Overview
Anamorelin is an orally active ghrelin receptor agonist developed for cancer cachexia, approved in Japan for non-small-cell lung cancer cachexia.
- Approved pharmaceutical (Japan)
- Oral tablet
Mechanism of action
Mimics ghrelin to stimulate appetite, lean body mass, and GH/IGF-1 axis in catabolic states.
- · GHSR-1a
- · GH and IGF-1 axis
- · Appetite regulation
- · GH
- · IGF-1
- · Ghrelin
How it acts on the body
Anamorelin combines two effects useful in cancer cachexia — appetite stimulation and direct GH/IGF-1-mediated anabolic support — in an oral formulation. In phase 3 trials it increased lean body mass and appetite in NSCLC cachexia, leading to Japanese approval.
It does not consistently improve handgrip strength or survival, which kept it out of US/EU labeling, but the lean mass and appetite signals remain meaningful for symptom management.
Hormonal & endocrine impact
How this peptide is reported to shift specific hormones and signaling molecules. Directionality reflects research literature and preclinical models, not clinical prescribing data.
Curves are schematic shapes (sigmoid for increases/decreases, damped oscillation for modulation/stabilization) anchored to a 100% baseline. They communicate direction and tempo of change reported in research literature — not absolute hormone concentrations.
Effects on the body
Organ system effects
Anabolic support in catabolic states.
GH/IGF-1 axis stimulation.
Appetite stimulation.
Reported effects
Drawn from preclinical research, anecdote, and small-scale clinical observation. No evidence grades are assigned — most peptides on this page lack rigorous human trials.
- Oral dosing
- Combined appetite and anabolic mechanism
Potential side effects
- · Hyperglycemia
- · Diabetes diagnosis or worsening
- · Hepatic enzyme elevation
- · Cardiac conduction concerns in early trials, not a major label signal
Drug interactions
Pairing context
- Nutritional support and resistance exercise as toleratedMaximizes lean-mass response.
- Uncontrolled diabetesMay worsen glycemic control.