NDAINHALATIONGAS
Approved
Aug 2013
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
4/8 — Partial
MEDICAL AIR, USP (air) by Connect Biopharma. Approved for asthma, chronic obstructive pulmonary disease. First approved in 2013.
Drug data last refreshed 21h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
MEDICAL AIR, USP is a pharmaceutical-grade gaseous product approved for inhalation in asthma and chronic obstructive pulmonary disease (COPD). The product operates through simple respiratory gas delivery with no active pharmacological mechanism of action. It represents a commodity-like therapeutic category in respiratory care.
Peak
Product is at peak lifecycle but faces significant commoditization pressure; team growth opportunities are limited given low competitive differentiation and lack of active pharmacology.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications (2)
Clinical Trials (20)
Tapestry Rotator Cuff Repair PMCF
Started Dec 2026
170 enrolled
Rotator Cuff TearsRotator Cuff Injuries
Pharmacokinetics Study of Larotinib in Subjects With Impaired Hepatic Function
Started Oct 2026
32 enrolled
Esophageal CancerAdvanced Solid Tumor
Decellularized Human Placental Extracellular Matrix Tissue for Rotator Cuff Repair Augmentation
Started Aug 2026
120 enrolled
Rotator Cuff Tear
Study of Protection And Repair of Endothelial-glycocalyx in Sepsis (SPARES)
Started Jul 2026
45 enrolled
Sepsis
Mitral Valve Repair With the Chord-X System: A Long Term Evaluation
Started Jun 2026
110 enrolled
Mitral Regurgitation (MR)
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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.