CompletedPhase 1NCT04085666
Pharmacodynamics, Safety, Tolerability and Pharmacokinetics of CDX-6114 in Patients With Phenylketonuria (PKU)
Studying Classic phenylketonuria
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
- Société des Produits Nestlé (SPN)
- Principal Investigator
- Damon BellLinear Clinical Research
- Intervention
- CDX 6114(drug)
- Enrollment
- 18 enrolled
- Eligibility
- 18-55 years · All sexes
- Timeline
- 2019 – 2020
Study locations (2)
- Linear Clinical Research Ltd, Nedlands, Western Australia, Australia
- Profil Institut für Stoffwechselforschung GmbH, Neuss, Germany
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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