Drug profile · INN
plozasiran
REDEMPLO
plozasiran (REDEMPLO) is an FDA-listed pharmaceutical active ingredient. Associated with Arrowhead Pharmaceuticals Ireland Limited.
Drug details — plozasiran
- Class
- Cardiovascular system (C10)
- Route
- —
- Patents
- 20
- Programs
- 9
- Data quality
- 0.89
Quick answer
plozasiran (REDEMPLO) is an FDA-listed pharmaceutical active ingredient. Associated with Arrowhead Pharmaceuticals Ireland Limited.
Key facts
Approval history
| Authority | Status | Date |
|---|---|---|
| EMA | unknown | — |
Recent coverage
Plozasiran TGA Approval: REDEMPLO® Now Available in Australia for FCS
Arrowhead Pharmaceuticals has secured TGA approval for REDEMPLO® (plozasiran) in Australia, marking a significant step in providing treatment options for patients with Familial Chylomicronemia Syndrome (FCS). This approval expands global access to the novel therapy for this rare genetic disorder.
Plozasiran TGA Approval in Australia for FCS Patients
Arrowhead Pharmaceuticals has announced the Therapeutic Goods Administration (TGA) approval of REDEMPLO® (plozasiran) in Australia for patients with Familial Chylomicronemia Syndrome (FCS). This landmark decision broadens global access to a crucial treatment for this rare genetic disorder.
Pipeline programs
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Frequently asked questions
What is plozasiran?
plozasiran (REDEMPLO) is an FDA-listed pharmaceutical active ingredient. Associated with Arrowhead Pharmaceuticals Ireland Limited.
What is the brand name for plozasiran?
REDEMPLO is a marketed brand name for plozasiran. Check FDA Drugs@FDA for the current US label holder and prescribing information.