Nurexone Biologic

Nurexone Biologic FCF Conversion

The FCF Conversion Rate (FCF/EBITDA) of Nurexone Biologic (NRX.V) as of Oct 31, 2026 is 71.52 %. In the previous year, FCF Conversion Rate (FCF/EBITDA) was 109.80 % — a change of -34.86% (lower).

FCF Conversion

71.52 %

YoY

-34.86%

Last updated:

FCF Conversion Rate (FCF/EBITDA) of Nurexone Biologic is 2025 71.52 % . FCF Conversion Rate (FCF/EBITDA) of Nurexone Biologic was 2024 109.80 % . It decreases by -34.86% lower compared to the previous year.

The Nurexone Biologic FCF Conversion history

  • 3 Years

  • 10 Years

  • 25 Years

  • Max

FCF Conversion
Date
FCF Conversion
Jan 1, 2018
140.00 USD
Jan 1, 2019
166.67 USD
Jan 1, 2020
0.00 USD
Jan 1, 2021
74.80 USD
Jan 1, 2022
47.74 USD
Jan 1, 2023
84.12 USD
Jan 1, 2024
109.80 USD
Jan 1, 2025
71.52 USD
The Nurexone Biologic FCF Conversion history
YEARFCF ConversionYoY
71.52 %-34.86%
109.80 %+30.53%
84.12 %+76.19%
47.74 %-36.18%
74.80 %—
0.00-100.00%
166.67 %+19.05%
140.00 %+138.38%
58.73 %-11.90%
66.67 %-51.52%
137.50 %+140.63%
57.14 %—

Access this data via the Eulerpool API

100,000 free requests/mo · no credit card

Nurexone Biologic Stock analysis

What does Nurexone Biologic do? NurExone Biologic, Inc. develops and commercializes biological extracellular vesicles (EV)-based technology, focusing on ExoTherapy, an exosome therapy production platform for global markets. The company is developing ExoPTEN, its first ExoTherapy-based product targeting acute Spinal Cord Injuries (SCI), aiming to reverse or reduce paralysis through exosomes, membrane-bound extracellular vesicles. The firm targets conditions like SCI, Brain Trauma Injury (BTI), and other neurological indications, pending FDA approval after clinical trials. The company generates revenue through the development and commercialization of its ExoTherapy platform and ExoPTEN product, selling these to healthcare providers, hospitals, and potentially pharmaceutical partners in the global market. ExoPTEN is positioned as a treatment for acute SCI, with potential expansion into BTI and other neurological conditions once approved. The primary market segments include patients with SCI, BTI, and neurological disorders seeking advanced therapeutic solutions. NurExone Biologic, Inc. relies on FDA approval following successful clinical trials to monetize its technology. The company’s revenue model centers on the sale of ExoTherapy-based products, with ExoPTEN as the flagship offering. The global market for neurological treatments, particularly for SCI and BTI, represents the key commercial segment for the firm’s technology and products. Nurexone Biologic is one of the most popular companies on Eulerpool.

Frequently Asked Questions about Nurexone Biologic stock

FCF Conversion Rate (FCF/EBITDA) of Nurexone Biologic is 71.52 % in 2025.

FCF Conversion Rate (FCF/EBITDA) of Nurexone Biologic changed from 109.80 % to 71.52 %, representing a -34.86% change. The value is lower than the previous year.

On Eulerpool you can find the complete historical development of FCF Conversion Rate (FCF/EBITDA) Nurexone Biologic since 2006 – with annual values, charts, and detailed analysis.

FCF conversion measures how effectively EBITDA converts to free cash flow. Higher conversion indicates efficient capital allocation and low maintenance costs.

A 'good' varies by industry and company stage. On Eulerpool, you can compare FCF Conversion Rate (FCF/EBITDA)'s Nurexone Biologic with sector peers and the industry average to assess whether it is attractive.

To evaluate FCF Conversion Rate (FCF/EBITDA)'s, it is essential to compare it with peers in the same industry and sector. On Eulerpool, you can find direct industry comparisons for FCF Conversion Rate (FCF/EBITDA).

Access this data via the Eulerpool API

100,000 free requests/mo · no credit card

Cash Flow — Nurexone Biologic

All Key Metrics — Nurexone Biologic