TrialSignal
Clinical trial intelligence report
An Open-Label, Phase 2, Long-Term Safety Study of Inhaled Insulin: An Up to Four-Year Extension of Therapy in Subjects With Type 1 or Type 2 Diabetes Mellitus Participating in Extension Protocols 217-102, 103, or 104
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT00143247-Jun 24, 2026
NCT ID
NCT00143247
Status
TERMINATED
Phase
Phase 2
Sponsor
Pfizer
Executive brief
Investment-Ready Snapshot
Pfizer's Exubera® was intended to provide a novel inhaled insulin delivery method for diabetes management. However, the product was withdrawn from the market due to poor commercial performance rather than safety concerns. The termination of this long-term safety study indicates a strategic pivot away from inhaled insulin therapies, suggesting limited future market potential for similar products. Competitors in the diabetes space may capitalize on this gap, focusing on alternative delivery methods or formulations. Diligence should consider the evolving landscape of diabetes management and the potential for inhaled therapies to regain interest with advancements in formulation technology.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00143247
Indication
Diabetes Mellitus
Modality
small molecule
Target
Inhaled insulin (Exubera®) for the treatment of Type 1 and Type 2 Diabetes Mellitus.
Intervention
Exubera® (inhaled insulin)
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.