VialFacts DeutschSvenska

Claims on this page checked 2026-08-26

Tabimorelin

PMID 12699438 reports that 9 of 83 adults with growth hormone deficiency reached a peak GH of at least 5 µg/L after the first and/or final NN703 administration (checked 2026-08-26). No placebo participant reached that threshold (0 of 14). The opened PubMed record lists no grant. The corresponding Crossref record lists no funder. The PubMed record's affiliation is Sahlgrenska University Hospital. This was a one-week response study, not a long-term outcome trial.

What exactly is Tabimorelin?

Tabimorelin was studied as NN703. The human papers call it an orally active growth hormone secretagogue and examine pharmacodynamics and pharmacokinetics. A cell and animal paper reports action at GHS receptor 1A (PMID 10427162; checked 2026-08-26).

Identity fieldVerified value
Register nameTabimorelin
Register classGrowth hormone secretagogue receptor 1A agonist; orally active ghrelin mimetic (PMID 10427162; PMID 33458843; checked 2026-08-26)
Register aliasNN703
Other GSRS namesNN-703; NNC-26-0703
GSRS substance classChemical
Molecular formulaC32H40N4O3
Molecular weight528.6862
UNIIL51CBE03KF
Register CAS193079-69-5
Other CAS in the same GSRS record249762-09-2
Identity sourceGSRS Tabimorelin record, checked 2026-08-26
Related register recordsIpamorelin; MK-677; Macimorelin

What did direct human studies measure?

The human records examine short GH responses, pharmacokinetics, and one CYP3A4 interaction. No trial here tested a long-term health outcome.

Primary recordHuman sampleMeasured findingFunding and limit
PMID 1269943897 adults with GH deficiency; 83 NN703 and 14 placebo9 of 83 (11%) reached peak GH ≥5 µg/L after the first and/or final NN703 administration. Placebo had 0 of 14 responders. The initial GH difference lost significance after adjustment for BMI. After one week, GH peak and area under the curve were similar between groups. IGF-I was unchanged. IGFBP-3 rose versus placebo after BMI adjustment (p<0.05).PubMed lists no grant. Crossref lists no funder. The PubMed affiliation is Sahlgrenska University Hospital. One-week response study. Checked 2026-08-26.
PMID 11032702Healthy men; count not stated in this abstractGH area under the curve was higher than placebo at the three highest tested levels. Peak GH was higher at the four highest tested levels. IGF-1 was higher at the two highest tested levels (p<0.0001). The abstract also notes subtle individual changes in ACTH, cortisol, and prolactin at higher tested levels.PubMed lists no grant. Crossref lists no funder. The PubMed affiliation is Novo Nordisk A/S. Single-dose study; no adverse-event count or rate. Checked 2026-08-26.
PMID 112103968 dose groups; each had 6 active and 2 placebo participantsA pharmacokinetic model estimated 485 ng/mL for half-maximal GH stimulation. The model also included a threshold and development of tolerance.PubMed lists no grant. Crossref lists no funder. The PubMed affiliation is Novo Nordisk A/S. Single-dose modeling study. Checked 2026-08-26.
PMID 11437473Healthy men; count not stated in the opened abstractGH area under the curve and peak GH rose with tested level on days 1 and 7. Overall GH release decreased from day 1 to day 7 (p<0.001). IGF-I rose more than placebo at the three highest tested levels. IGFBP-3 rose more at the highest tested level. The abstract also reports isolated changes in prolactin, TSH, ACTH, and cortisol.PubMed lists no grant. Crossref lists no funder. The PubMed affiliation is Novo Nordisk A/S. Seven-day study; no adverse-event count or rate. Checked 2026-08-26.
PMID 1261074517 adult menMidazolam area under the curve rose 64% after one NN703 exposure and 93% after repeated exposure; p=0.0001 for both comparisons. It remained 45% above baseline after washout (p=0.0001).PubMed lists no grant. Crossref lists no funder. The PubMed affiliation is Novo Nordisk A/S. Drug-interaction study, not a GH treatment result. Checked 2026-08-26.

Two abstracts say NN703 was well tolerated. They give no event count or rate.

One study found that the drug changed midazolam exposure.

How strong is the evidence?

Tier B means short human studies are available (checked 2026-08-26). The tests lasted one dose or one week. They measured GH, drug handling, or a drug interaction. None reported a long-term health result.

What do current United States product records show?

Exact search checked August 26, 2026ResultBoundary
DailyMed: Tabimorelin; NN703No current labelExact terms only
openFDA Drugs@FDA: Tabimorelin; NN703No matching applicationDoes not settle another place or time

What do the central EU and country fields show?

FieldCurrent primary record
Central EU status: unclearEMA report generated August 26, 2026: 2,732 medicine rows; no Tabimorelin, NN703, or NN-703 row. Positive controls resolved. The central file does not cover every national authorization.
Germany: doping_classifiedThe DmMV annex names Tabimorelin under growth hormone secretagogues (GHS) and their mimetics. This classification is separate from evidence tier and authorization. Checked 2026-08-26.
Sweden: unclearProduct file dated August 26, 2026: 38,382 rows; no Tabimorelin, NN703, or NN-703 row. Positive controls: semaglutide 44, tirzepatide 18, somatropin 132, teriparatide 18. This exact-name result does not classify a product under another name.

When was Tabimorelin first observed in circulation?

The register stores first_observed: null.

No dated circulation record is claimed. The field stays empty instead of being guessed.

What does the large submitted-vial study show?

Submitted-vial paperResult
2026 preprint, DOI 10.20944/preprints202604.1748.v1Lists fourteen compounds; Tabimorelin is absent. Checked 2026-08-26.
Tabimorelin resultNo identity, amount, purity, or endotoxin finding. No first-observation date.

What vial testing can show

All compounds in the register