will take part. Participants will take up to 140 days to finish the study and will make 8 outpatient visits. Study assessments include physical examinations, vital signs, heart traces, blood/urine samples, breathing tests and health questionnaires.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 57 (actual)
- First submitted
- 18 Jun 2024
- Start date
- 26 Jun 2024
- Primary completion date
- 14 Nov 2025
- Lead sponsor
- Enterprise Therapeutics Ltd
- Diseases
- Cystic fibrosis
- NCT number
- NCT06478706
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 57
- From 26 Jun 2024 to the primary completion date, 14 Nov 2025
- 21 sites in 4 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Received CFTR modulator therapy in the 60 days before screening
- Changes in bronchodilator, corticosteroid or other anti-inflammatory medications 14 days before screening
- Started dornase alfa, hypertonic saline, or other airway clearing therapy less than 28 days before screening
- Taking oral corticosteroids in excess of 10 mg/day or 20 mg every other day within 14 days of screening
- Use of diuretics, or renin-angiotensin aldosterone system antihypertensive drugs , drospirenone, or trimethoprim in the 28 days before screening
Other illness
- History of solid organ transplant
- Chest x-ray within the past 12 months with abnormalities suggesting unstable pulmonary disease other than CF
Other
- Abnormal liver function
- Abnormal renal function
- Unable to withhold use of long-acting bronchodilators 24 hours or short-acting bronchodilators 6 hours before spirometry assessments
- Unable to withhold use of anti-cholinergics within 24 hours of spirometry
- Using inhaled antibiotics for less than 2 complete cycles and unable to complete the entire study during the off or on cycle.
- Changes in inhaled or oral antibiotic use within 14 days of screening
- Presence of co-morbidities and medical history in the opinion of the investigator, may pose additional risk by participating in the study, or may confound the results of the study
Who the study is looking for
- Male \& female ≥ 18 years of age, who fit one of the following criteria:
- Women of childbearing potential using permitted contraception a minimum of 28 days before dosing until completion of the final follow up visit; Women of non-childbearing potential; Men using contraception from the time of the first dose, until completion of the final follow up visit;
- Confirmed diagnosis of CF
- FEV1 ≥ 40% and ≤ 90% of predicted normal for age, gender, and height
- Able to reproducibly perform spirometry manoeuvres
- Clinically stable CF lung disease
- Routine CF therapy has not changed within 28 days prior to screening.
- Provided written informed consent.
- Body mass index (BMI) \> 16 and \< 30 kg/m2
Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers
Sites (21)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Charité Universtaetsmedizin Coordinator of this site? Confirm its status | Berlin | Germany | Unknown status |
| CF-Studienzentrum Universitätsklinikum Köln Coordinator of this site? Confirm its status | Cologne | Germany | Unknown status |
| Westdeutsches Lungenzentrum am Universitätsklinikum Coordinator of this site? Confirm its status | Essen | Germany | Unknown status |
| IKF Pneumologie Coordinator of this site? Confirm its status | Frankfurt | Germany | Unknown status |
| Universitätsklinikum Frankfurt Coordinator of this site? Confirm its status | Frankfurt | Germany | Unknown status |
| LMU Kinikum Coordinator of this site? Confirm its status | Munich | Germany | Unknown status |
| Hospices Civils de Lyon Coordinator of this site? Confirm its status | Lyon | France | Unknown status |
| CHU de Montpellier Coordinator of this site? Confirm its status | Montpellier | France | Unknown status |
| Hôpital Cochin Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Hôpitaux de Toulouse Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
| Belfast Health and Social Care Trust Coordinator of this site? Confirm its status | Belfast | United Kingdom | Unknown status |
| Royal Papworth Hospital Coordinator of this site? Confirm its status | Cambridge | United Kingdom | Unknown status |
| All Wales Adult CF Centre Coordinator of this site? Confirm its status | Cardiff | United Kingdom | Unknown status |
| Queen Elizabeth University Hospital West of Scotland CF Service Coordinator of this site? Confirm its status | Glasgow | United Kingdom | Unknown status |
| Royal Brompton Hospital Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| Southampton General Hospital Coordinator of this site? Confirm its status | Southampton | United Kingdom | Unknown status |
| Azienda Ospedaliera Universitaria Meyer Coordinator of this site? Confirm its status | Florence | Italy | Unknown status |
| IRCCS Istituto Giannina Gaslini Coordinator of this site? Confirm its status | Genova | Italy | Unknown status |
| Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
| Ospedale Pediatrico Bambino Gesù Coordinator of this site? Confirm its status | Roma | Italy | Unknown status |
| Azienda Ospedaliera Universitaria Integrata Verona Coordinator of this site? Confirm its status | Verona | Italy | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.