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Evidence: HighPeptideFDA ApprovedSynthetic ACTH 1-24FDA-approved 1970 · CortrosynAdrenal test

Tetracosactide

The synthetic ACTH fragment behind the standard test of adrenal function

Tetracosactide is the first 24 amino acids of ACTH, made synthetically, which is all the hormone needs to stimulate the adrenal glands. In the US, as Cortrosyn, it is the standard diagnostic test for adrenal insufficiency; outside the US a long-acting depot form treats infantile spasms.

Overview

What is it?

Adrenocorticotropic hormone (ACTH) is made by the pituitary gland and tells the adrenal glands to produce cortisol. Its activity sits in the first part of the molecule: the Cortrosyn label notes that amino acids 1 to 20 are the minimum needed for full activity, and that shortening the chain further quickly destroys it. Tetracosactide, also called cosyntropin, is a synthetic copy of the first 24 amino acids, and 0.25 mg stimulates the adrenal cortex as fully as 25 units of natural ACTH.

Its main use in the US is diagnostic. In the short stimulation test, blood cortisol is measured before an injection and exactly 30 and 60 minutes after; a weak rise points to adrenal insufficiency. Researchers have tested simpler ways to give it: a nasal spray with chitosan produced plasma cortisol at 60 minutes equivalent to the standard intravenous test, and in people on haemodialysis the test gave equivalent results during a dialysis session.

Outside the US, a long-acting depot form treats infantile spasms, a severe epilepsy of babies; in a large analysis it stopped spasms about as often as high-dose prednisolone. The Cortrosyn label warns of hypersensitivity reactions and diagnostic inaccuracies, an audit found adverse events in about 6% of tests, and tetracosactide is named on WADA's Prohibited List.

Structured data

At a Glance

Every value in this table is printed from the Grey Peptides dataset, the same record the compound explorer and comparison tool read, so the three can never disagree.

ClassA synthetic peptide made of the first 24 amino acids of ACTH, which carries the hormone's full activity on the adrenal glands; FDA-approved since 1970 as Cortrosyn for testing adrenal function, and used outside the US as a depot injection for infantile spasms.
SequenceSYSMEHFRWGKPVGKKRRPVKVYP
Label dose0.25 mg (single dose for the stimulation test (0.125 mg from birth to under 2 years), intravenous or intramuscular)
US statusFDA Approved
Evidence levelHigh
Last reviewed2026-10-03

Educational information, not medical advice. The doses on this page come from approved labels, published studies and, where no study exists, amounts reported by users. None is a recommendation for you. An unapproved compound has no established safe or effective human dose, and products sold for “research use only” are not made or tested for people. Talk to a doctor before acting on anything on this site, including before you start, stop or change any medicine or dose. Full medical disclaimer.

Evidence

Published Research

The studies behind tetracosactide, read from their PubMed abstracts.

Human2023

Depot vs prednisolone for infantile spasms

Among 126 infants in a prospective analysis embedded in the ICISS trial, spasms had stopped on days 13 to 14 in 76% on tetracosactide depot and 67% on prednisolone, not a significant difference; development scores and later epilepsy rates also did not differ significantly.

PMID: 36621063
Human2024

How the short Synacthen test is used

Among 363 patients tested in Queensland public hospitals in 2020, the suspected cause of adrenal insufficiency was unclear in 46% of requests, morning cortisol was checked first in only 69%, more than one in six tests could have been avoided, and 6.1% had a documented adverse event.

PMID: 38660891
Human2022

Cosyntropin vs vigabatrin, randomised

In an underpowered trial of 34 children with new infantile spasms, spasms and the abnormal EEG resolved by day 14 in 75% on cosyntropin injectable suspension, 11% on vigabatrin and 38% on both. Adverse events occurred in 86% overall, with no difference between arms.

PMID: 35044272
Human2024

No benefit for post-dural puncture headache

In 234 deliveries complicated by accidental dural puncture, headache occurred in 60% of patients given prophylactic cosyntropin and 64% of those not given it, a difference that was not significant; epidural blood patch use also did not differ.

