Phase 3
N=49
Study of Niclosamide in Moderate and Severe Hospitalized Coronavirus-19 (COVID-19) Patients
COVID-19
Bottom Line
View on ClinicalTrials.gov: NCT04603924 ↗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
| Outcome | Result | p-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.
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.