NDAINHALATIONGAS
Approved
Mar 1982
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
14
Data completeness
4/8 — Partial
XENON XE 133 (xenon) by Curium Pharma is radiopharmaceutical activity [moa]. First approved in 1982.
Drug data last refreshed Yesterday
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Xenon XE-133 is a radiopharmaceutical inhalation diagnostic agent used to detect pulmonary embolism and assess regional lung ventilation in chronic obstructive pulmonary disease. It works through radiopharmaceutical activity, allowing visualization of gas distribution in the lungs via imaging. The product is administered as an inhaled gas and approved since 1982.
LOE Approaching
This legacy diagnostic product faces moderate competitive pressure (30/100) with no recent market growth data; expect smaller commercial teams focused on maintenance rather than expansion.
Mechanism of Action
Radiopharmaceutical Activity
Pharmacologic Class:
Inhalation Diagnostic Agent
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (14)
129 Xenon Imaging in Patients Treated With Sotatercept
Started Oct 2025
14 enrolled
Pulmonary HypertensionPulmonary Arterial Hypertension
Hyperpolarized Xenon Functional Lung Imaging in COPD Patients Undergoing Targeted Lung Denervation
Started Sep 2025
0COPD
Xenon MRI in Stable Pulmonary Hypertension (Jupiter AUGEAN)
Started Mar 2024
0Pulmonary Artery Hypertension
Xenon MRI and Progressive ILD
Started Jul 2022
60 enrolled
Idiopathic Pulmonary FibrosisProgressive Pulmonary Fibrosis
Evaluating the Effect of Benralizumab in Severe, Poorly-controlled Eosinophilic Asthma Using Inhaled Hyperpolarized 129-Xenon MRI
Started Mar 2022
29 enrolled
Asthma; Eosinophilic
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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.