Roidipedia.Compound reference & reporting
05 AUG 2026
CompoundsPharmaceutical Tabimorelin
PharmaceuticalGhrelin receptor agonistGH secretagogue

Tabimorelin

Also known as NN703 · NNC 26-0703

Orally active ghrelin-receptor agonist studied for adult GH deficiency and as a GH secretagogue. Development was discontinued after chronic dosing showed liver enzyme elevations and CYP3A4 induction.

01 Overview

Tabimorelin (NN703) is a peptidomimetic GHSR-1a agonist that raises GH and IGF-1 after oral dosing. It was investigated for adult GH deficiency and as an anabolic secretagogue in the early 2000s.

Chronic administration produced elevations in liver transaminases and induction of CYP3A4, and development was ultimately abandoned. Its human data are limited to small early-phase studies, so its research base is modest.

02 Mechanism

Agonist at the ghrelin/GHSR-1a receptor promoting pituitary GH release; also crosses into peripheral tissues.

03 Dosing

TierDoseRouteNotes
Investigational0.5–5 mg/kg/dayOralDoses used in discontinued early-phase studies; not approved.

04 Effects

EffectMagnitudeEvidence
Raised GH and IGF-1Increased GH and IGF-1 after oral dosing in short trials.dose-dependentClinical
Orally activeEffective by mouth, unlike injectable GHRP peptides, an advantage that motivated its development.peptidomimeticClinical

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
Elevated liver enzymesTransaminase elevations on chronic dosing halted development.ModerateCommonClinical
Drug interactions via CYP3A4Induces CYP3A4, altering metabolism of co-administered drugs.ModerateUnknownClinical

07 References

Tabimorelin (NN703), an orally active GH secretagogueEur J Endocrinol, 2004

08 Discussion0 comments

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