साक्ष्य सामग्री अंग्रेजी में रखी जाती है।

Cosyntropin के लिए आदर्श संरचना चित्रण

अनुक्रम से निर्मित आदर्श अनुरूपक; कोई प्रायोगिक या पूर्वानुमानित संरचना नहीं.

एक नज़र में

ENTRY TYPE
approved drug
IDENTITY
Sequence verified

No structure asset recorded

TOP EVIDENCE
Grade A — Diagnostic test for adrenal insufficiency (SST)
MAJOR STATUS
Jurisdiction-specific — see status table
SPORT
Prohibited — as of 2026-08-06
VERIFIED
2026-08-06

Bottom line

Cosyntropin is a synthetic fragment of adrenocorticotropic hormone (ACTH 1-24) used as the reference standard diagnostic agent for the short ACTH stimulation test in suspected adrenal insufficiency. FDA approved as Cortrosyn (diagnostic use only). In some jurisdictions, Synacthen has limited therapeutic uses. It is the most widely accepted screening test for adrenal insufficiency.

Identity and composition

FieldVerified information
Preferred nameCosyntropin
Key aliasesCortrosyn (US), Synacthen (EU), tetracosactide, ACTH(1-24)
Molecular/sequence identitySer-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro (24 aa, N-terminal 24 residues of human ACTH)
Modifications/formAcetate salt; / injection ( powder, )
Stable identifiersUNII: 1693D3V8P0; : 16129617; CAS: 16960-16-0 (base); DrugBank: DB01284
Identity caveatsSynthetic fragment, not the full 39-aa ACTH. Inactive for melanocyte-stimulating effects (missing C-terminal 15 aa).

Development and approval status

JurisdictionStatus and indicationProduct/sourceAs of
US (FDA)Approved: diagnostic test for adrenocortical insufficiencyCortrosyn (Amphastar)1970s; NDA 017975
EU/EEA (EMA)Approved: diagnostic test; limited therapeutic use in infantile spasms (some countries)Synacthen (Novartis/Mallinckrodt)1970s
UK (MHRA)Approved: diagnostic test; therapeutic for infantile spasms (off-label in some settings)Synacthen
Status is multi-axis
Cosyntropin authorization and sport-status profileFour medicine-authorization axes reproduce only documented status rows; sport status is shown separately.UNITED STATESApproved: diagnostic test foradrenocortical insufficiencySOURCE / AS OFROW 1 / 1970s; NDA 017975EU/EEAApproved: diagnostic test;limited therapeutic use inSOURCE / AS OFROW 2 / 1970sUNITED KINGDOMApproved: diagnostic test;therapeutic for infantileSOURCE / AS OFROW 3 / —OTHER DOCUMENTEDSOURCE ROW OMITTEDSEE AUDIT REASONSOURCE / AS OFNOT PRESENT / NOT RECORDEDSPORT STATUS — SEPARATE FROM MEDICINE AUTHORIZATIONWADA: prohibited at all times under S2.2.2; tetracosactide (cosyntropin/ACTH 1-24) isexplicitly named. A TUE is an individual authorization and cannot be assumed from diagnostic
Authorization belongs to the named product, use, place, and date; sport status is independent.
पाठ विकल्प
UNITED STATES
US (FDA): Approved: diagnostic test for adrenocortical insufficiency
EU/EEA
EU/EEA (EMA): Approved: diagnostic test; limited therapeutic use in infantile spasms (some countries)
UNITED KINGDOM
UK (MHRA): Approved: diagnostic test; therapeutic for infantile spasms (off-label in some settings)
OTHER DOCUMENTED
No OTHER DOCUMENTED row is present in the source status table

Sport status: WADA: prohibited at all times under S2.2.2; tetracosactide (cosyntropin/ACTH 1-24) is explicitly named. A TUE is an individual authorization and cannot be assumed from diagnostic use. Glucocorticoids are regulated separately under S9.

Mechanism and pharmacology

ACTH receptor (MC2R) agonist. Binds to MC2R on the adrenal cortex, stimulating cortisol, aldosterone, and adrenal androgen synthesis and release. In the standard short synacthen test (SST), cosyntropin 250 mcg / produces maximal adrenal stimulation, with serum cortisol measured at 0 and 30–60 minutes.

