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Study details
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A Phase 2 Trial Evaluating Safety and Tolerability of RCT2100

ReCode Therapeutics
NCT IDNCT06237335ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

192

Study length

about 2.9 years

Ages

18–60

Locations

13 sites in AL, AZ, CA +9

About this study

Researchers are testing the safety and tolerability of a new treatment, RCT2100, in healthy people and people with cystic fibrosis. The trial will involve different doses of RCT2100 administered through inhalation, either alone or with ivacaftor.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Placebo
  • 2.Take Ivacaftor
  • 3.Take RCT2100
PhasePhase 2
DrugIvacaftor
Routeoral
Primary goalPart 1: The number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low12%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

ivacaftor

Drug routes

oral (Oral Tablet)

Endpoints

Primary: Part 1: The number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)., Part 2: The number of participants with CF with AEs and SAEs., Part 3: The number of participants with CF with AEs and SAEs.

Body systems

Respiratory