Friday, July 10, 2026

Drug profile · INN

sibeprenlimab-szsi

sibeprenlimab-szsi (VOYXACT) is an FDA-listed pharmaceutical active ingredient. Route of administration: injection. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 3
News articles 1
Drug details — sibeprenlimab-szsi

Quick answer

sibeprenlimab-szsi (VOYXACT) is an FDA-listed pharmaceutical active ingredient. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN sibeprenlimab-szsi
Brand VOYXACT
Route INJECTION
Formulation INJECTABLE

Approval history

Authority Status Date
FDA approved

Recent coverage

Pipeline programs

  1. Sibeprenlimab 400 mg Phase 3 · Otsuka Beijing Research · Immunoglobulin A Nephropathy
  2. Sibeprenlimab 400 mg s.c. Q4weeks Phase 3 · Otsuka Beijing Research · Immunoglobulin A Nephropathy
  3. Sibeprenlimab, Sibeprenlimab placebo Phase 2 · Otsuka Beijing Research · Treatment of Sjögren’s disease

Frequently asked questions

What is sibeprenlimab-szsi?

sibeprenlimab-szsi (VOYXACT) is an FDA-listed pharmaceutical active ingredient. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for sibeprenlimab-szsi?

VOYXACT is a marketed brand name for sibeprenlimab-szsi. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of sibeprenlimab-szsi?

sibeprenlimab-szsi 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.