TrialSignal
Clinical trial intelligence report
Safety, Reactogenicity, Tolerability, Immunogenicity and Efficacy of Live Attenuated ETEC ACE527 Vaccine Administered Alone or With a Double Mutant E. Coli Heat Labile Toxin (dmLT) in Healthy Adult Volunteers
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT01739231-Jul 28, 2026
NCT ID
NCT01739231
Status
COMPLETED
Phase
PHASE1
Sponsor
PATH
Executive brief
Investment-Ready Snapshot
Safety, Reactogenicity, Tolerability, Immunogenicity and Efficacy of Live Attenuated ETEC ACE527 Vaccine Administered Alone or With a Double Mutant E. Coli Heat Labile Toxin (dmLT) in Healthy Adult Volunteers is a PHASE1 clinical asset sponsored by PATH in Diarrhea. SEO and diligence focus: ACE527, dmLT, CeraVacx placebo, H10407 challenge strain, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01739231
Indication
Diarrhea
Modality
protein therapy
Target
ACE527, dmLT, CeraVacx placebo, H10407 challenge strain
Intervention
ACE527, dmLT, CeraVacx placebo, H10407 challenge strain
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.