Macimorelin
Also known as: Macrilen, AEZS-130
Key Facts: Macimorelin
- Category
- Hormonal
- FDA Status
- FDA Approved
- Clinical Status
- FDA Approved - Diagnostic for AGHD. Commercial availability uncertain: manufacturer COSCIENS (formerly Aeterna Zentaris) entered insolvency in March 2026 and surrendered Macrilen rights.
- Banned in Sport (WADA)
- Prohibited at all times under WADA S2 (growth hormone secretagogues), named on the list despite its FDA approval as a diagnostic.
- Administration
- Oral solution, fasting
- Typical Dose
- Limited community data available
- Frequency
- See research protocols
- Duration
- Single diagnostic test
How does Macimorelin work?
Macimorelin is a peptidomimetic, a small molecule built to imitate the hormone ghrelin. It binds the growth hormone secretagogue receptor (the ghrelin receptor) on the anterior pituitary, which provokes a burst of growth hormone into the blood. In a healthy pituitary that burst is large; in someone with growth hormone deficiency it stays blunted. By measuring growth hormone in blood samples drawn over 90 minutes after the drink, clinicians can tell whether the gland can mount a normal response.
What does the research show?
The approval rested on a real head-to-head validation study comparing macimorelin against the insulin tolerance test, which had long been the gold standard but is unpleasant and risky because it deliberately drops blood sugar. The macimorelin test correctly identified people with adult growth hormone deficiency about 87% of the time and correctly cleared those without it about 98% of the time, while being far simpler: one oral dose, four blood draws, no IV insulin. The standard dose is 0.5 mg/kg taken by mouth. Because it is a diagnostic given once, the safety profile is favorable, though it can prolong the QT interval on an ECG, so it should not be combined with other QT-prolonging drugs. This is a legitimately approved agent with a clear, narrow purpose, and it is not used or validated as a performance or anti-aging compound despite being a ghrelin agonist.
What doses have been studied?
Typical Dosingⓘ
Community experience
Limited community data available
See research dosing
See research protocols
Research Dosingⓘ
Scientific studies
FDA-approved diagnostic protocol
Doses from Studies
0.5 mg/kg oral single dose
Duration
Single diagnostic test
Administration
Oral solution, fasting
When and how is Macimorelin taken?
Best Time to Take
Morning or as directed
Follow recommended protocol
Food Recommendation
With or without food
Why This Timing?
Timing may vary based on individual response and goals. Consistency is generally more important than specific timing.
What are the side effects of Macimorelin?
Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.
- ●Taste changes (dysgeusia)
- ●Dizziness
- ●Headache
- ●Nausea
- ●QT prolongation
References
- https://www.healio.com/news/endocrinology/20171221/fda-approves-oral-ghrelin-agonist-for-adult-gh-deficiency-diagnosis
- https://www.research.va.gov/currents/0618-FDA-approves-new-drug-to-diagnose-adult-growth-hormone-deficiency.cfm
- https://www.medscape.com/viewarticle/890457
- https://www.hcplive.com/view/fda-approves-aeterna-zentaris-macimorelin-growth-hormone-deficiency-test
Research This Peptide Further
Frequently Asked Questions
What does Macimorelin do?
Macimorelin (brand name Macrilen) is an orally active ghrelin receptor agonist used as a diagnostic test, not a treatment. You drink a single dose, then doctors measure how much growth hormone the pituitary releases to diagnose adult growth hormone deficiency. It was FDA approved in December 2017 as the first oral diagnostic agent for that condition.
How does Macimorelin work?
Macimorelin is a peptidomimetic, a small molecule built to imitate the hormone ghrelin. It binds the growth hormone secretagogue receptor (the ghrelin receptor) on the anterior pituitary, which provokes a burst of growth hormone into the blood. In a healthy pituitary that burst is large; in someone with growth hormone deficiency it stays blunted. By measuring growth hormone in blood samples drawn over 90 minutes after the drink, clinicians can tell whether the gland can mount a normal response.
Is Macimorelin FDA approved?
