Takeda's Growth Plan Bears Fruit with FDA Nod for Niche Lung Cancer Drug Exkivity
Takeda's oral med, Exkivity, has secured a conditional FDA nod for previously treated non-small cell lung cancer with EGFR exon 20 insertion mutations, marking the company's first win after several setbacks in its Wave 1 pipeline. The approval comes as a significant milestone for Takeda, which aims to rival Johnson & Johnson's Rybrevant, a bispecific antibody for the same niche patient group.
Key Takeaways:
- Takeda's Exkivity has been granted a conditional FDA approval for non-small cell lung cancer with EGFR exon 20 insertion mutations.
- Exkivity will compete with Johnson & Johnson's Rybrevant in the niche patient group.
- The approval marks Takeda's first win after several setbacks in its Wave 1 pipeline.
- Takeda's growth plan has borne fruit with the FDA nod, positioning the company for success in the competitive lung cancer market.
- Exkivity's approval comes with certain conditions, which the company must meet to gain full approval.
- Takeda must provide additional data to support the approval of Exkivity.
Statistics:
- 95: Number of vials with floating material reported through September 5, according to Pfizer.
- $108 million: Amount raised by IASO Biotherapeutics in series C funding for cell therapies, antibodies, and autoimmune disease treatment.
- $140 million: Amount Haisco will pay to license Biosplice's phase 3 osteoarthritis drug in China.
- 50-50: Collaboration ratio between Everest Medicines and Providence Therapeutics for mRNA platform programs.
Sources:
- FiercePharma: "Rivaling J&J, Takeda's growth plan bears fruit with FDA nod for niche lung cancer drug Exkivity"
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