Evidence by claim

Claim/indicationStageGradeBest human evidenceMain resultImportant limitations
Diagnostic test for adrenal insufficiency (SST)ApprovedAMultiple prospective cohort validation studies; reference standard250 mcg cosyntropin is the reference standard for diagnosing adrenal insufficiency30-min cortisol threshold varies (500–600 nmol/L); not validated in all critically ill populations
साक्ष्य ग्रेड
  • Aग्रेड A: विशिष्ट लेबल वाले उपयोग के लिए स्थापित
  • Bग्रेड B: मध्यम मानव साक्ष्य
  • Cग्रेड C: प्रारंभिक मानव साक्ष्य
  • Dग्रेड D: केवल प्रीक्लिनिकल
  • Eग्रेड E: उपाख्यानात्मक/विपणन दावा
  • Xग्रेड X: साक्ष्य दावे का खंडन करता है या समर्थन नहीं करता
साक्ष्य ग्रेडिंग के बारे में और जानें
Claim-evidence profile
Cosyntropin claim-evidence profileA: 1 claim; B: 0 claims; C: 0 claims; D: 0 claims; E: 0 claims; X: 0 claimsCONTRADICTORY / NON-SUPPORTIVEA — Established for a specific labeled useGrade A: Established for a specific labeled use — current approval plus adequate controlled trials and post-market context.1 claimDiagnostic test for adrenal insufficiency…B — Moderate human evidenceGrade B: Moderate human evidence — multiple controlled studies or a strong pivotal study, but no current approval for the claim.0 claimsC — Preliminary human evidenceGrade C: Preliminary human evidence — small, uncontrolled, surrogate-endpoint, or early-phase studies.0 claimsD — Preclinical onlyGrade D: Preclinical only — in vitro or animal evidence with no adequate human efficacy evidence.0 claimsE — Anecdotal/marketing claimGrade E: Anecdotal/marketing claim — testimonials, extrapolation, or vendor claims without adequate scientific support.0 claimsX — Evidence contradicts or does not support the claimGrade X: Evidence contradicts or does not support the claim — adequate negative evidence, failed program, or claim inconsistent with the studied material.0 claims
This counts the page's claim rows; it does not average them into a score.
पाठ विकल्प

Text alternative for the claim-evidence diagram. Each grade is defined below:

AEstablished for a specific labeled use
1 claim: Diagnostic test for adrenal insufficiency (SST)
BModerate human evidence
0 claims
CPreliminary human evidence
0 claims
DPreclinical only
0 claims
EAnecdotal/marketing claim
0 claims
XEvidence contradicts or does not support the claim
0 claims
United StatesApproved: diagnostic test for adrenocortical insufficiency
EU/EEAApproved: diagnostic test; limited therapeutic use in infantile spasms (some countries)
United KingdomApproved: diagnostic test; therapeutic for infantile spasms (off-label in some settings)

Key studies

StudyDesign/populationExposure studiedEndpoints and resultLimitations
SST validation (multiple cohorts)Prospective diagnostic accuracy studies, healthy controls and adrenal insufficiency patientsCosyntropin 250 mcg /Cortisol peak >500–600 nmol/L at 30/60 min distinguishes normal vs impaired adrenal functionThresholds differ by assay; less reliable in critical illness

Dose and administration evidence

Approved labeled regimen

The label summary below is product-, indication-, and jurisdiction-specific; consult the full current label and a licensed clinician/pharmacist.

Diagnostic use (US label): 0.25 mg (250 mcg) or , with cortisol sampling according to the labeled diagnostic protocol. Cortrosyn is supplied as a prescription product; preparation must follow the exact current product label and the testing institution's protocol.

Studied regimens (not recommendations)

  • Low-dose SST: 1 mcg IV (proposed for mild secondary insufficiency; not standard).

  • Depot Synacthen (EU): 0.5–1 mg IM, used in some longer stimulation protocols.

What is not established

  • No established or recommended human dose for therapeutic uses (unless specifically indicated for infantile spasms under local protocols).

Safety

Established label risks

  • Hypersensitivity: Rare anaphylaxis; contraindicated in known allergy to cosyntropin or ACTH.

  • Electrolyte: Transient fluid/electrolyte changes with high/ repeated doses (rare in diagnostic use).

  • Injection site: Pain, erythema.

Human-study signals

  • Diagnostic single dose very well tolerated; minimal AEs in large series.

Unknowns and product-quality risks

  • Research-grade synthetic ACTH(1-24) vials not equivalent to pharmaceutical cosyntropin.

  • No known risks from single diagnostic dose.

Interactions and special populations

  • Corticosteroid use may suppress response (false positive).

  • Estrogens may increase cortisol-binding globulin (elevated baseline).

  • Pregnancy: diagnostic use with caution.

Regulatory, compounding, and sport notes

Evidence gaps

  • Optimal cortisol threshold by modern immunoassay and mass spectrometry.

