The ME Association believed that the drug Rituximab represented the most important development so far in terms of a potential disease altering treatment for at least a sub-group of people with ME/CFS.

This was until we heard the discouraging news from the phase III clinical trial in Norway at the end of 2017 (see below).

We had set aside a specific amount of funds for a clinical trial of Rituximab in the UK and were willing to consider all high quality research applications.

As it is we await the formal publication of the Norwegian clinical trial results (not yet published but expected shortly and will then determine the best course of action moving forward (as at Sept. 2018).

News and progress reports:

  • 2017 Latest: Negative results from the phase III Rituximab trial. The clinical trial is still expected to be published in early 2018, but preliminary negative results were revealed at a conference in Norway by Dr Olav Mella, on 21st November: see ME Association statement.
  • 2017: The current plan regarding any UK clinical trial of Rituximab would appear to be to wait for publication of the Norwegian phase 3 clinical trial, which is now expected in 2018. It also appears that the chosen site for a UK trial, which could begin in 2018 if the results from Norway are favourable, will be in Norwich – with patients being recruited from Norfolk and Suffolk.
  • June 2016 – Invest in ME held their annual research conference which included a presentation from Dr Jo Cambridge who talked about B-cell biology and Rituximab treatment. The conference report from Dr Charles Shepherd features highlights from this and other presentations.
  • May 2016 – Following a public meeting in Sussex with Dr Amolak Bansal about Rituximab, MEA medical advisor Dr Charles Shepherd posted an update on the proposed UK trial.
  • September 2015 – MEA trustees issued a position statement relating to the £60,000+ it has ring-fenced for any suitable UK clinical trial of Rituximab. The statement also features the necessary application conditions for any clinical trials research group who are proposing to perform a clinical trial.

Background to Rituximab and M.E.

The ME Association has consistently maintained that the positive results emanating from Drs Fluge and Mella – coming first from the 3-patient Preliminary Case Series in 2009, and followed by the 30-patient Phase II Double-blind and Placebo-controlled Trial in 2011 reporting a strong and lasting improvement in 67% patients (and 13% of placebo controls) – demonstrated that Rituximab had exciting potential as a possible treatment for at least a sub-group of people with ME/CFS.

Leaflet on Rituximab – Jan 2018 (click to access).

These initial studies were followed by an Open-label Phase II Study from the same Norwegian team, who wanted to see what the optimal dose of Rituximab might be and if this maintenance dose would also have a lasting effect on those treated.

29 people with ME/CFS were included in this study and all of them, with the exception of one, had been in the 2011 study. Those that had received the placebo in the last study were this time treated with Rituximab.

Published in July 2015, this open-label study successfully produced additional evidence that Rituximab was very effective for a significant proportion (64%) of those with ME/CFS over the medium term (up to 36 months), and with very minor reported side-effects.

However, as an open-label study it was not blinded – patients knew they were receiving Rituximab and that it had previously demonstrated benefit, which could have affected the reported benefits – and there was no control group. Also, as mentioned above, the study did not employ new patients; it relied on those who had been in the previous trial.

It should also be noted that those few patients considered very severely affected – bedbound – in this latest study were deemed ‘non-responders’ to the drug, which would seem to match previous observations for this patient group; although Drs Fluge and Mella plan to conduct a separate study to try and discover why this might be the case.

Despite the generally positive results, the authors continue to express necessary caution:


“We do not encourage the use of Rituximab for ME/CFS outside of approved clinical trials, and this is especially important for the group with very severe disease.”

The main purpose of this 2015 study was to help the researchers’ with the much larger multi-centre Phase III trial, which is currently underway and has been financed by the Norwegian Government and private donations. This gold-standard randomised placebo-controlled trial (RCT) will recruit 152 patients and follow their progress for 24 months after they have received treatment.

The results – expected in 2018 – will represent the most significant yet and could provide further incentive to central funding bodies in other countries to attempt equally large replication studies.

(Note: See update above re: failure of Rituximab. As at Sept. 2018 we are still awaiting final publication which will allow an analysis of the failed trial.)

What might Rituximab mean to M.E. and possible disease mechanisms?

The Norwegians were clear from the start that they felt the positive results from treatment could mean a sub-set of people with ME/CFS were struggling with some form of autoimmune disease process.

They reiterated this position in their 2015 paper:


The observed patterns of delayed responses and relapse after B-cell depletion and regeneration, a three times higher disease prevalence in women than in men, and a previously demonstrated increase in B-cell lymphoma risk for elderly ME/CFS patients, suggest that ME/CFS may be a variant of an autoimmune disease.”

However, the method by which Rituximab appears to be a safe and effective form of treatment for some people with ME/CFS remains uncertain, and establishing precisely how it works is another aspect to the research on this drug that needs to be completed.

Note: An autoimmune disease occurs when the body’s immune system starts producing harmful antibodies – autoantibodies – which are directed against the body’s own tissue. There is some evidence to indicate that low levels of some autoantibodies are present in some people with ME/CFS. In our current state of knowledge, this is best described as saying that there may be an autoimmune component in some cases of ME/CFS. However, we are not yet in a position to say that ME/CFS is an autoimmune disease.

The Christmas Appeal

More research for M.E. in 2019

We believe that biomedical research offers the best hope. And we want to fund more research in 2019 than ever before. Please help us to build on our success and continue to expand our vital work.

If you would like to help our Christmas Appeal, please donate:

  • with a single online donation via JustGiving, or,
  • by cheque (made payable to: The ME Association) to: The ME Association, 7 Apollo Office Court, Radclive Road, Gawcott, Bucks MK18 4DF, or,
  • by card donation over the phone to our head office (01280 818964).

If you would like to fundraise for the Christmas Appeal, please start your online giving page, here.

One day we will find the cause of this disease and have effective forms of treatment. And with your help, that day could come much sooner.

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