CompletedPhase 1NCT05737485
Study Evaluating the Safety and Tolerability of RCT1100 in Healthy and PCD Subjects
Studying Primary ciliary dyskinesia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- ReCode Therapeutics
- Principal Investigator
- John Matthews, MBBS, MCRP, PhDReCode Therapeutics, Inc.
- Intervention
- RCT1100(drug)
- Enrollment
- 9 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2023 – 2025
Study locations (4)
- PPD - Las Vegas Research Unit, Las Vegas, Nevada, United States
- Macquarie University, Sydney, New South Wales, Australia
- New Zealand Clinical Research, Auckland, New Zealand
- Royal Brompton Hospital, London, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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