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Clinical Trial Summary

This is a Phase 1/2, open-label, dose escalation study to evaluate the safety, efficacy and tolerability of BMN 307 in adult PKU subjects with PAH deficiency. Participants will receive a single administration of BMN 307 and will be followed for safety and efficacy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04480567
Study type Interventional
Source BioMarin Pharmaceutical
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date September 24, 2020
Completion date December 2027

See also
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