At Regulus, patients are at the heart of all our efforts. We work with patient advocacy organizations to enhances our ability to better understand our patients and their needs. Successful clinical trials are not possible without the participation of patients and the support of their families. We are grateful for the interest and participation in our clinical trials.
If you have any questions about our clinical trials, please speak with your physician or contact email@example.com.
Current Clinical Trials.
The following is a list of reliable resources for patients and families with reliable information related to kidney health and clinical trials.
ClinicalTrials.gov is a registry with information about the location of clinical trials, their design and purpose, and eligibility criteria. Search the database for Regulus trials or other clinical trials: www.clinicaltrials.gov
Center for Information and Research on Clinical Research Participation (CISCRP)
CISCRP is a nonprofit organization dedicated to educating and informing the public, patients, medical/research communities, the media, and policy makers about clinical research. www.ciscrp.org
The following is a list of our advocacy partners, who can provide patients and families with reliable information related to kidney health and clinical trials.
The NKF is a major non-profit health organization focused on awareness, education, prevention and treatment of kidney disease. www.kidney.org
NORD, along with its more than 300 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services. www.rarediseases.org
The PKD Foundation is a United States non-profit organization that funds research into polycystic kidney disease. It is the second-largest U.S.-based funder of PKD research after the National Institutes of Health. www.pkdcure.org
Alport Syndrome Foundation is the leading independent non-profit organization in the United States educating and giving a voice to the Alport syndrome community through education, empowerment, advocacy and research. www.alportsyndrome.org