Safety and Efficacy of Inhaled XW001 For Hospitalized COVID-19 Patients Requiring Oxygen Therapy

Phase 2

Withdrawn

• Conditions: COVID-19 Acute Respiratory Distress Syndrome
• Interventions: Drug: XW001; Drug: Placebo

• Registration Number: NCT05083117
• Lead Sponsor: Sciwind Biosciences APAC CO Pty. Ltd.

Brief Summary

This is a multiregional, randomized, double-blind, placebo-controlled Phase 2 study in patients with confirmed symptomatic COVID-19, designed to evaluate the safety, tolerability, efficacy, and PK of XW001 (IL-29 analog) inhalation solution. The purpose of this study is to evaluate whether treatment with XW001 reduces the likelihood of worsening disease in patients with severe COVID-19. Hospitalized patients on oxygen therapy by mask or nasal prongs (WHO-OSCI score 4) will be enrolled.

Detailed Description

Treatment arm patients will receive inhaled XW001 1 mg and placebo arm patients will receive volume-matching placebo 1 mL, once daily, using a commercially available nebulizer for up to 14 days. Treatment should be continued until discharge or progression to score 6 or higher but maximum up to 14 days. Dosing must be started within 48 hours of hospitalization. In addition, both the treatment groups will receive SoC.

The present study is a pilot in the development phase and comprising approximately 120 patients. An independent, external Data Monitoring Committee (DMC) will review all the preliminary clinical data available, including safety, tolerability, efficacy, and PK for the first 20 patients. The decision to recruit the subsequent 100 patients will solely depend on safety and tolerability.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2021-10-17
• Study First Submitted QC: 2021-10-17
• Study First Posted: 2021-10-19
• Study Start: 2021-10-30
• Primary Completion: 2022-03-10
• Study Completion: 2022-04-10
• Status Verified: 2023-08
• Last Update Submitted: 2023-08-17
• Last Update Posted: 2023-08-21

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

1. Male or nonpregnant or nonlactating female, aged 18 to 70 years at the time of consenting

2. Hospitalized due to infection with SARS-CoV-2 confirmed on validated local RT-PCR or other equivalent assays within 48 hours prior to screening and within 96 hours prior to randomization

3. Assessed to be hospitalized cases (rated at WHO-OSCI score 4 [on oxygen therapy by mask or nasal prongs]) within 24 hours prior to randomization

4. Admitted to hospital as clinically indicated for management of severe COVID-19 defined by the following criteria:

   • Positive RT-PCR test for SARS-CoV-2 or an equivalent test

   • Symptom suggestive of severe systemic illness with COVID-19, which could include any symptom of moderate illness or shortness of breath at rest, or respiratory distress

   • Clinical signs indicative of severe illness with COVID-19, being given oxygenation and meeting one of the following:

     • Respiratory rate ≥30 breaths per minute
     • Heart rate ≥125 beats per minute
     • Oxygen saturation (SpO2) <94% on room air at sea level
     • Arterial partial pressure of oxygen (PaO2)/fraction of inspired oxygen (FiO2) <300 mmHg or SpO2/FiO2 <315 mmHg
     • Lung infiltrates >50%

   • No criteria for critical severity

5. Female of childbearing potential must be postmenopausal for 1 year or longer, surgically sterile or having used a medically effective method of contraception for at least 3 months prior to hospitalization

6. Willing and able to provide a signed and dated or electronic informed consent for participation in this study.

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Exclusion Criteria

Patients will be excluded from the study if they satisfy any of the following criteria at the screening visit unless otherwise stated:

