TerminatedPhase 1NCT02907294
Study to Assess the Safety, Tolerability and Pharmacokinetic Profile of PBF-999 "After Multiple Oral Doses" in Healthy Volunteers
Studying Huntington disease
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
- Palobiofarma SL
- Principal Investigator
- Joan Martinez, MDCIM-Sant Pau
- Intervention
- PBF-999 / 160 mg(drug)
- Enrollment
- 8 enrolled
- Eligibility
- 18-45 years · All sexes
- Timeline
- 2016 – 2016
Study locations (1)
- CIM-Sant Pau, Barcelona, Barcelona, Spain
Collaborators
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
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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