RE: Fantastic Day30 Oct 2025 19:07
Are people confusing FDA approval with Opran status, we are a long way from FDA approval.
• Scenario A (ODD granted + positive partnering/licensing deal):
If the FDA grants ODD (which would be an incremental piece of news) and Nuformix announces a licensing deal (say upfront + milestones) for NXP002, the share price could see a moderate “re‐rating” boost. For example, shares might rise by 20-50 % (depending on prior valuation, market sentiment, liquidity) as the company’s risk profile and commercial potential increase.
• Scenario B (ODD granted + successful early clinical data + major licensing or partner):
If in addition to ODD they publish good early data and secure a major partner, the share could rise substantially – perhaps 50-100 % or more — because the pipeline is de-risked and commercial path clearer.
• Scenario C (Full FDA approval):
This is a transformational event. If NXP002 gets FDA approval for IPF/related fibrosis, the share price could move dramatically (potentially multiples above current) provided the market sees the pathway to revenue and profitability. How big depends on the indication size, pricing, competition, and the deal terms. For a rare disease asset with exclusivity, valuations can go high. But there’s no standard multiplier — could be 2-5× or more, or less if issues arise.
• Scenario D (Negative outcome / delay):
On the flip side, if the FDA denies ODD, or trials fail, or commercial prospects look weak, share price could drop significantly (perhaps 30-70 % or more), especially given the speculative nature of the company.