TrialSignal
Clinical trial intelligence report
Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel-Groups, To Evaluate And Compare The Safety, Tolerability And Efficacy Of Two Dosages Of Inhaled TPI ASM8 Administered For 14 Days In Patients With Mild to Moderate Asthma.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT00402948-Jul 28, 2026
NCT ID
NCT00402948
Status
TERMINATED
Phase
Phase 2
Sponsor
Syntara
Executive brief
Investment-Ready Snapshot
Syntara's TPI ASM8 is positioned within the competitive landscape of asthma treatments, specifically targeting patients with mild to moderate asthma characterized by eosinophilic inflammation. The market for asthma therapeutics is substantial, with a growing demand for innovative inhaled therapies that offer improved efficacy and safety profiles. However, the trial was terminated due to lack of substantial enrollment, which raises concerns regarding market viability and the potential for future investment. The failure to recruit sufficient participants may indicate challenges in patient identification or interest, necessitating a reevaluation of the target population or recruitment strategies. This could impact Syntara's strategic planning and resource allocation moving forward.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00402948
Indication
Asthma
Modality
small molecule
Target
Inhaled TPI ASM8 targeting eosinophilic inflammation in asthma.
Intervention
TPI ASM8, ASM8
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.