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Phase 3 N=49 Randomized Quadruple-blind Treatment

Study of Niclosamide in Moderate and Severe Hospitalized Coronavirus-19 (COVID-19) Patients

COVID-19

Enrolled (actual)
49
Serious AEs
20.0%
Results posted
May 2025
Primary outcome: Primary: Number of Subjects Experiencing TEAEs — 16; 12; 9; 2 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Niclosamide (Drug); Placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
NeuroBo Pharmaceuticals Inc.
Primary completion
Feb 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Subjects Experiencing TEAEs
16; 12; 9; 2; 5; 4
PRIMARY
Number of Subjects Experiencing TESAEs
3; 6
SECONDARY
Median Time to Hospital Discharge
6.03; 13.92
SECONDARY
Median Time to 2-point Improvement WHO Clinical Improvement Scale
4.15; 13.91
SECONDARY
Median Time to Resolution of COVID-19 Symptoms
17; 16
SECONDARY
Median Time to Time-to-Viral Load Undetectable
13.09; 13.1
SECONDARY
AUC 0-t (h*ng/mL)
1728.6; 2839.0
SECONDARY
Cmax (ng/mL)
348.06; 435.91
SECONDARY
Tmax (h)
4.884; 3.983

Summary

Study of ANA001 in Moderate and Severe COVID-19 Patients

Eligibility Criteria

Key Inclusion Criteria

  • Provide written informed consent prior to performing study procedures
  • Hospitalized.
  • Male or female ≥18 years of age
  • Positive for severe acute respiratory syndrome coronavirus 2
  • Presence of symptoms of lower respiratory tract infection (LRTI) including at least 1 of the following: fever, cough, sore throat, malaise, headache, muscle pain, or more significant lower respiratory tract symptoms, including shortness of breath
  • At least 1 of the following: respiratory rate (RR) ≥20 breaths per minute, room air oxygen saturation (SpO2) 38.3°C
  • Women of childbearing potential must agree to abstinent or use at least 1 form of contraception not including hormonal contraception from the day of screening through Day 30

Key Exclusion Criteria

  • Hospitalized but no longer requires ongoing inpatient care (i.e., discharge is anticipated in ≤24 hours)
  • Patient is not anticipated to survive >48 hours OR is under palliative care
  • Evidence of critical illness, defined by at least 1 of the following:
  • Respiratory failure requiring at least 1 of the following:
  • Endotracheal intubation and mechanical ventilation, oxygen delivered by high flow nasal cannula
  • Noninvasive positive pressure ventilation (NIPVV), OR
  • Extracorporeal membrane oxygenation (ECMO) or clinical diagnosis of respiratory failure
  • Shock (defined by systolic blood pressure (BP) <90 mm Hg, or diastolic blood pressure (BP) <60 mm Hg or requiring vasopressors), OR
  • Multi-organ dysfunction/failure
  • Severe central nervous system (CNS) conditions
  • Chronic kidney disease requiring dialysis
  • Known allergy to the study drug or salicylate containing medications.
  • Suspected and/or confirmed pregnancy or breastfeeding
  • Current or planned participation in any other clinical trial of a treatment being developed under a US investigational new drug (IND) or emergency use authorization (EUA).
  • Patients receiving chemotherapeutic agents and/or immunomodulators (including monoclonal antibodies (Mabs) or plasma transfusions) for chronic disease conditions.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04603924). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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