March 13, 2019
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FDA approves Rocklatan for open-angle glaucoma, ocular hypertension

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The FDA has approved Rocklatan, a once-daily IOP-lowering eye drop, for patients with open-angle glaucoma or ocular hypertension, Aerie Pharmaceuticals announced in a press release.

A fixed-dose combination of netarsudil and latanoprost, Rocklatan — previously known as Roclatan — is designed to target the trabecular meshwork, which is considered the main cause of elevated IOP, the release said.

FDA approval is based on data from two phase 3 trials in which Rocklatan demonstrated statistically significant IOP reduction compared with its two individual components.

Aerie plans to launch Rocklatan in the United States in the second quarter.