Danyelza is given by a doctor or nurse and billed by the clinic, not a pharmacy. Your care team and your insurance decide which product you get, so ask them what you’d pay.

How do you pay?

How to pay the least

Given by your care team

Billed by the clinic

Danyelza is given by a doctor or nurse, not picked up at a pharmacy.

  1. Ask your care team or your plan what you’d pay before your visit.

Compare every option

Question
Brand nameDanyelza
Authorized genericnaxitamab
Regular genericnaxitamab
What you’d pay
Cash priceAsk the pharmacy
Not soldThere isn’t one
Not soldAsk the pharmacy
Same as Danyelza?
The original
–
–

Brand nameThe maker’s card

Y-mAbs Connect Co-pay Program

Savings card from Y-mAbs Therapeutics

No insuranceNeeds insuranceNo cash price listed.
Insurance · as little as $0 an infusion

Sign up on ymabsconnect.com 

In the maker’s words

“This program could help lower out-of pocket costs of DANYELZA to $0 for eligible patients.”

From the maker’s offer on ymabsconnect.com, checked November 2, 2026. Co-pay cards can’t be used with Medicare (including Medicare Advantage), Medicaid, TRICARE or VA.

Authorized genericNot sold

There isn’t one. An authorized generic is Danyelza itself, from the same company, sold without the brand name, and usually for less. For now Danyelza is the only choice; its maker’s savings card can lower what you pay.

See the brand name →

Regular genericNot sold

Danyelza is a biologic. Biologics don’t have generics, but some have biosimilars or an unbranded version from the same maker. Ask your pharmacist or prescriber whether one is sold. Generics usually come once the brand’s patents and exclusivity end. Until then, the maker’s savings card is the way to pay less.

See the brand name →

What it’s used for

What the FDA label says

DANYELZA is a GD2-binding monoclonal antibody indicated, in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF), for the treatment of pediatric patients 1 year of age and older and adult patients with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow who have demonstrated a partial response, minor response, or stable disease to prior therapy.

This indication is approved under accelerated approval based on overall response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).

Source: the FDA label for Danyelza (BTG International Inc.), August 7, 2026. Full label on DailyMed 

Good to know