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ECC4703 Food Effect and Relative Bioavailability Study in Healthy Adult Participants

StatusRecruiting
PhasePhase 1
SponsorEccogene
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 10 months later May 2026 → Apr 2027
See other at-risk trials from Eccogene

Record History

  1. Primary and study completion pushed from May 2026 to Apr 2027 Start date changed from estimate of Jan 10, 2026 to Jan 7, 2026v3 Show 1 more changeShow less
    • Start date changed from estimate of Jan 10, 2026 to Jan 7, 2026
  2. Trial status: Not Yet Recruiting to Recruiting Primary endpoints revised (10) · Study sites: 0 to 1 · Start date: Jan 2026 to Jan 10, 2026 · 1 morev2 Show 4 more changesShow less
    • Primary endpoints revised (10)
    • Study sites: 0 to 1
    • Start date: Jan 2026 to Jan 10, 2026
    • Study title expanded, about 3 words

    See this version in full on ClinicalTrials.gov ↗

  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Eccogene
4 trials monitored
See 2 trials at risk
NASH / MASH
654 trials monitored
See 22 trials at risk
This is a Phase I, open-label, randomized, single-dose, 2-part study designed to evaluate the food effect and relative bioavailability of ECC4703 in healthy adult participants.
Trial Details
NCT Number NCT07334080
Lead Sponsor Eccogene
Conditions Metabolic Dysfunction-Associated Steatohepatitis
Enrollment 72 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov