
Clinical Studies
Herozyme has been developed as a biosimilar to the reference medicine Aldurazyme®, meaning it is designed to have similar effectiveness, safety, and biological activity. The effectiveness and safety of Herozyme were evaluated in a Phase III clinical study.
Clinical Studies
Herozyme has been developed as a biosimilar to the reference medicine Aldurazyme®, meaning it is designed to have similar effectiveness, safety, and biological activity. The effectiveness and safety of Herozyme were evaluated in a Phase III clinical study.
The study was conducted in pediatric patients with MPS I. The design of the study allowed doctors to observe whether Herozyme could maintain the benefits already achieved with the reference medicine.
Clinical data show that Herozyme provides similar effectiveness, biological activity, and safety to the reference laronidase, supporting its use in the long-term management of mucopolysaccharidosis type I.
Effectiveness Results
Safety Results
- A total of 30 adverse events were reported during the study
- Most events were mild to moderate (Grade 1–2)
- The most common event was nasopharyngitis
- Mild infusion-related reactions occurred in both treatment periods
- Serious adverse events were related to underlying disease, not the study drugs
Overall:
- Adverse events were reported in 58.3% of patients during reference treatment
- And 50% during Herozyme treatment
No new or unexpected safety concerns were identified, and the overall safety profile of Herozyme was comparable to the reference medicine.
Dosing and Administration
Dose:0.58mgperkgofbodyweight
Route:Intravenousinfusion
Frequency:Onceweekly
Infusiontime:Approximately3–4hours
The dosing schedule for Herozyme is identical to the reference product, supporting clinical interchangeability.
What These Results Mean
- Herozyme maintained disease control after patients switched from the reference medicine
- Key biochemical and clinical measures remained stable
- Effectiveness and safety were comparable to Aldurazyme®
- The study supports Herozyme as a reliable alternative for ongoing treatment of MPS I



