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While the petitions grievances are specific to peptides, they reflect long-running criticisms of the FDA, which has often come under fire from patient advocacy groups who want better access to experimental treatments that might ease the progression of deadly diseases
To do otherwise will interfere with the slow release of this drug, and make it less effective
In 2023 the FDA placed CJC-1295 in "Category 2" of its interim 503A bulks list, meaning it identified significant safety concerns and did not permit its use in traditional pharmacy compounding
Approaches may include physical therapy, interventional pain management, and less-invasive procedures using Regenexx injectates designed to help manage symptoms and improve function
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