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NCE-1 Intelligence & Market Opportunity

Ojemda

Tovorafenib
Anticancer
Oral Suspension

Ojemda is the first FDA-approved targeted therapy for children 6 months and older with relapsed or treatment-resistant pediatric low-grade glioma (pLGG) caused by certain BRAF gene changes.

Approval Date
23-Apr-24
NCE-1 Date
23-Apr-28
NCE Date
23-Apr-29
Commercial snapshot

Market performance & projections

Revenue ($M)
155
CAGR (%)
-20.47%
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
9
2027
25
2028
42
2029
62
2030
82
2031
103
2032
123
Molecule profile

Details & specifications

Molecule
Tovorafenib
Innovator
DAY ONE BIOPHARMACEUTICALS INC
Dosage Form
Oral Suspension
Strength
25 mg/mL
Therapeutic Category
Anticancer
Usage
To treat relapsed or refractory pediatric low-grade glioma
Good to know

Frequently asked questions

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