SAPROPTERIN DIHYDROCHLORIDE
Details
- Status
- Prescription
- First Approved
- 2019-05-10
- Routes
- ORAL
- Dosage Forms
- TABLET, POWDER
SAPROPTERIN DIHYDROCHLORIDE Approval History
What SAPROPTERIN DIHYDROCHLORIDE Treats
2 indicationsSAPROPTERIN DIHYDROCHLORIDE is approved for 2 conditions since its original approval in 2019. These indications span multiple therapeutic areas including oncology, immunology, and more.
- Hyperphenylalaninemia
- Phenylketonuria
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Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
SAPROPTERIN DIHYDROCHLORIDE FDA Label Details
ProIndications & Usage
Sapropterin dihydrochloride tablets are indicated to reduce blood phenylalanine (Phe) levels in adult and pediatric patients one month of age and older with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (BH4-) responsive Phenylketonuria (PKU). Sapropterin dihydrochloride tablets are to be used in conjunction with a Phe-restricted diet. Sapropterin dihydrochloride tablets are a phenylalanine hydroxylase activator indicated to reduce blood phenylalanine (Phe) levels in adult and pediatric patients one month of age and older with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin- (...
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.