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AHZANTIVE (AFLIBERCEPT-MRBB)

FORMYCON AG · FDA-approved approved ✓ Verified May 2026 Quality 9/100

AHZANTIVE (generic name: AFLIBERCEPT-MRBB) is a drug developed by FORMYCON AG. It is currently FDA-approved.

Aflibercept is a protein-based inhibitor of vascular endothelial growth factor A, long form. It belongs to the drug class of inhibitors and works by modulating the activity of vascular endothelial growth factor A.

At a glance

Generic nameAFLIBERCEPT-MRBB
SponsorFORMYCON AG
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about AHZANTIVE

What is AHZANTIVE?

AHZANTIVE (AFLIBERCEPT-MRBB) is a pharmaceutical drug developed by FORMYCON AG.

Who makes AHZANTIVE?

AHZANTIVE is developed and marketed by FORMYCON AG (see full FORMYCON AG pipeline at /company/formycon-ag).

What is the generic name of AHZANTIVE?

AFLIBERCEPT-MRBB is the generic (nonproprietary) name of AHZANTIVE.

What development phase is AHZANTIVE in?

AHZANTIVE is FDA-approved (marketed).

What are the side effects of AHZANTIVE?

Common side effects of AHZANTIVE include Conjunctival hemorrhage, Eye pain, Cataract, Vitreous detachment, Vitreous floaters, Intraocular pressure increased. Serious adverse events: Endophthalmitis, Retinal detachment, Retinal tear, Hypersensitivity.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing