Wednesday, July 8, 2026

Drug profile · INN

pegulicianine acetate

pegulicianine acetate (LUMISIGHT) is a diagnostic agent. Route of administration: intravenous. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 3
News articles 0
Drug details — pegulicianine acetate
US status
approved
Class
Route
INTRAVENOUS
Patents
0
Programs
3
Data quality
0.84

Quick answer

pegulicianine acetate (LUMISIGHT) is a diagnostic agent. Route of administration: intravenous. Current US regulatory status: approved.

Key facts

INN pegulicianine acetate
Brand LUMISIGHT
Mechanism Diagnostic agent
Route INTRAVENOUS
Formulation POWDER

Mechanism of action

Diagnostic agent

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. Peg interferon alpha-2b Phase 3 · Universal Integrated · Hepatitis C
  2. Guli capsule Approved · Chinese Academy of · Knee Osteoarthritis
  3. Polyethylene glycol (PEG) Unknown · Hospital Authority · Acute Kidney Injury

Frequently asked questions

What is pegulicianine acetate?

pegulicianine acetate (LUMISIGHT) is a diagnostic agent. Route of administration: intravenous. Current US regulatory status: approved.

What is the brand name for pegulicianine acetate?

LUMISIGHT is a marketed brand name for pegulicianine acetate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of pegulicianine acetate?

pegulicianine acetate 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.