PMID: 39306572
Human2020

A nasal stimulation test

Nasal tetracosactide formulated with chitosan had a bioavailability of 14.3%, and 500 µg produced plasma cortisol at 60 minutes not significantly different from the standard 250 µg intravenous test; salivary cortisol and cortisone offered a needle-free measure, and children responded like adults.

PMID: 32593173
Human2023

Testing during haemodialysis

In 28 patients on chronic haemodialysis, cortisol concentrations 30 and 60 minutes after standard- and low-dose Synacthen were equivalent whether the test was done before or during dialysis, so the test can be run during a session; in 10 of 56 low-dose tests cortisol peaked by 20 minutes.

PMID: 37936106
Safety

Side Effects & Contraindications

Reported Side Effects

From the studies above.

● Adverse events in about 6% of short Synacthen tests in one hospital audit
● Serious reactions, most often infection, during hormonal treatment of infantile spasms

Contraindications & Cautions

Warnings from the Cortrosyn label (DailyMed, effective January 30, 2025).

● Hypersensitivity reactions
● Diagnostic inaccuracies: glucocorticoids, spironolactone and other factors can distort results
Questions

Frequently Asked Questions

?What is the cosyntropin test?

A blood test of adrenal function: cortisol is measured before an injection of cosyntropin and 30 and 60 minutes after. A weak rise suggests adrenal insufficiency.

?Is tetracosactide the same as ACTH?

It is the first 24 of ACTH's 39 amino acids, made synthetically, which carry the hormone's full activity on the adrenal glands.

?Is tetracosactide banned in sport?

Yes. WADA's Prohibited List names it under corticotrophins and their releasing factors.

Bibliography

References

  1. [fda] US FDA, Drugs@FDA (openFDA): CORTROSYN (cosyntropin), NDA 016750, original approval April 22, 1970, prescription; cosyntropin ANDA 202147. Read October 3, 2026.
  2. [fda-pi] FDA. Cortrosyn (cosyntropin) US prescribing information (DailyMed set 746856e9-3930-4f6a-b8e6-a03845d6dd0b, effective January 30, 2025). Read October 3, 2026.
  3. [clinical-trial] Osborne JP, et al. "Prednisolone or tetracosactide depot for infantile epileptic spasms syndrome? A prospective analysis of data embedded within two randomised controlled trials." Eur J Paediatr Neurol, 2023;42:110-116. PMID: 36621063.
  4. [pubmed] Wootton E, et al. "A retrospective review of the short Synacthen test in Queensland hospitals." Intern Med J, 2024;54(9):1515-1522. PMID: 38660891.
  5. [clinical-trial] Knupp KG, et al. "Comparison of Cosyntropin, Vigabatrin, and Combination Therapy in New-Onset Infantile Spasms in a Prospective Randomized Trial." J Child Neurol, 2022;37(3):186-193. PMID: 35044272.
  6. [pubmed] Ellis E, et al. "Prophylactic cosyntropin after unintentional dural puncture and incidence of post-dural puncture headache and epidural blood patch use: A retrospective cohort study (2019-2022)." Int J Obstet Anesth, 2024;60:104262. PMID: 39306572.
  7. [clinical-trial] Elder CJ, et al. "Pharmacodynamic studies of nasal tetracosactide with salivary glucocorticoids for a noninvasive Short Synacthen Test." J Clin Endocrinol Metab, 2020;105(8). PMID: 32593173.
  8. [clinical-trial] Nickler M, et al. "Performance of synacthen test in chronic hemodialysis patients." BMC Nephrol, 2023;24(1):330. PMID: 37936106.

Sources & Citations

Studies were read from their PubMed records; regulatory sources are listed below, read October 3, 2026.

Medical Disclaimer: This content is for educational and informational purposes only. It is not medical advice, and nothing here is an instruction to obtain or use any compound. Consult a licensed healthcare provider before making health decisions.

Last reviewed: 2026-10-03