Niclosamide In Moderate COVID-19

NCT ID: NCT04436458

Last Updated: 2022-02-21

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-01-20
• Study Completion Date: 2022-01-20

Brief Summary

This is a Phase 2, multicentre, randomized, double blind, 2 arm placebo-controlled study in adults with moderate COVID-19 with gastrointestinal signs and symptoms.

Conditions

COVID

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Niclosamide

Continued SOC therapy together with Niclosamide tablets for 14 days

Group Type: EXPERIMENTAL

Niclosamide Oral Tablet

Intervention Type: DRUG

Continued SOC therapy together with niclosamide TID for 14 days

Placebo

Continued SOC therapy together with placebo tablets matching niclosamide

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Continued SOC therapy together with placebo tablets matching niclosamide for 14 days

Interventions

Niclosamide Oral Tablet

Continued SOC therapy together with niclosamide TID for 14 days

Intervention Type: DRUG

Placebo

Continued SOC therapy together with placebo tablets matching niclosamide for 14 days

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients hospitalized for treatment of COVID-19 with or without pneumonia, who are expected to remain in hospital at least seven days after the randomization and who accept continuing to be assessed for the study procedures (home or outpatient unit) up to 6 weeks in case of discharge.
• Patients who prior to developing COVID-19 usually have normal bowel habits defined as at least 3 stools per week and no more than 3 stools per day.
• SARS-CoV-2 infection confirmed by RT-PCR in rectal swab (or stool test) ≤2 days before randomization by local or central lab.
• Diarrhea defined as at least 3 watery stools in the last 24 hours prior to enrolment

Exclusion Criteria

• At the time of randomization patients requiring ICU admission or patients with severe respiratory insufficiency requiring mechanical ventilation or with rapid worsening of respiratory function leading to expectation for mechanical ventilation or ICU admission.
• Evidence of rapid clinical deterioration or existence of any life-threatening co-morbidity or any other medical condition which, in the opinion of the investigator, makes the patient unsuitable for inclusion.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Entero Therapeutics

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

FW-COV-002

Identifier Type: -

Identifier Source: org_study_id