Clinical Trials

If you or a loved one has ALD/AMN, you know the heartbreaking frustration that there are not many treatments that can stop or significantly slow the all forms of the disease. You may not know that there are hundreds of scientists and doctors working hard to discover those treatments. That discovery depends, in large part, on the willing spirit of people with ALD/AMN who volunteer to be a part of a clinical trial.

Clinical research is the only way that promising science will become treatments and cures for ALD/AMN. Patients and caregivers are all incredibly important to this process. ALD Connect is committed to providing accurate, up-to-date information for all stakeholders in the clinical research process.

Clinical Trials for ALD/AMN

clinicaltrials.gov is a central database of clinical trials for medical disorders of all kinds, including ALD/AMN. It is an important resource for finding a clinical trial that is right for you. The site is maintained by the National Library of Medicine, a branch of the US government.
Click here to see all ALD and AMN trials.
Click here to search the database using your own search terms.

Clinical Trials 101: Placebo-Controlled Trials

Most ALD/AMN patients and caregivers want to do everything they can to help find new treatments for the disease. The idea of trying an experimental therapy is often regarded positively, despite knowing that risks may be present. However, some people have misgivings when they learn that some participants in a trial may receive a placebo rather than the drug being tested.

Drawn to Science: Clinical Trials Video

Produced by Roche.

Participating in a Clinical Trial

People with ALD/AMN who enroll in a clinical trial are contributing to improved health care for everyone with the disease. Even when the results of a trial are negative, we learn that much more about the disease, and how to look for more promising new treatments.

What should patients and their families consider before participating in a trial?

Patients and their families should learn as much as possible about the clinical trial before signing a consent. The following questions might be helpful for the participant to discuss with the health care team. Some of the answers to these questions are found in the informed consent document.

We recommend visiting the Center for Information and Study on Clinical Research Participation (CISCRP) webpage for additional educational material on clinical trials. CISCRP is an independent non-profit organization dedicated to educating and informing the public and patients about clinical research. CISCRP also provides information and resources to help research and health professionals better serve their patients and study volunteers. CISCRP has excellent educational videos on their website which illustrate some best practices for clinical trial participants. Click here to see the videos.