NCT04365868Phase 2, phase 3Terminated

Study Evaluating the Efficacy and Safety of Belapectin for the Prevention of Esophageal Varices in NASH Cirrhosis

Study sponsor: Galectin Therapeutics Inc. · GALT

Compare the available registry edits below. Primary completion is the date data collection ends for the main study measures; it does not tell you when results will be published.

Primary completion2025-03-11Actual
Enrollment · participants357Actual
Source updated2026-06-30Last update listed in the registry record
Version history

Changes to this trial

Last 12 months
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· 1 field changed

Main study measure wording changed

Text changed; whether the study measures changed has not been verified. Saved text may be shortened.

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− Before

Measure: Proportion of patients in the belapectin treatment groups who develop new esophageal varices at 78 weeks [18 months] of treatment compared to placebo

+ After

Measure: Proportion of Patients in the Belapectin Treatment Groups Who Develop New Esophageal Varices at 78 Weeks [18 Months] of Treatment Compared to Placebo

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· 1 field changed

Recruitment status changed

− Before

Active not recruiting

+ After

Terminated

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