Yes, Macimorelin is FDA approved. FDA Approved - Diagnostic for AGHD. Commercial availability uncertain: manufacturer COSCIENS (formerly Aeterna Zentaris) entered insolvency in March 2026 and surrendered Macrilen rights.
Is Macimorelin banned in sport?
Prohibited at all times under WADA S2 (growth hormone secretagogues), named on the list despite its FDA approval as a diagnostic.
What are the side effects of Macimorelin?
Reported side effects include: Taste changes (dysgeusia), Dizziness, Headache, Nausea, QT prolongation. Individual responses vary based on dosage, duration, and personal health factors.
What is the typical dose of Macimorelin?
Community-reported common dose: Limited community data available (See research protocols). Range: See research dosing. Administration: Oral solution, fasting. Prescription drug. Dose set by prescriber per label. Not medical advice.
Related Peptides
Peptides commonly compared with Macimorelin or used in similar applications.
Leuprolide
FDALeuprolide (brand name Lupron) is a synthetic GnRH agonist, a modified peptide far more potent than natural GnRH, and it is FDA-approved for advanced prostate cancer, endometriosis, uterine fibroids, and central precocious puberty. The clever part is counterintuitive: it works by overstimulating the GnRH system so hard that the pituitary shuts down sex hormone production. It is a real, long-established prescription drug (first US approval 1985), not a research peptide, and it carries meaningful side effects from the low-hormone state it creates.
HormonalOctreotide
FDAOctreotide is a synthetic eight-amino-acid mimic of the natural hormone somatostatin, the body's main 'off switch' for hormone secretion. It shuts down excess growth hormone, so it is a frontline FDA-approved drug for acromegaly, and it also tames the flushing and diarrhea of hormone-secreting carcinoid and other neuroendocrine tumors. This is real, approved medicine with decades of clinical data behind it, sold as Sandostatin (injectable, since 1988), Sandostatin LAR (monthly depot), and Mycapssa (oral capsule, approved 2020).
HormonalLanreotide
FDALanreotide (development code BIM-23014) is an eight-amino-acid somatostatin analog, a close cousin of octreotide, given as a long-acting deep-injection gel (Somatuline Depot/Autogel) usually once a month. The FDA approved it for acromegaly in 2007, for gastroenteropancreatic neuroendocrine tumors in 2014, and for carcinoid syndrome in 2017. Generic versions now exist alongside Ipsen's Somatuline Depot. It is established prescription medicine, not an experimental compound.
HormonalPegvisomant
FDAPegvisomant (brand name Somavert) flips the usual acromegaly strategy on its head: instead of telling the tumor to make less growth hormone, it blocks growth hormone's receptor on target tissues directly. It is a PEGylated, genetically modified version of human growth hormone that acts as a receptor antagonist, FDA-approved in 2003 for acromegaly patients who do not respond well to surgery or other drugs. It is the single most effective option for normalizing IGF-1, which is why it is a key second-line therapy.
HormonalHMG
FDAHMG (human menopausal gonadotropin, sold as menotropins under the brand Menopur) is a purified hormone mix extracted from the urine of postmenopausal women. Each standard vial carries 75 IU of FSH activity and 75 IU of LH activity, with most of the LH activity coming from hCG. It is an FDA-approved fertility drug used to stimulate egg development in IVF, and it is also used, mostly off-label in the US, together with hCG to kick-start sperm production in men whose pituitary does not make enough FSH and LH. This one has decades of real clinical use behind it.
HormonalTriptorelin
FDATriptorelin is a synthetic analog of gonadotropin-releasing hormone (GnRH) with a D-tryptophan swapped in at position 6, which makes it far more potent and longer-lasting than the natural hormone. As a long-acting depot it is FDA-approved to shut down testosterone in advanced prostate cancer (Trelstar) and to pause early puberty in children (Triptodur), and in Europe it is sold as Decapeptyl, including a short-acting 0.1 mg form used in IVF. In men's health circles it is known for something else: a single small dose used to 'restart' testosterone after steroid use. That idea rests on very little published evidence.
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