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Exkivity (mobocertinib)

Region
🇪🇺 EU
Active substance
mobocertinib
Company
Takeda Pharma A/S
Status
Application withdrawn
Therapeutic area
Carcinoma, Non-Small-Cell Lung
Application
EMEA/H/C/005621
ATC
L01EB
Official record
www.ema.europa.eu

Indication

Treatment of adult patients with epidermal growth factor receptor (EGFR) exon 20 insertion mutation-positive locally advanced or metastatic non-small cell lung cancer (NSCLC).

Regulatory milestones

No milestones recorded in the last year.

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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.