CompletedPHASE1, PHASE2NCT01142154
Pharmacokinetics and Safety Study of Single and Multiple Oral Doses Prodarsan™ in Patients With Cockayne Syndrome
Studying Cockayne syndrome
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
- DNage B.V.
- Principal Investigator
- Edward Neilan, MDBoston Children's Hospital
- Intervention
- Prodarsan(drug)
- Enrollment
- 5 enrolled
- Eligibility
- 2-10 years · All sexes
- Timeline
- 2010 – 2011
Study locations (1)
- Children's Hospital Boston, Boston, Massachusetts, United States
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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