Cystic FibrosisPhase 2NCT06237335
A Phase 2 Study Evaluating Safety and Tolerability of RCT2100 (CFTR mRNA) in Healthy Participants and in Participants With CF
A Phase 2 study testing RCT2100 and Ivacaftor in people with Cystic Fibrosis, run by ReCode Therapeutics at 23 sites in 5 countries.
Trial summary
This is the first-in-human study with RCT2100 and is designed to provide safety and tolerability data for future clinical studies. Read more about this study
- Who is it for?
- Ages 18 to 60 yearsHealthy volunteers can take part
- Conditions the study is for
- Cystic Fibrosis
- What is being tested?
- RCT2100 and Ivacaftor
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 128 participants
- Where
- 23 sitesin 5 countries
- Study dates
- 1 Feb 2024to Nov 2026
- Phase
- Phase 2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- All sexes
- Healthy volunteers accepted
- Adult
Part 1 Major Inclusion Criteria:
- Healthy, adult, male or female, 18-55 years of age, inclusive, at screening.
- Body weight greater than or equal to 50 kg and body mass index (BMI) between 16-32 kg/m2, inclusive
- The participant has a forced expiratory volume in one second (FEV1) of at least 80% predicted
- The participant is considered by the investigator to be in good general health as determined by medical history, clinical laboratory test results, vital sign measurements, 12-lead ECG results, and physical examination findings at screening.
- Understands the study procedures in the informed consent form (ICF), and is willing and able to comply with the protocol.
Part 1 Major Exclusion Criteria:
- History or presence of clinically significant medical, surgical, clinical laboratory, or psychiatric condition or disease.
- The participant has supine blood pressure (BP) >150 mm Hg (systolic) or >90 mm Hg (diastolic), following at least 5 minutes of supine rest.
- The participant has abnormal clinical laboratory tests at screening, as assessed by the study-specific laboratory.
- The participant is a smoker or has used nicotine or nicotine-containing products 6 weeks before the first dose of study drug. Former smokers with greater than 10 pack years of smoking history are excluded.
Part 2 Major Inclusion Criteria:
- Confirmed diagnosis of CF
- Forced expiratory volume in 1 second ≥50% and ≤100% of predicted mean value for age, sex, and height
- a) Not eligible for CFTR modulators based on having mutations of CFTR gene on both alleles that are not responsive to CFTR modulator therapy OR
- b) Eligible for CFTR modulators (based on local prescribing information) but not using CFTR modulators due to intolerance or contraindications
Part 2 Major Exclusion Criteria:
- Hepatic cirrhosis with portal hypertension, moderate hepatic impairment (Child Pugh Score 7 to 9), or severe hepatic impairment (Child Pugh Score 10 to 15)
- An acute upper or lower respiratory infection, pulmonary exacerbation, or changes in therapy (including antibiotics) for sinopulmonary disease within 4 weeks before the first dose of study drug
- Lung infection with organisms associated with a more rapid decline in pulmonary status
- Arterial oxygen saturation on room air less than 94% at screening
- Treatment with a CFTR modulator (Kalydeco, Trikafta, Symdeko, Orkambi, or Alyftrek) within 12 weeks of Screening
Other protocol defined Inclusion/Exclusion criteria may apply.
Part 3 Major Inclusion Criteria:
- Confirmed diagnosis of CF
- Forced expiratory volume in 1 second ≥50% and ≤100% of predicted mean value for age, sex, and height
- a) Not eligible for CFTR modulators based on having mutations of CFTR gene on both alleles that are not responsive to CFTR modulator therapy OR
- b) Eligible for dual or triple CFTR modulators (based on local prescribing information) but not using CFTR modulators due to intolerance or contraindications
Part 3 Major Exclusion Criteria:
- Hepatic cirrhosis with portal hypertension, moderate hepatic impairment (Child Pugh Score 7 to 9), or severe hepatic impairment (Child Pugh Score 10 to 15)
- An acute upper or lower respiratory infection, pulmonary exacerbation, or changes in therapy (including antibiotics) for sinopulmonary disease within 4 weeks before the first dose of study drug
- Lung infection with organisms associated with a more rapid decline in pulmonary status
- Arterial oxygen saturation on room air less than 94% at screening
- Treatment with a CFTR modulator (Kalydeco, Trikafta, Symdeko, Orkambi, or Alyftrek) within 12 weeks of Screening
Other protocol defined Inclusion/Exclusion criteria may apply.
