NDASUBLINGUALTABLET
Approved
Nov 2018
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
20
Data completeness
5/8 — Partial
Drug Shortage Active
DSUVIA is currently in shortage. Reason: Available. This may impact manufacturing, supply chain, and quality hiring at the manufacturer.
DSUVIA (sufentanil) by Convert Pharmaceuticals is full opioid agonists [moa]. First approved in 2018.
Drug data last refreshed 3h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
DSUVIA (sufentanil) is a sublingual tablet formulation of sufentanil, a potent full opioid agonist approved in 2018 for acute pain management. It is indicated for rapid-onset, short-duration pain relief in opioid-tolerant patients in medically supervised settings. The drug works by binding to mu-opioid receptors in the central nervous system to produce analgesia.
Peak11.4 years to LOE
Product is at peak lifecycle stage with strong patent protection through 2038; commercial teams are focused on market penetration and maintaining market share against low competitive pressure.
Mechanism of Action
Full Opioid Agonists
Pharmacologic Class:
Opioid Agonist
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
DSUVIA Early Evaluation of Pain Trial
Started Aug 2022
150 enrolled
Traumatic Injury
Dexmedetomidine and Sufentanil Effect in PCA on Pediatric Patients Undergoing Scoliosis Surgery
Started Sep 2020
84 enrolled
Dexmedetomidine
Study to Evaluate the Overall Performance of the Zalviso System™ (Sufentanil Sublingual Tablet System) 15 mcg
Started Sep 2016
320 enrolled
Moderate-to-severe Acute Pain
A Multicenter, Open-Label Trial to Evaluate the Safety and Efficacy of the Sufentanil Sublingual Tablet 30 mcg in Patients With Post-Operative Pain
Started Mar 2016
140 enrolled
Acute Moderate-to-severe Pain
Open-Label Safety and Efficacy of the Sufentanil Sublingual Tablet 30 mcg for Acute Pain
Started Oct 2015
76 enrolled
Moderate-to-severe Acute Pain
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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.