CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 150 enrolled / 150 target
Drug / intervention
VR-AD-1005 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06193408
NCT06193408Phase 2CompletedHigh Momentum (5.2/mo)Completion was 22mo ago

Assessment of a Novel Fixed-dose Combination (FDC) Drug VR-AD-1005 for the Treatment of Acute Watery Diarrhea in Cholera: a Phase II, Randomized, Placebo-controlled, Double-blinded Efficacy and Safety Trial

Hunazine Biotech S.L.·interventional·Posted Jan 5, 2024·Updated Jun 2, 2026

In Brief

A Phase 2 clinical trial evaluating VR-AD-1005 and Placebo for Cholera. Completed, enrolled 150 participants across 1 site.

Signals

Enrolling ahead of pace

Detailed Summary

Cholera still remains a global public health concern affecting both children and adults, and patients can succumb in quick time if remain untreated. Cholera is a secretory diarrhea and is generally treated with oral or intravenous rehydration therapy to compensate for the fluid loss. However, antimicrobial treatment is given to patients with moderate to severe diarrhea. The consistent emergence of multidrug-resistant bacteria is a major concern for the management of infectious diseases including cholera. No antisecretory drug has so far been proven successful. In a phase II clinical trial, the investigators will assess the effectiveness of a novel antisecretory drug VR-AD-1005 for treating cholera. Changes in stool volume and rehydration therapy will be assessed for VR-AD-1005 in comparison with placebo. If successful, this will be a huge advance in managing cholera and other secretory diarrhea. The introduction of the antisecretory drug can minimize the hospital stay and reduce antibiotic use, which in turn can reduce the emergence of antibiotic resistance among pathogens

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCholera
CountriesBangladesh
Collaborators--

Timeline

Phase 2CompletedFinished
202420252026
First PostedJan 5, 2024
Enrollment StartFeb 11, 2024
Primary CompletionAug 11, 2024
Study CompletionSep 8, 2024
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 2.5 years ago

Arms & Interventions

VR-AD-1005experimental

Drug: VR-AD-1005
Placeboplacebo_comparator

Drug: Placebo

Interventions

VR-AD-1005drug

oral capsule

Placebodrug

oral capsule