NDAINJECTIONINJECTABLEPriority Review
Approved
Mar 1984
Lifecycle
LOE Approaching
Competitive Pressure
60/100
Clinical Trials
2
Data completeness
3/8 — Basic
Priority Review
Drug data last refreshed 18h ago · AI intelligence enriched 4d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
DDAVP (desmopressin acetate) is a synthetic vasopressin analogue administered via injection used to treat central diabetes insipidus, nocturnal enuresis, and hemophilia A. It works by replacing or mimicking endogenous antidiuretic hormone (ADH) to increase water reabsorption in the kidneys and promote clotting factor release.
LOE Approaching
Product approaching loss of exclusivity with moderate competitive pressure (60/100), indicating potential team consolidation and shift toward generic/biosimilar management strategies.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (2)
The Effect of Combined Systematized Behavioural Modification Education Program (SyBeMeP) With DDAVP in Patients With Nocturia
Started Apr 2012
124 enrolled
Nocturia
Desmopressin Acetate 0.2 mg Tablets, Fasting
Started Jul 2003
48 enrolled
Healthy
Career Relevance
Only 2 linked positions available for DDAVP, predominantly in HR and organizational development rather than commercial or medical roles, reflecting the product's mature stage and sponsor's operational focus. Career progression here involves supporting organizational initiatives and culture management rather than product-driven sales or medical affairs growth.
Initiative Application (Full time) (m/f/d)
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.