Assessment of a Novel Fixed-dose Combination (FDC) Drug VR-AD-1005 for the Treatment of Acute Watery Diarrhea in Cholera

Hunazine Biotech

Status and phase

Completed

Phase 2

Conditions

Cholera

Treatments

Drug: Placebo

Drug: VR-AD-1005

Study type

Interventional

Funder types

Industry

Identifiers

NCT06193408

PR-23089

Details and patient eligibility

About

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

Enrollment

150 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Signed informed consent.
Adults, both genders aged 18-65 years.
Acute watery diarrhea (defined as passage of three or more liquid stools within the 24 hours before admission) with severe dehydration on arrival.
Detection of V. cholerae by rapid diagnostic assay (e.g. dark field microscopy).

Exclusion criteria

Known or suspected hypersensitivity to trial product(s) or related products.
Subjects with passage of bloody stools or muco-purulent stools.
Subjects with chronic diarrhea (>4 weeks of Diarrhea).
Clinically significant concomitant systemic disease (i.e. cardiovascular diseases including heart failure, acute kidney injury, sepsis or life-threatening malignant cancer).
Mental incapacity, unwillingness, or language barriers, precluding adequate understanding or cooperation.
History of receiving antimicrobial or antidiarrheal drugs within 6 hours prior to admission.
Positive urine pregnancy test for all female patients
Failure to obtain informed consent.
Failure to definitively diagnose cholera via culture or RT-PCR