France-based Nicox develops therapeutics for the treatment of ocular conditions. Lead candidate NCX-470 is in Phase III studies for the treatment of glaucoma and it is advancing NCX-4251 for dry eye disease. Nicox receives licence revenue for its FDA-approved drugs Vyzulta and Zerviate.
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Andreas Segerros
CEO
Gavin Spencer
Executive VP and Chief Business Officer
Michele Garufi
Chairman
Forecast net debt (€m)
9.2
Forecast gearing ratio (%)
26
% | 1M | 3M | 12M |
---|---|---|---|
Actual | (16.4) | 24.4 | (42.2) |
Relative | (11.7) | 29.2 | (41.8) |
52 week high/low | €0.4/€0.2 |
Nicox has reported that an in vivo study carried out in beagles found that NCX-470 (0.1%) treatment led to a greater degree of intraocular pressure (IOP) reduction compared to AbbVie’s Lumigan (bimatoprost 0.01%), the best-selling branded prostaglandin F2α analogue (PGA) drug, in both single and repeated (five-day) dosing. The newly reported data from the open-label cross-over study assessing NCX-470, Lumigan and vehicle were published in the peer-reviewed Journal of Ocular Pharmacology and Therapeutics. While we acknowledge the limitations in read-across from animal data and note the Mont Blanc study did not show statistical superiority against PGA drug latanoprost (although it did meet the non-inferiority primary efficacy endpoint), we believe the new findings add to the body of collective data suggesting a competitive commercial profile for NCX-470 versus standalone PGA drugs such as bimatoprost.
Y/E Dec | Revenue (€m) | EBITDA (€m) | PBT (€m) | EPS (fd) (c) | P/E (x) | P/CF (x) |
---|---|---|---|---|---|---|
2021A | 8.6 | (16.5) | (15.5) | (31.74) | N/A | N/A |
2022A | 5.2 | (21.1) | (18.3) | (33.68) | N/A | N/A |
2023E | 6.1 | (16.4) | (15.6) | (31.19) | N/A | N/A |
2024E | 7.6 | (18.0) | (20.3) | (40.50) | N/A | N/A |