Trial locations and contacts
23 sites in 5 countries.
23 sites in 5 countries
United States13 sites
Emory University
Atlanta, Georgia, 30322
The University of Alabama at Birmingham
Birmingham, Alabama, 35294
Boston Children's Hospital
Boston, Massachusetts, 02215
The University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, 27599
UT Southwestern Medical Center
Dallas, Texas, 75390
National Jewish Health
Denver, Colorado, 80206
Stanford University
Palo Alto, California, 94304
University of Pittsburgh
Pittsburgh, Pennsylvania, 15213
Oregon Health & Science University
Portland, Oregon, 97239
UCSD
San Diego, California, 92037
University of Washington
Seattle, Washington, 98195
University of Arizona
Tucson, Arizona, 85719
New York Medical College
Valhalla, New York, 10595
United Kingdom6 sites
University Hospitals Birmingham
Birmingham
Royal Papworth Hospital
Cambridge
Leeds Teaching Hospitals
Leeds
King's College Hospital
London
Nottingham University Hospitals
Nottingham
University Hospital Southampton
Southampton
France2 sites
Centre Hospitalier Régional Universitaire de Montpellier - Hôpital Arnaud de Villeneuve
Montpellier
Hôpital Necker Enfants Malades
Paris
About this study
Official title: A Phase 1/2, Multicenter Study Evaluating the Safety, Tolerability, and Biodistribution of RCT2100 With Single-Ascending Doses in Healthy Participants and Multiple-Ascending Doses and Proof-of-Concept in Participants With Cystic Fibrosis
This is the first-in-human study with RCT2100 and is designed to provide safety and tolerability data for future clinical studies.
Read the detailed description
This is a multi-part study to assess the safety, tolerability, and biodistribution of a single ascending dose of inhaled RCT2100 administered via nebulizer to healthy participants (Part 1), the safety and tolerability of multiple-ascending doses of inhaled RCT2100 administered to participants with CF (Part 2), and the safety and tolerability of RCT2100 co-administered with ivacaftor in participants with CF (Part 3).
- Conditions
- Cystic Fibrosis
- Being tested
- RCT2100, Placebo, Ivacaftor
- Keywords
- Cystic Fibrosis, CF, mRNA
- Medical subject headings
- Cystic Fibrosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
RCT2100Drug
RCT2100 supplied as varying dose strengths administered via oral inhalation using nebulizer
PlaceboOther
Placebo of similar volumes to experimental dose strengths administered via oral inhalation using nebulizer
RCT2100Drug
RCT2100 supplied as varying dose strengths administered via oral inhalation using nebulizer for 4 weeks
RCT2100Drug
RCT2100 supplied at a single dose strength administered via oral inhalation using nebulizer for 12 weeks
IvacaftorDrug
ivacaftor administered orally for 6 weeks
RCT2100Drug
RCT2100 supplied at varying dose strengths. Co- administered via oral inhalation using nebulizer for 4 weeks with ivacaftor after initial 2 weeks of ivacaftor dosing run in period
| Study group | Role | What they receive |
|---|---|---|
| RCT2100 (Part 1) | Experimental | RCT2100 single dose Receives: Drug: RCT2100 |
| Placebo (Part 1) | Placebo comparator | Placebo single dose Receives: Other: Placebo |
| RCT2100 (Part 2) 4 week | Experimental | RCT2100 multiple dose Receives: Drug: RCT2100 |
| RCT2100 (Part 2) 12 week | Experimental | RCT2100 multiple dose Receives: Drug: RCT2100 |
| Experimental: RCT2100 (Part 3) 6 week | Experimental | RCT2100 multiple dose Receives: Drug: Ivacaftor; Drug: RCT2100 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Part 1: The number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs).
Safety and tolerability as assessed by number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)
Measured: From Baseline Through Day 29
Part 2: The number of participants with CF with AEs and SAEs.
Safety and tolerability of multiple-ascending doses of inhaled RCT2100 administered to participants with CF
Measured: From Day 1 through Safety Follow-up, Week 24
Part 3: The number of participants with CF with AEs and SAEs.
To assess the safety and tolerability of RCT2100 co-administered with ivacaftor in participants with CF.
