OKYO Pharma (OKYO) Q4 2025 earnings summary
Event summary combining transcript, slides, and related documents.
Q4 2025 earnings summary
11 Jun, 2026Executive summary
Clinical-stage biopharma focused on inflammatory eye diseases and ocular pain, with lead candidate urcosimod targeting ChemR23 for neuropathic corneal pain (NCP) and dry eye disease (DED).
Urcosimod received FDA Fast Track designation for NCP in May 2025; Phase 2 NCP trial showed promising pain reduction but was underpowered due to early closure after 18 patients.
No product revenue to date; operations funded by equity and convertible debt.
Financial highlights
Net loss for FY ended March 31, 2025: $4.7M, a significant improvement from $16.8M in FY 2024.
R&D expenses decreased to $2.3M (from $8.2M in FY 2024) due to completion of DED trial and smaller NCP trial.
General and administrative expenses fell to $4.8M (from $7.5M in FY 2024), reflecting lower bonuses, insurance, and consultancy costs.
Cash and cash equivalents as of March 31, 2025: $1.6M; working capital deficit: $5.6M.
Accumulated deficit: $143M as of March 31, 2025.
Outlook and guidance
Company expects continued significant losses and negative cash flows as clinical development progresses.
Additional capital required to fund ongoing and future trials; recent $2.7M raised post-year-end via ATM facility.
Substantial doubt exists about ability to continue as a going concern without further financing.
Latest events from OKYO Pharma
- Urcosimod achieved >80% pain reduction in 75% of NCP patients and advances to Phase 3.OKYO
Investor presentation20 Jul 2026 - Advanced urcosimod for NCP to Phase 3, raised $20M, and reported a $8.95M net loss for FY2026.OKYO
Q4 202620 Jul 2026 - Net loss widened to $16.8M as clinical progress advances, but funding remains critical.OKYO
Q4 202411 Jun 2026 - Biopharma aims to raise $200M to advance urcosimod for eye pain, facing high risk and funding needs.OKYO
Registration filing11 Jun 2026