  • Validation of SST in specific populations (obesity, cirrhosis, critical illness).

  • Low-dose (1 mcg) SST remains controversial without consensus cutoff.

Search notes

  • Databases and registries: DailyMed, PubMed, FDA

  • Search terms: cosyntropin, Cortrosyn, Synacthen, tetracosactide, short synacthen test, adrenal insufficiency

  • Last searched: 2026-08-06

  • Inclusion emphasis: Regulatory labels, diagnostic accuracy studies, clinical guidelines

Sources

  1. Cortrosyn (cosyntropin) prescribing information. DailyMed. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=746856e9-3930-4f6a-b8e6-a03845d6dd0b

  2. PubChem. Cosyntropin. https://pubchem.ncbi.nlm.nih.gov/compound/16129617

  3. DrugBank. Cosyntropin. https://go.drugbank.com/drugs/DB01284

  4. Dickstein G, et al. Low-dose and standard-dose cosyntropin test. J Clin Endocrinol Metab. 1997;82(9):3108–13. PMID: 9284753.

  5. WADA. 2026 Prohibited List. https://www.wada-ama.org/en/resources/world-anti-doping-program/prohibited-list

विशेषज्ञों की राय

विशेषज्ञ क्या कहते हैं

टिप्पणियाँ व्यक्तिगत राय हैं, साक्ष्य समीक्षा का हिस्सा नहीं; समावेश का अर्थ समर्थन नहीं है।

इस यौगिक के लिए इस एटलस द्वारा स्वीकृत स्रोतों — सहकर्मी-समीक्षित साहित्य, विश्वविद्यालय, अस्पताल और चिकित्सा समाज संचार, नियामक, और नामांकित वैज्ञानिक पत्रकारिता — में कोई सत्यापित विशेषज्ञ टिप्पणी नहीं मिली।

टिप्पणी का अभाव यौगिक के बारे में किसी भी दिशा में साक्ष्य नहीं है।

विक्रेता, क्लिनिक और सोशल मीडिया के दावे नीति द्वारा बाहर रखे गए हैं और टिप्पणी के रूप में नहीं गिने जाते।

इस यौगिक के लिए इस एटलस के स्रोतों में कोई सत्यापित विशेषज्ञ वीडियो नहीं मिला।

वीडियो टिप्पणी का अभाव यौगिक के बारे में किसी भी दिशा में साक्ष्य नहीं है।

विक्रेता और सोशल मीडिया के वीडियो नीति द्वारा बाहर रखे गए हैं और नहीं गिने जाते।

प्रश्न

Is cosyntropin FDA-approved?

Yes. Cosyntropin (Cortrosyn) is FDA-approved as a diagnostic agent for adrenocortical insufficiency testing. It is also EMA-approved as Synacthen. It is a synthetic fragment of endogenous ACTH (ACTH 1-24) used as the reference standard for the short ACTH stimulation test. In some jurisdictions, Synacthen has limited therapeutic uses.

What evidence supports cosyntropin for adrenal insufficiency testing?

Cosyntropin given as a standard IV or IM amount is the reference standard for diagnosing adrenal insufficiency based on multiple prospective cohort validation studies. Serum cortisol is measured at 0 and 30-60 minutes, with a peak above a laboratory-specific threshold distinguishing normal from impaired function. Thresholds vary by assay and may be less reliable in critical illness.

Is cosyntropin the same as natural ACTH?

No. Cosyntropin is a synthetic fragment containing only the first 24 of the 39 amino acids of endogenous ACTH. It lacks the C-terminal 15 amino acids responsible for melanocyte-stimulating effects. The N-terminal 24 residues are sufficient for full adrenocortical stimulation, making it an effective diagnostic agent.

What are cosyntropin's main safety signals?

The diagnostic single use is very well tolerated with minimal adverse events in large series. Rare risks include hypersensitivity reactions (anaphylaxis) and contraindication in known allergy. Transient fluid or electrolyte changes may occur with high or repeated amounts but are rare in diagnostic use.

Is cosyntropin prohibited in sport?

Yes. Cosyntropin (tetracosactide or ACTH 1-24) is explicitly prohibited at all times under WADA S2.2.2. A therapeutic use exemption is an individual authorization and cannot be assumed from diagnostic use. Glucocorticoids are regulated separately under WADA S9.

Is research-grade cosyntropin equivalent to pharmaceutical cosyntropin?

No. The monograph explicitly states that research-grade synthetic ACTH(1-24) vials are not equivalent to pharmaceutical cosyntropin. Cortrosyn is FDA-approved for diagnostic testing, while Synacthen approvals and uses are jurisdiction-specific.

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