The ALXN1210 trial is recruiting participants

This phase 3 trial, which is sponsored by Alexion Pharmaceuticals, aims to…

Words Lucie van Leeuwen.Published November 17, 2020
The ALXN1210 trial is recruiting participants

This phase 3 trial, which is sponsored by Alexion Pharmaceuticals, aims to study the safety and efficacy of the drug ‘ravulizumab’ in people living with ALS. The study intends to recruit 354 adults with either sporadic or familial ALS.

The ALXN1210-ALS-308 trial is a randomised, double-blind, placebo-controlled trial. This means that the effect of ravulizumab is tested by comparing a group of patients that receive ravulizumab to a group of patients receiving placebo. Participants will be randomly assigned to receive ravulizumab or placebo. A placebo is something that looks exactly the same as the study medicine but does not have any active medicine in it. Participants are twice as likely to be assigned to ravulizumab treatment versus placebo. Ravulizumab and placebo will be administered via an injection into the bloodstream (intravenously).

The study has a randomized controlled period of 50 weeks and during this time, the participant and the research team do not know who is receiving placebo or ravulizumab.  After this period, participants can enter the Open-label Extension Period of the study and receive ravulizumab.

Key Inclusion Criteria

Key eligibility criteria for people with ALS to participate, include:

  • Disease onset within the prior 36 months
  • Documented meningococcal vaccination not more than 3 years prior to, or at the time of, initiating study treatment
  • Slow vital capacity (SVC), a measure of respiratory function, of at least 65% predicted at screening
  • If the participant is taking riluzole, he/she must be on a stable dose for 30 days
  • If the participant is taking edaravone, he/she must have been on a stable dose for 60 days
  • Body weight at least 40 kilograms at screening.
  • Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies

More information

Are you interested in participating in this trial? Please contact your local ALS Centre or treating physician. The ALXN1210-ALS-308 trial runs in ALS centres around the globe, including several TRICALS centres. You can find all participating TRICALS centres here.

For more information about the ALXN1210 trial, please refer to:  https://clinicaltrials.gov/ct2/show/NCT04248465.

TRICALS aims to speed up the development of new medicines for ALS. To effectively do that, the direct involvement of people with ALS is essential and urgent. Each person with ALS holds an important piece of the puzzle, and putting the puzzle together will help us to find new and more effective treatments.

You can help by registering with TRICALS. Click on the button below to register now!

Register

Share

Related news

Measuring treatment effects based on patient preference
Measuring treatment effects based on patient preference
To evaluate the effect of an investigational drug in ALS clinical trials, […]
TRICALS Enrols First Participants in Phase 3 MAGNET platform trial for ALS
TRICALS Enrols First Participants in Phase 3 MAGNET platform trial for ALS
TRICALS (the Treatment Research Initiative to Cure ALS), in collaboration with ALS […]
USA: new law promises $100 million for ALS research
USA: new law promises $100 million for ALS research
A new law has been passed in the United States to give […]
Congratulations to our TRICALS colleagues as UK Government invests £50 million to find a cure for ALS
Congratulations to our TRICALS colleagues as UK Government invests £50 million to find a cure for ALS
The UK government has recently announced that £50 million will be invested […]