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Both flagged some examples as posing potential legal risks, under statutes that limit the claims health care providers can make about drugs that are not FDA-approved

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Randomised, double-blind, placebo-controlled dose-escalation studies show that CJC-1295 produces sustained, dose-dependent increases in growth hormone and IGF-1, lasting several days after subcutaneous administration.[18] Ipamorelin has published human pharmacokinetic and pharmacodynamic data,[19] and has undergone a randomised phase-II study for postoperative ileus after bowel surgery.[20] But endocrine activity is not a dermatological outcome

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A company proposes TABA as part of its overall cost-based maximum which must be built into proposals, rather than requested separately

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