Desmopressin
Desmopressin is an FDA-approved selective V2 receptor agonist in the Vasopressin Receptor Agonist class. Two structural modifications to vasopressin — deamination at position 1 and substitution of D-arginine at position 8 — give desmopressin strong selectivity for the V2 receptor over V1a, so antidiuretic activity is retained while pressor activity is largely lost.
For research use only.
Key Facts
- CAS
- —
- Molecular Weight (MW)
- 1069.2 g/mol
- Half-life
- —
- FDA status
- Approved
- Evidence level
- FDA Approved
- Human dose established
- Yes
- Administration Route
- Oral · Subcutaneous · Intravenous · Intranasal
- Frequency
- One to three times daily by indication; single infusion for bleeding
- Last updated
- Nov 7, 2026
- Reviewed
- Nov 7, 2026
Research summary
Synthetic vasopressin analog approved for central diabetes insipidus, primary nocturnal enuresis, nocturia, and for raising factor VIII and von Willebrand factor in mild haemophilia A and type 1 von Willebrand disease.
Research evidence
- Regulatory review (FDA label)3 reviewed sources
- Controlled human trialsNone in reviewed sources
- Early or uncontrolled human studiesNone in reviewed sources
- Lab & animal studiesNone in reviewed sources
How it works
Each step shows whether the sources Peptide Library has reviewed include that kind of research. Counts are reviewed sources, not every study ever published. Reviews and programme summaries that describe human use are shown as "reported", not as trials, and registered trials without published results are listed but not counted. A higher step means research has progressed further; it does not mean a compound works better or is safer. Compounds whose evidence has not been reviewed yet show "Not reviewed" instead of a guess.
Peptide Library's Desmopressin profile summarises 5 cited studies listed in the Science section, the compound's regulatory status, and research-protocol parameters reported for it. It is a research reference, not medical advice.
Desmopressin dosage evidence
Desmopressin has FDA-approved human dosages that differ by form and use. DDAVP tablets for central diabetes insipidus start at 0.05 mg twice daily, with most patients in the label's trials using 0.1–0.8 mg a day in divided doses; for bedwetting in children aged 6 and over they start at 0.2 mg at bedtime. DDAVP injection is 2–4 mcg a day for diabetes insipidus, and 0.3 mcg/kg intravenously (up to 20 mcg) in hemophilia A and type 1 von Willebrand disease.
| Human dosing established | Yes |
|---|---|
| Route | Oral · Subcutaneous · Intravenous · Intranasal |
| Frequency | One to three times daily by indication; single infusion for bleeding |
| Duration studied | Continuous for diabetes insipidus; as needed for bleeding |
| Titration | Each dose is adjusted to urine output, sleep and serum sodium, under fluid restriction. |
| Evidence level | FDA Approved |
| Last reviewed | 2026-11-07 |
Research-reported dosing
Doses as studied, one row per regimen. Different trials used different regimens; they are listed separately rather than averaged.
| Study / context | Population | Dose | Route | Frequency | Duration | Outcome studied | Source |
|---|---|---|---|---|---|---|---|
| FDA label — DDAVP tablets, central diabetes insipidusFDA-approved label · FDA prescribing information | Adults and children with central diabetes insipidus | Start 0.05 mg twice daily; 0.1–0.8 mg a day for most patients in trials, adjusted within 0.1–1.2 mg a day | Oral | Two or three divided doses daily | Continuous | Antidiuresis | DDAVP (desmopressin acetate) tablets — FDA prescribing information, DailyMed |
| FDA label — DDAVP tablets, primary nocturnal enuresisFDA-approved label · FDA prescribing information | Children aged 6 and over with primary nocturnal enuresis | 0.2 mg at bedtime, titrated up to 0.6 mg | Oral | Once nightly | Per label | Management of primary nocturnal enuresis | DDAVP (desmopressin acetate) tablets — FDA prescribing information, DailyMed |
| FDA label — DDAVP injectionFDA-approved label · FDA prescribing information | Central diabetes insipidus; hemophilia A with factor VIII above 5%; type 1 von Willebrand disease | Diabetes insipidus: 2–4 mcg a day in one or two doses. Hemophilia A and von Willebrand disease: 0.3 mcg/kg, maximum 20 mcg | Subcutaneous or intravenous (diabetes insipidus); intravenous infusion (bleeding) | Daily (diabetes insipidus); per bleeding episode or procedure | — | Antidiuresis; maintained hemostasis | DDAVP (desmopressin acetate) injection — FDA prescribing information, DailyMed |
Where sources disagree
- Oral doses are in milligrams and injected doses in micrograms because very little of an oral dose is absorbed. Figures from one form do not transfer to another.
