COMPANY
Eisai Inc.
FDA-approved therapeutic company FDA-cleared device company
Timeline
- FDA FDA New indication / efficacy supplement: LENVIMA (lenvatinib mesylate) — NDA206947/35, Sep 24, 2026. Applicant at approval: Eisai Inc. source ↗
- Partnership Partnership / licensing announced Sep 14, 2026. Source: company's own press page. source ↗
- FDA FDA New indication / efficacy supplement: LEQEMBI IQLIK (lecanemab-irmb) — BLA761375/1, Jul 13, 2026. Applicant at approval: Eisai Inc. source ↗
- Raise Private placement: amount not published, announced Jun 15, 2026. Source: company's own press page. source ↗
- FDA FDA New indication / efficacy supplement: LENVIMA (lenvatinib mesylate) — NDA206947/33, Jan 29, 2025. Applicant at approval: Eisai Inc. source ↗
- FDA FDA New indication / efficacy supplement: LEQEMBI (lecanemab-irmb) — BLA761269/5, Jan 24, 2025. Applicant at approval: Eisai Inc. source ↗
Funding
FDA records (last 2 years)
- FDA New indication / efficacy supplement: LENVIMA (lenvatinib mesylate) — NDA206947/35, Sep 24, 2026. Applicant at approval: Eisai Inc. source ↗
- FDA New indication / efficacy supplement: LEQEMBI IQLIK (lecanemab-irmb) — BLA761375/1, Jul 13, 2026. Applicant at approval: Eisai Inc. source ↗
- FDA New indication / efficacy supplement: LENVIMA (lenvatinib mesylate) — NDA206947/33, Jan 29, 2025. Applicant at approval: Eisai Inc. source ↗
- FDA New indication / efficacy supplement: LEQEMBI (lecanemab-irmb) — BLA761269/5, Jan 24, 2025. Applicant at approval: Eisai Inc. source ↗
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