Roidipedia.Compound reference & reporting
05 AUG 2026
CompoundsPharmaceutical Anamorelin
PharmaceuticalGhrelin receptor agonistGH secretagogueOrexigenic

Anamorelin

Also known as Adlumiz · ONO-7643 · RC-1291 · ANAM

Orally active ghrelin-receptor agonist developed for cancer cachexia. It increases appetite, lean body mass and body weight, and is approved in Japan for cachexia in several cancers, though it did not improve handgrip strength in trials.

01 Overview

Anamorelin (brand Adlumiz/Rayaldee-unrelated; JMT-101) is a selective agonist of the growth hormone secretagogue receptor that mimics ghrelin's orexigenic and anabolic signalling. In the ROMANA phase 3 programme it consistently raised lean body mass and appetite in patients with non-small-cell lung cancer cachexia.

It is approved in Japan for cancer cachexia in NSCLC, gastric, pancreatic and colorectal cancer, but was not approved in the US or EU because the co-primary endpoint of handgrip strength was not met. It is orally dosed and generally well tolerated.

02 Mechanism

Agonist at the ghrelin/GHSR-1a receptor, driving GH/IGF-1 secretion and central appetite stimulation, producing anabolic and orexigenic effects.

03 Dosing

TierDoseRouteNotes
Cachexia dose100 mg/dayOralOnce daily on an empty stomach, as studied in ROMANA and Japanese trials.

04 Effects

EffectMagnitudeEvidence
Increased lean body massConsistently raised lean body mass in NSCLC cachexia trials.+1.1 kg vs placebo over 12 wkClinical
Improved appetiteGhrelin-mimetic appetite stimulation improved anorexia-cachexia symptom scores.significant vs placeboClinical
No handgrip strength gainDespite mass gains, functional strength did not improve significantly.endpoint not metClinical

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
HyperglycaemiaElevated blood glucose and HbA1c, reflecting GH/IGF-1 axis activation.ModerateCommonClinical
NauseaMild GI upset early in treatment.MildCommonClinical

07 References

Anamorelin in advanced NSCLC cachexia (ROMANA 1 and 2)Lancet Oncol, 2016

08 Discussion0 comments

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