As a mucolytic with antimicrobial properties, cysteamine can potentially help patients with all CF mutations.
Studies have shown CFTR rescue in patients who are homozygous for the F508del mutation. Rescue may not be limited to these mutations, but further studies are warranted before any assumptions can be made.
New research and clinical trials are showing real promise for the use of cysteamine for the treatment of cystic fibrosis. Since much of the research regarding cysteamine for CF is very new, this blog has been created as a resource for CF patients and caregivers who want to know more. Disclaimer: Please consult your physician before attempting to use any of the medications listed on this site. For informational purposes only.
- What is it and Why Cysteamine for CF?
- Cysteamine + CF -- Research Links
- Cysteamine Clinical Trials
- What CF Mutations Can Benefit from Cysteamine?
- Cysteamine--Brands, Cost, Availability
- Why EGCG with Cysteamine for CF?
- EGCG--Brands, Cost, Availability
- Dosing (Cystagon / EGCG)
- Cystagon Side Effects/Contraindications
- Case Studies
- In the News
- About CF
- Credits
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