- The DDAVP injection label carries a boxed warning that desmopressin can cause hyponatremia. The labels require fluid restriction and serum sodium checks during treatment.
Sequence & molecular data
| Molecular formula | C46H64N14O12S2 |
|---|---|
| Molecular weight | 1069.2 g/mol |
| PubChem CID | 5311065 |
| FDA UNII | ENR1LLB0FP |
| ChEMBL | CHEMBL1429 |
| DrugBank | DB00035 |
Identifiers link to the public PubChem, FDA Substance Registration (UNII), ChEMBL and DrugBank records for the same entity.
Science
Mechanism of Action
Two structural modifications to vasopressin — deamination at position 1 and substitution of D-arginine at position 8 — give desmopressin strong selectivity for the V2 receptor over V1a, so antidiuretic activity is retained while pressor activity is largely lost. V2 stimulation promotes renal water reabsorption, and separately triggers release of von Willebrand factor and factor VIII from vascular endothelial storage sites.
Studies
- A systematic review and meta-analysis assessing the efficacy of Tuina for nocturnal enuresis in children
- Desmopressin as a hemostatic and blood sparing agent in bleeding disorders
- Effect of Desmopressin on Bleeding After Heart Surgeries: A Narrative Review
- Desmopressin acetate the first sublingual tablet to treat nocturia due to nocturnal polyuria
- Desmopressin (Nocdurna and Noctiva) for nocturnal polyuria
Research statistics
3,764 PubMed publications · 60.2% human clinical research · 103 registered trials
Counts of published research through 2026-11-01, not evidence that it works. Publications by year, study types and trials · How publications are counted
Regulatory & research status
Desmopressin is an FDA-approved product for specific labelled indications. Approval does not extend to the research contexts described on this page, and approved products are prescription medicines.
| FDA status | Approved |
|---|---|
| Research status | Approved product (see FDA status) |
| Availability | Prescription-Only |
| WADA (sport) | Unknown / Not Listed |
| Library classification | FDA-Approved |
How FDA approval, compounding and research-only status differ
Benefits
—
Desmopressin side effects
No side effects listed yet for this entry.
Storage & stability
This compound is not supplied as a powder to be mixed, so the freeze-dried powder and reconstitution handling described for research peptides does not apply. Storage conditions are product-specific: follow the label or packaging of the product itself.
Desmopressin: frequently asked questions
What is Desmopressin?
Synthetic vasopressin analog approved for central diabetes insipidus, primary nocturnal enuresis, nocturia, and for raising factor VIII and von Willebrand factor in mild haemophilia A and type 1 von Willebrand disease.
How does Desmopressin work?
Two structural modifications to vasopressin — deamination at position 1 and substitution of D-arginine at position 8 — give desmopressin strong selectivity for the V2 receptor over V1a, so antidiuretic activity is retained while pressor activity is largely lost. V2 stimulation promotes renal water reabsorption, and separately triggers release of von Willebrand factor and factor VIII from vascular endothelial storage sites.
Is Desmopressin FDA approved?
Yes. Desmopressin is approved by the FDA, and approved products are prescription medicines. Approval is always for specific indications studied in clinical trials, so an approved status does not mean the compound is approved for every use it is discussed for. Research-chemical material sold under the same name is not the approved product.
What peptides are similar to Desmopressin?
Compounds most often compared with Desmopressin include Vasopressin, Terlipressin, Angiotensin II and Cetrorelix. They are grouped by shared mechanism or research area rather than by equivalence, and their regulatory status and evidence base differ.
References
- A systematic review and meta-analysis assessing the efficacy of Tuina for nocturnal enuresis in children — Front Pharmacol, 2024External reference
- Desmopressin as a hemostatic and blood sparing agent in bleeding disorders — Eur J Haematol, 2023External reference
- Effect of Desmopressin on Bleeding After Heart Surgeries: A Narrative Review — Anesth Pain Med, 2023External reference
- Desmopressin acetate the first sublingual tablet to treat nocturia due to nocturnal polyuria — Expert Rev Clin Pharmacol, 2021External reference
- Desmopressin (Nocdurna and Noctiva) for nocturnal polyuria — Med Lett Drugs Ther, 2019External reference
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Compiled by Peptide Library Editorial · Reviewed Aug 30, 2026 · Updated Nov 7, 2026 · Version 2
This Desmopressin profile is compiled from published literature (5 cited studies linked above), public regulatory records and chemical registries. It describes what research reports; it is not medical advice, and nothing here is a dosing recommendation for humans. Peptide Library does not sell peptides. Editorial policy · How profiles are compiled · Report an error
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