Wednesday, July 8, 2026

Drug profile · INN

plozasiran sodium

plozasiran sodium (REDEMPLO) is an FDA-listed pharmaceutical active ingredient. Associated with Arrowhead Pharmaceuticals Ireland Limited. Route of administration: subcutaneous. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 20
Pipeline programs 3
News articles 0
Drug details — plozasiran sodium
US status
approved
Class
Route
SUBCUTANEOUS
Patents
20
Programs
3
Data quality
0.89

Quick answer

plozasiran sodium (REDEMPLO) is an FDA-listed pharmaceutical active ingredient. Associated with Arrowhead Pharmaceuticals Ireland Limited. Route of administration: subcutaneous. Current US regulatory status: approved.

Key facts

INN plozasiran sodium
Brand REDEMPLO
Route SUBCUTANEOUS
Formulation SOLUTION

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. Plozasiran Phase 3 · Arrowhead Pharmaceuticals Ireland · Familial Chylomicronemia
  2. Plozasiran Phase 3 · Arrowhead Pharmaceuticals Ireland · Familial Chylomicronemia Syndrome
  3. Plozasiran Phase 3 · Arrowhead Pharmaceuticals Ireland · Severe Hypertriglyceridemia
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Frequently asked questions

What is plozasiran sodium?

plozasiran sodium (REDEMPLO) is an FDA-listed pharmaceutical active ingredient. Associated with Arrowhead Pharmaceuticals Ireland Limited. Route of administration: subcutaneous. Current US regulatory status: approved.

What is the brand name for plozasiran sodium?

REDEMPLO is a marketed brand name for plozasiran sodium. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of plozasiran sodium?

plozasiran sodium has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.