Neuralzeta efficacy

Provided free of charge by a voluntary charity
Stability (i.e., disease progression stopped):
16% stable for < 4 months
27% of patients stable for 4 months
22% stable for 6 months
19% stable for one to nine years
 No other drug has ever achieved this. For 16% of patients the drug has no effect i.e., non responders (Data source: Patients own monitoring reports observed by their neurologists).

12,000 doses, 128 years of accumulated patient-treatment, more than 28,000 datum points. This is profoundly more safety and clinical evidence of efficacy than any of the recently FDA approved drugs. Neuralzeta treatment continues and is ongoing.

Developed and supplied free of charge by a small informal charity on a first come first served basis with no exclusion criteria as a humanitarian endeavour when funding is available. The charity has never asked anyone for money at any time.

The objective is to get it approved and supplied at cost price.
This is in stark contrast to the recently approved ALS drugs: Toferson ($16,580 per month), Relyviro ($13,166 per month) and Edaravone ($14,083 per month) - none of which extend life. (Source: Biospace.com  April 25th 2023)

Kindly study `Important information`, in the black section at bottom of this page. 

Important information

Based in Europe, the RC Charity has no connection with any other entity, charity or corporate, and has no external financial support. Being privately funded by three persons and run by a voluntary unpaid trustee, and the public nor any ALS victim have ever been asked for money, there is no requirement to register ​​the charity and incur the associated administrative costs (Registration, trustees, auditing etc.).

The humanitarian objective is to bring a potentially new horizon to those affected by ALS (also known as MND) - irrespective of their financial status. Provided free of any charge on first come first served basis (when funds are available) to any MND/ALS victim who asks for help, only subject to having a credible case history, a confirmed diagnosis, informed patient consent and a valid prescription from a neurologist or medical doctor.

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As a many years are covered in this site, precise data statistics vary at different times. This site is published about once per year. 2016 ALSTDI page added. 2017 Edavarone comparison page. 2020 Efficacy chart updated, 2021 Family 127 added. 2022 ALSFRS-R added. ​​​ ​​

NOTE: Nothing in this web site may be considered to be medical advice. You must always consult with your neurologist or doctor.

There is another registered domain: www.RCH4als.com, intended to provide information for those diagnosed with ALS/MND and is voluntarily sponsored by PALS around the world treated with RCH4. You may wish to join that group. That web site has no connection with us, however use of the drug name `RCH4` in that domain name is used with the permission of this charity.
Further independent RCH4 patient experience, comment & information is available at Patients Like Me ​

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