Larotrectinib
- Part D specialty tier in 80% of formularies (2026Q3)
- VITRAKVI
Therapy management checklist
Screening, baseline and ongoing monitoring with the label's stated frequency, hold and discontinue criteria, and counseling points, each quoted from the FDA label.
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Storage and cold chain
Larotrectinib: storage and handling
- Refrigerate
- Yes, as the label states
Label statement
Store VITRAKVI oral solution in a refrigerator between 36° F to 46° F (2° C to 8° C).
- Freezing
- Do not freeze
Label statement
Do not freeze.
- Room temperature
- at or below 30°C (86°F)
Label statement
Store capsules at room temperature 20°C to 25°C (68°F to 77°F); temperature excursions between 15°C and 30°C (59°F to 86°F) are permitted [see USP Controlled Room Temperature].
- Back into the refrigerator
- Not addressed
- Light
- Not addressed
- Shaking
- Not addressed
All storage statements on the label (5)
- Store capsules at room temperature 20°C to 25°C (68°F to 77°F); temperature excursions between 15°C and 30°C (59°F to 86°F) are permitted [see USP Controlled Room Temperature].
- Do not freeze.
- Store VITRAKVI oral solution in a refrigerator between 36° F to 46° F (2° C to 8° C).
- Store VITRAKVI capsules at room temperature between 68˚F to 77˚F (20˚C to 25˚C).
- Store VITRAKVI oral solution in the refrigerator between 36° F to 46° F (2° C to 8° C).
FDA label version 21, effective May 22, 2026. DailyMed
Dosing and titration calendar
Built only from the schedules the label states (loading, titration, day schedules, cycles and weight bands). Steps the label states in words the calendar cannot place are shown, not guessed.
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Medicare Part D coverage
5,496 Part D plans, CMS formulary files 2026Q3. Look up tier, PA, step therapy and quantity limits by plan
Patient assistance
No manufacturer program page is listed for this drug yet.
Independent foundations and the full directory (checked 2026-11-06). Eligibility and amounts are set by each program; open its page for them.
For licensed clinicians. Use with clinical judgment. Statements are quoted from the FDA label; confirm against the label for the product you are using.