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Improves sleep quality and deep recovery Supports lean muscle development Enhances fat loss and body composition CJC-1295: GHRH analog binds pituitary GHRH receptor for extended GH release Ipamorelin: selective GHS-R1a agonist amplifies GH pulse with minimal cortisol/prolactin Dual-pathway synergy produces pulsatile GH release mirroring physiological patterns Increases IGF-1, collagen synthesis, lean mass Decreases adiposity Enhances libido and sexual desire Works for both men and women Improves sexual performance and satisfaction MC3R/MC4R agonist in hypothalamus central CNS mechanism, not vascular like PDE5-i Works independently of hormone levels effective even with normal testosterone FDA-approved as Vyleesi for HSDD in premenopausal women Off-label in men Onset 12 hours Peak effect 23 hours Duration 612 hours Mechanism: PT-141 activates melanocortin receptors in the hypothalamus via the CNS dopaminergic reward pathway directly stimulating sexual desire

Based on your lab results and clinical picture, Dr