OKYO Pharma (OKYO) announces that the U.S. Food and Drug Administration, FDA, has granted Fast Track designation, FTD, to urcosimod for the treatment of neuropathic corneal pain, NCP. Gary Jacob, Ph.D., Chief Executive Officer of OKYO Pharma, expressed his enthusiasm about the FDA’s decision: “We are thrilled with the FDA’s Fast Track designation for urcosimod in the treatment of neuropathic corneal pain. This milestone underscores our commitment to advancing innovative therapies that can make a meaningful difference in patients’ lives. We look forward to working closely with the FDA to bring this promising treatment to patients as quickly as possible.”
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Read More on OKYO:
- Promising Developments in OKYO Pharma’s Urcosimod Program Drive Buy Rating and $7 Price Target
- OKYO Pharma Accelerates Urcosimod Development for Neuropathic Corneal Pain
- Okyo Pharma announces plans to accelerate development of urcosimod
- OKYO Pharma Achieves Key Stability Milestone for Urcosimod
- Okyo Pharma announces data on long-term stability of urcosimod
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