Measured: From Day 1 through Safety Follow-up, Week 24
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Feb 2024
- Study start1 Feb 2024
- Primary completionNov 2026 (estimated)
- Study completionNov 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cystic FibrosisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 128 participants (actual)
Sponsor and investigators
- Lead sponsor
- ReCode Therapeutics
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- John Matthews, MBBS, MCRP, PhD, Study chair, ReCode Therapeutics, Inc.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06237335
- Sponsor's protocol ID
- RCT2100-101
- Other IDs
- 2024-512169-15
- Status last verified
- Aug 2026
- First submitted
- 23 Jan 2024
- Last updated
- 19 Aug 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 1/2, Multicenter Study Evaluating the Safety, Tolerability, and Biodistribution of RCT2100 With Single-Ascending Doses in Healthy Participants and Multiple-Ascending Doses and Proof-of-Concept in Participants With Cystic Fibrosis
- ClinicalTrials.gov ID
- NCT06237335
- Acronym / sponsor ID
- RCT2100-101
- Conditions
- Cystic Fibrosis
- Keywords
- Cystic Fibrosis, CF, mRNA
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 128 participants (actual)
- Lead sponsor
- ReCode TherapeuticsIndustry (pharma, biotech, devices)
- Study start
- 1 Feb 2024 (actual)
- Primary completion
- Nov 2026 (estimated)
- Study completion
- Nov 2026 (estimated)
- First posted
- 1 Feb 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is the first-in-human study with RCT2100 and is designed to provide safety and tolerability data for future clinical studies.
Detailed description
This is a multi-part study to assess the safety, tolerability, and biodistribution of a single ascending dose of inhaled RCT2100 administered via nebulizer to healthy participants (Part 1), the safety and tolerability of multiple-ascending doses of inhaled RCT2100 administered to participants with CF (Part 2), and the safety and tolerability of RCT2100 co-administered with ivacaftor in participants with CF (Part 3).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 5
| Arm | Type | Receives |
|---|---|---|
| RCT2100 (Part 1) | Experimental | Drug: RCT2100RCT2100 single dose |
| Placebo (Part 1) | Placebo comparator | Other: PlaceboPlacebo single dose |
| RCT2100 (Part 2) 4 week | Experimental | Drug: RCT2100RCT2100 multiple dose |
| RCT2100 (Part 2) 12 week | Experimental | Drug: RCT2100RCT2100 multiple dose |
| Experimental: RCT2100 (Part 3) 6 week | Experimental | Drug: Ivacaftor, Drug: RCT2100RCT2100 multiple dose |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| RCT2100RCT2100 supplied as varying dose strengths administered via oral inhalation using nebulizer | Drug | RCT2100 (Part 1) |
| PlaceboPlacebo of similar volumes to experimental dose strengths administered via oral inhalation using nebulizer | Other | Placebo (Part 1) |
| RCT2100RCT2100 supplied as varying dose strengths administered via oral inhalation using nebulizer for 4 weeks | Drug | RCT2100 (Part 2) 4 week |
| RCT2100RCT2100 supplied at a single dose strength administered via oral inhalation using nebulizer for 12 weeks | Drug | RCT2100 (Part 2) 12 week |
| Ivacaftorivacaftor administered orally for 6 weeks | Drug | Experimental: RCT2100 (Part 3) 6 week |
| RCT2100RCT2100 supplied at varying dose strengths. Co- administered via oral inhalation using nebulizer for 4 weeks with ivacaftor after initial 2 weeks of ivacaftor dosing run in period | Drug | Experimental: RCT2100 (Part 3) 6 week |
Primary outcome
Part 1: The number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs).
Time frame: From Baseline Through Day 29
Safety and tolerability as assessed by number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)
Part 2: The number of participants with CF with AEs and SAEs.
Time frame: From Day 1 through Safety Follow-up, Week 24
Safety and tolerability of multiple-ascending doses of inhaled RCT2100 administered to participants with CF
Part 3: The number of participants with CF with AEs and SAEs.
Time frame: From Day 1 through Safety Follow-up, Week 24
To assess the safety and tolerability of RCT2100 co-administered with ivacaftor in participants with CF.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Aug 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
John Matthews, MBBS, MCRP, PhD study chair
ReCode Therapeutics, Inc.
23 sites in 5 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing RCT2100 and Ivacaftor in people with Cystic Fibrosis, run by ReCode Therapeutics at 23 sites in 5 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 19 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 23 sites in United States, United Kingdom, France, Netherlands, New Zealand. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Part 1: The number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs). (time frame: From Baseline Through Day 29). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Aug 2026.