Response to Kuvan® in Subjects With Phenylketonuria (PKU) in a 4 Weeks Testing Period

Update Il y a 4 ans
Reference: NCT01082328

Woman and Man

  • | Country :
  • Norway
  • | organs :
  • -
  • | Specialty :
  • -

Extract

The primary objective of the study is to evaluate the proportion of responders (that is, greater than or equal to [>=] 30 percent reduction from Baseline in blood phenylalanine [Phe] level) to treatment with Kuvan® (sapropterin dihydrochloride) 20 milligram per kilogram per day (mg/kg/day) for 28 days.


Inclusion criteria

  • Phenylketonuria

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