How do you pay?

How to pay the least

Ask for the cash price

Ojemda

We didn’t find one.

  1. Ask your pharmacy for Ojemda’s cash price, and one or two other pharmacies too.
  2. Ojemda’s savings card works only with insurance from a job or one you bought.

Compare every option

Question
Brand nameOjemda
Authorized generictovorafenib
Regular generictovorafenib
What you’d pay
Cash priceAsk the pharmacy
Not soldThere isn’t one
Not soldNone found
Same as Ojemda?
The original
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–

Brand nameThe maker’s card

OJEMDA Copay Program (EveryDay Support From Day One)

Savings card from Day One Biopharmaceuticals

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

Sign up on ojemda.com 

Or call 1-855-329-1246. See the offer on ojemda.com

In the maker’s words

“the OJEMDA Copay Program, which can lower out-of-pocket costs to as little as $0 per month…”

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

Maker’s card or discount card?

A discount card like GoodRx lowers the pharmacy’s cash price, but for a brand-name drug that price often stays high. Compare it with the maker’s card above. You can usually use one or the other on a fill, not both.

Authorized genericNot sold

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

See the brand name →

Regular genericNot sold

We didn’t find one. 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

OJEMDA is a kinase inhibitor indicated for the treatment of patients 6 months of age and older with relapsed or refractory pediatric low-grade glioma (LGG) harboring a BRAF fusion or rearrangement, or BRAF V600 mutation.

This indication is approved under accelerated approval based on 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 Ojemda (Day One Biopharmaceuticals, Inc.), September 2, 2025. Full label on DailyMed 

Good to know