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NCX 470 NDA submitted in China by Ocumension

August 10, 2026

What is the news ?

Ocumension has submitted an NDA to China’s National Medical Products Administration (NMPA) for NCX 470 to lower intraocular pressure in patients with open-angle glaucoma or ocular hypertension, using the same data package as recently submitted to the U.S. FDA.

What does it mean ?

NDAs for NCX 470 have now been submitted in two major territories, the United States and China, putting NCX 470 on the way to multiple approvals and launches over the next 12 to 24 months.

What are the next steps ?

Multiple NCX 470 clinical, approval and launch milestone events are expected over the next 12 to 18 months, including regulatory review in China and ongoing Phase 3 trials in Japan.
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