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EBGLYSS (LEBRIKIZUMAB-LBKZ)

ELI LILLY AND CO · FDA-approved approved Quality 6/100

EBGLYSS (generic name: LEBRIKIZUMAB-LBKZ) is a Interleukin-13 Antagonist [EPC] drug developed by ELI LILLY AND CO. It is currently FDA-approved.

At a glance

Generic nameLEBRIKIZUMAB-LBKZ
SponsorELI LILLY AND CO
Drug classInterleukin-13 Antagonist [EPC]
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

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Frequently asked questions about EBGLYSS

What is EBGLYSS?

EBGLYSS (LEBRIKIZUMAB-LBKZ) is a Interleukin-13 Antagonist [EPC] drug developed by ELI LILLY AND CO.

Who makes EBGLYSS?

EBGLYSS is developed and marketed by ELI LILLY AND CO (see full ELI LILLY AND CO pipeline at /company/eli-lilly).

What is the generic name of EBGLYSS?

LEBRIKIZUMAB-LBKZ is the generic (nonproprietary) name of EBGLYSS.

What drug class is EBGLYSS in?

EBGLYSS belongs to the Interleukin-13 Antagonist [EPC] class. See all Interleukin-13 Antagonist [EPC] drugs at /class/interleukin-13-antagonist-epc.

What development phase is EBGLYSS in?

EBGLYSS is FDA-approved (marketed).

What are the side effects of EBGLYSS?

Common side effects of EBGLYSS include Conjunctivitis, Injection site reactions, Herpes zoster. Serious adverse events: Eosinophilia (>5000 cells/mcL), Keratitis.

Related

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