osudhkosh

Generic

Faricimab

1 brands available in the market

At a glance

Faricimab is a bispecific antibody used for the treatment of neovascular age-related macular degeneration, diabetic macular edema, and macular edema secondary to retinal vein occlusion.

Description

Faricimab is a humanized bispecific immunoglobulin G1 (IgG1) antibody that acts through inhibition of two distinct pathways by neutralization of both Ang-2 and vascular endothelial growth factor A (VEGF-A). Ang-2 causes vascular instability and sensitizes blood vessels to the activity of VEGF-A. Ang-2 and VEGF-A synergistically increase vascular permeability and stimulate neovascularization.

By dual inhibition of Ang-2 and VEGF-A, faricimab reduces vascular permeability and inflammation, inhibits pathological angiogenesis and restores vascular stability.

Indications
  • Neovascular (Wet) AMD: Used for treatment of age-related macular degeneration.
  • Diabetic Macular Edema (DME): Used for treatment of DME.
  • Macular Edema Secondary to RVO: Used for treatment of macular edema due to retinal vein occlusion.
Therapeutic class

Ophthalmic (Anti-VEGF)

Pharmacological class

Bispecific Angiopoietin-2 and VEGF Inhibitor

Pharmacology

Faricimab is a humanized bispecific immunoglobulin G1 (IgG1) antibody that acts through inhibition of two distinct pathways by neutralization of both Ang-2 and VEGF-A. Ang-2 causes vascular instability and sensitizes blood vessels to the activity of VEGF-A. Ang-2 and VEGF-A synergistically increase vascular permeability and stimulate neovascularization.

Mechanism of action

Faricimab reduces vascular permeability and inflammation, inhibits pathological angiogenesis and restores vascular stability through dual inhibition of Ang-2 and VEGF-A.

Dosage

Adult Dose (Intravitreal):

  • Neovascular AMD: First 4 doses: 6 mg (0.05 mL) every 4 weeks, then 6 mg up to every 16 weeks.
  • Diabetic Macular Edema (DME): First 4 doses: 6 mg every 4 weeks, then 6 mg up to every 16 weeks.
  • Macular Edema Secondary to RVO: 6 mg every 4 weeks.
Administration

For intravitreal injection only. Must be administered by a qualified physician experienced in intravitreal injections. Each vial should only be used for the treatment of a single eye.

Missed dose

If you miss a dose, please consult your ophthalmologist.

Side effects

Side Effects:

  • Intravitreal injection-related reactions
  • Intraocular inflammation
  • Infections
  • Increased blood pressure
Precautions & warnings

Precautions:

  • Contraindicated in patients with ocular or periocular infections.
  • Contraindicated in patients with active intraocular inflammation.
  • Contraindicated in patients with known hypersensitivity.
  • Monitoring between dosing visits should be scheduled based on patient status and physician's discretion.
Contraindications

Contraindications:

  • Ocular or periocular infections
  • Active intraocular inflammation
  • Hypersensitivity to faricimab or any excipients
Drug interactions

Drug Interactions: No known interactions.

Food interactions

Food Interactions: No interactions with food.

Use in pregnancy

Use in Pregnancy: No data from use in pregnant women; caution required.

Pregnancy Category: C — always consult a doctor before taking during pregnancy.

Use in lactation

Use in Lactation: It is not known whether Faricimab is excreted in human milk; caution required.

Pediatric use

Pediatric Use: Safety and efficacy not established.

Geriatric use

Geriatric Use: In clinical studies, approximately 58% of patients were >=65 years; no significant differences in efficacy or safety with increasing age.

Renal / hepatic impairment

Renal Impairment: No dose adjustment required.

Hepatic Impairment: Safety and efficacy not studied.

Overdose effects

Overdose: Limited information on overdose; symptomatic treatment.

Storage conditions

Storage: Store at 2-8 degree C. Do not freeze. Keep in original carton to protect from light.

Chemical structure

Faricimab

Common questions

Q1: What is Faricimab used for?
It is used for neovascular AMD, diabetic macular edema, and macular edema secondary to RVO.
Q2: How is it administered?
It is administered as intravitreal injection by an ophthalmologist.
Q3: What is the dosage?
First 4 doses: 6 mg every 4 weeks, then up to every 16 weeks.
Q4: Who should not use it?
Patients with ocular infections, active intraocular inflammation, or hypersensitivity.
⚠️ This information is for educational purposes only — not a substitute for medical advice. Consult a registered physician before taking any medicine.