NDAINTRAVENOUSPOWDERPriority Review
Approved
Jul 1976
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
1
Data completeness
4/8 — Partial
Priority Review
KINEVAC (sincalide) by Bracco. Approved for cholecystokinin analog [epc]. First approved in 1976.
Drug data last refreshed 9h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
KINEVAC (sincalide) is an intravenous cholecystokinin (CCK) analog approved in 1976 for diagnostic imaging of the biliary system. It stimulates gallbladder contraction and pancreatic secretion, enabling visualization during hepatobiliary scintigraphy. The drug is used to assess gallbladder function and detect biliary dyskinesia.
LOE Approaching
Late-lifecycle diagnostic agent with declining market relevance; teams are likely consolidating and focused on cost management rather than growth initiatives.
Mechanism of Action
Pharmacologic Class:
Cholecystokinin Analog
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (1)
Dose Response of Intravenous Sincalide(CCK-8) for Gallbladder Emptying
Started May 2008
60 enrolled
Healthy
Career Relevance
Working on KINEVAC offers limited career growth opportunities due to its LOE-approaching status and lack of active clinical development. Roles are primarily defensive and focused on margin protection and market maintenance rather than innovation and expansion.
Product Manager
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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.