Saturday, July 11, 2026

Drug profile · INN

naxitamab-gqgk

naxitamab-gqgk (DANYELZA) is a disialoganglioside gd2 binding agent. Route of administration: intravenous. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — naxitamab-gqgk
US status
approved
Class
Route
INTRAVENOUS
Patents
0
Programs
0
Data quality
0.84

Quick answer

naxitamab-gqgk (DANYELZA) is a disialoganglioside gd2 binding agent. Route of administration: intravenous. Current US regulatory status: approved.

Key facts

INN naxitamab-gqgk
Brand DANYELZA
Mechanism Disialoganglioside GD2 binding agent
Target Disialoganglioside GD2
Route INTRAVENOUS
Formulation SOLUTION

Mechanism of action

Disialoganglioside GD2 binding agent

Primary target: Disialoganglioside GD2

Approval history

Authority Status Date
FDA approved

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Frequently asked questions

What is naxitamab-gqgk?

naxitamab-gqgk (DANYELZA) is a disialoganglioside gd2 binding agent. Route of administration: intravenous. Current US regulatory status: approved.

What is the brand name for naxitamab-gqgk?

DANYELZA is a marketed brand name for naxitamab-gqgk. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of naxitamab-gqgk?

naxitamab-gqgk 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.