Zynlonta 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

Zynlonta 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 nameZynlonta
Authorized genericloncastuximab tesirine
Regular genericloncastuximab tesirine
What you’d pay
Cash priceAsk the pharmacy
Not soldThere isn’t one
Not soldAsk the pharmacy
Same as Zynlonta?
The original
–
–

Brand nameThe maker’s card

ADVANCING Patient Support copay program

Savings card from ADC Therapeutics America

No insuranceNeeds insuranceNo cash price listed.
Insurance · as little as $0 a dose

The card takes up to $25,000 a year off your co-pay.

Sign up on zynlonta.com 

Or call 1-855-690-0340.

In the maker’s words

“If you are commercially insured and eligible, ADVANCING Patient Support can help your doctor’s office enroll you in the copay program, in which you could pay as little as $0 per dose.”

From the maker’s offer on zynlonta.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 Zynlonta itself, from the same company, sold without the brand name, and usually for less. For now Zynlonta is the only choice; its maker’s savings card can lower what you pay.

See the brand name →

Regular genericNot sold

Zynlonta 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

ZYNLONTA is a CD19-directed antibody and alkylating agent conjugate indicated for the treatment of adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy, including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, DLBCL arising from low-grade lymphoma, and high-grade B-cell lymphoma.

This indication is approved under accelerated approval based on overall response rate. 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 Zynlonta (ADC Therapeutics America, Inc.), June 12, 2026. Full label on DailyMed 

Good to know