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Clinical trial intelligence report
A Randomized, Blinded, Placebo Controlled, Safety and Pharmacodynamic Study of BHT-3021 With Open Label Cross-Over in Subjects With Type I Diabetes Mellitus
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT00453375-Jun 24, 2026
NCT ID
NCT00453375
Status
COMPLETED
Phase
Phase 1
Sponsor
Bayhill Therapeutics
Executive brief
Investment-Ready Snapshot
Bayhill Therapeutics is advancing BHT-3021 as a potential therapeutic option for Type 1 Diabetes Mellitus, a market characterized by significant unmet needs and a growing patient population. The asset's focus on immune modulation could position it favorably against existing therapies, particularly if safety and efficacy are demonstrated. The competitive landscape includes established players and emerging biopharma companies targeting similar pathways, necessitating thorough diligence on clinical outcomes and market entry strategies. The trial's completion in 2011 suggests that further development may hinge on subsequent studies or partnerships to leverage the data generated.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00453375
Indication
Diabetes
Modality
small molecule
Target
BHT-3021 targets autoimmune responses in Type 1 Diabetes Mellitus by modulating T cell responses to autoantigens such as insulin, GAD-65, and IA-2.
Intervention
BHT-3021, BHT-Placebo
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.