C3 Glomerulopathy Resources | WeC3G.com

Use these resources to help guide you on your C3G journey. Check back regularly for additional tools and updates.


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C3G Natural History Study

A natural history study tracks the course of a disease over time. The goal of this type of study is to collect information about disease progression that will inform research and the development of new medicines and treatments.

There is a multinational natural history study of C3G in progress called, "Natural History Study of C3 Glomerulopathy (C3G): Discovery of Histological Predictors of Outcome." It is being led by Imperial College London. The study is expected to be 3 years in length and will involve 400 participants, with results to be shared publicly.

Achillion Pharmaceuticals, Inc. is a sponsor of this study.

For more information, check out the study website.

You can also follow on Facebook and Twitter.

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Patient-Focused Drug Development Meeting

There are times when patients, caregivers, and doctors who are experts in a certain disease formally come together to discuss what it is like to live with the disorder. These meetings are called Patient-Focused Drug Development (PFDD) meetings. They inform companies, organizations, and regulatory authorities about the patient perspective on a disease and its treatments, and can help support making new medicines available to patients.

In August 2017, a PFDD in C3G disease was led by the National Kidney Foundation with participation from the United States Food and Drug Administration (FDA). Learn more about the meeting and patient perspectives shared there here. This meeting was sponsored by Achillion Pharmaceuticals, Inc.

Read the "Voice of the Patient" report summarizing the meeting.

Watch the video.

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Clinical Trials

Clinical trials are carefully conducted research studies to help physicians better understand and treat disease. There are investigational treatments for C3G that are currently being studied in ongoing trials.

Learn more about how clinical trials work and find ongoing studies in your area. Be sure to check back often, as new studies may become available.

Learn more about trials.


Organizations and Websites

Here is a list of helpful organizations and links to their websites:

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WeC3GTM Toolkit

Get access to even more resources and tools when you join the WeC3G community.

  • Customizable Information Letters: Letters for patients or caregivers of patients with C3G to give to teachers, school nurses, coaches, or others to help educate them about the condition and set appropriate expectations
  • Key Facts About C3G: Visual guide for understanding C3G and how it impacts the body
  • Living With C3G Guide: Helpful information for patients with C3G
  • C3G Doctor Discussion Guide: Discussion points for you and your loved ones to download and to help prepare you for partnering with your care team
  • C3G Awareness and Advocacy Guide: Information, ideas, and resources to help raise awareness and build advocacy

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Learn more about managing C3G now and in the future.

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