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Pegaptanib

SENSORY ORGANS

Also known as: EYE001, macugen, NX1838, pegaptanib octasodium, pegaptanib sodium

FDA approvedATC S01LA03

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Pegaptanib is a drug catalogued in DrugCentral. It was first approved by the FDA in 2004. DrugCentral lists 1 molecular target, including VEGFA. Recorded indications include Exudative age-related macular degeneration.

  • Molecular targets: VEGFA (1 listed in DrugCentral).
  • Indications: Exudative age-related macular degeneration.
  • ATC code: S01LA03 (Antineovascularisation agents).

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (1)

  • Exudative age-related macular degeneration

Mechanism & targets

Molecular targets (1)

TargetGeneActionActivity
Vascular endothelial growth factor AVEGFAantagonist—

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
2004-12-17FDA—VALEANT PHARMS LLC

ATC classification

ATC codeTherapeutic hierarchy
S01LA03SENSORY ORGANS › OPHTHALMOLOGICALS › OCULAR VASCULAR DISORDER AGENTS › Antineovascularisation agents

Chemical structure

Molecular formula—
Molecular weight—
CAS number—
InChIKey—
PubChem CID—

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Pegaptanib used for?

DrugCentral lists the following indications for Pegaptanib: Exudative age-related macular degeneration.

How does Pegaptanib work?

Its molecular targets in DrugCentral include VEGFA (antagonist).

When was Pegaptanib first approved?

Pegaptanib was first approved by the FDA in 2004.

Browse: all drugs starting with P · drug guides by category · protein targets A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

Status—
First approval2004-12-17
AgencyFDA
Targets1
Indications1
Formula—
DrugCentral ID4905
Interactive profile