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Critical Research Limitation: Despite extensive preclinical and limited early-phase human studies, the CJC-1295 (NO DAC) + Ipamorelin blend peptide has NO completed, peer-reviewed Phase III clinical trials establishing human safety and efficacy for any medical indication
neuropathy), effective replacement therapy should lead to a normal full blood count and B12 level after 8 weeks of treatment, while improvement in neurological symptoms begins very quickly within one week of initiation of therapy but can take up to 3 months to resolve (Carmel, 2008)
Pediatric patients 10 years of age and older: 10 mg subcutaneously once weekly
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