1. Having become symptomatic (fever, cough, and other likely symptoms) or positive on virologic test for more than 8 days prior to hospitalization
2. Diagnosed with SARS-CoV-2 confirmed more than 48 hours prior to hospitalization, otherwise reconfirmed positive on repeated RT-PCR (local laboratory) or other equivalent assays within 48 hours prior to randomization
3. Having been hospitalized for more than 48 hours, or showing a worsening medical condition within 48 hours after hospitalization in the opinion of the investigator
4. Known to have received any approved or investigational COVID-19 vaccines within 6 months prior to randomization. Vaccination records can be self-reported by the patient if there is no recorded history
5. Known to have received any approved or investigational therapeutic agents against SARS-CoV-2 including convalescent plasma, monoclonal antibodies, except for remdesivir, dexamethasone, or IL-6 inhibitors as a part of SoC
6. Having received any investigational medicinal products within 90 days of randomization
7. On noninvasive ventilation, eg, continuous positive airway pressure or bilevel positive airway pressure or high-flow oxygen therapy (at WHO-OSCI score 5)
8. Intubated, ventilated (invasively), on any advanced organ/life support (pressors, renal replacement therapy, ECMO), or remaining in the intensive care unit (at WHO-OSCI score 6 and 7)
9. Known to be hypersensitive or allergic to any natural or recombinant protein products
10. Inability to utilize nebulized drugs, or history of bronchospasm with inhaled medications
11. Patients with cardiac disease (New York Heart Association III/IV), liver cirrhosis (>5 x upper limit of normal [ULN]), on chemotherapy, dialysis patients with estimated glomerular filtration rate <30 mL/min/1.73m2, or have other debilitating condition or any other clinically significant medical condition or laboratory abnormality that, in the opinion of the investigator, would jeopardize the safety of the patient or non- COVID-19 irreversible underlying condition with projected fatal course within 6 months or with high-risk of mortality
12. Female patients are pregnant or lactating, or male or female patients have a childbearing plan within 30 days prior to randomization until 90 days after the last dosing.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
XW001	XW001	Treatment arm patients will receive inhaled XW001 1 mg, once daily, using a commercially available nebulizer (Aerogen Solo, Aerogen Ireland) for up to 14 days. Treatment should be continued until discharge or progression to score 6 or higher but maximum up to 14 days. Dosing must be started within 48 hours of hospitalization.
Placebo	Placebo	Placebo arm patients will receive volume-matching placebo 1 mL, once daily, using a commercially available nebulizer (Aerogen Solo, Aerogen Ireland) for up to 14 days. Treatment should be continued until discharge or progression to score 6 or higher but maximum up to 14 days. Dosing must be started within 48 hours of hospitalization.

Primary Outcome Measures

Name	Time	Method
Incidence of treatment-emergent adverse events (TEAEs)	35 days	Incidence of treatment-emergent adverse events (TEAEs), grade ≥3 TEAEs, SAEs, TEAEs leading to premature discontinuation of study treatment, TEAEs leading to study discontinuation, and TEAEs leading to deaths
Change from the baseline in clinical laboratory results	35 days	Percentage of the lab results change
Incidence of clinically significant laboratory findings	35 days	Percentage of the lab results change
Change from the baseline in vital signs results	35 days	Vital signs will be recorded twice daily while the patient is hospitalized. Vital signs may also be performed at other times if judged clinically appropriate or if the ongoing review of the data suggests a more detailed assessment of vital signs is required.
Change from the baseline in electrocardiogram (ECG) findings	35 days	A 12-lead ECG is to be performed at screening in the supine position and at rest for at least 5 minutes. Additionally, a 12-lead ECG will be performed if QT abnormality is noted or early termination while the patient is hospitalized or at the discretion of the investigator.

Secondary Outcome Measures

Name	Time	Method
Time to clinical improvement from the time of randomization.	28 days	Time to clinical improvement is defined as the time (in days) from the randomization date to the first day on which a patient satisfies a score of 0, 1, 2, or 3 on the 9-point WHO-OSCI and maintains a score ≤3 at least 48 hours (initial improvement) and maintains this up to the 28-day timeframe (sustained improvement)
Time to hospital discharge from the time of randomization	28 days	At or below WHO-OSCI score 2 from the time of randomization
Time to clinical recovery from the time of randomization	28 days	Time of clinical recovery (in days) will be calculated using the WHO-OSCI from the randomization date to the first day on which the patient satisfies a score of 0 or 1 on the 9-point WHO-OSCI and remains at 0 or 1 until Day 28 (has no subsequent readmission for COVID-19 signs or symptoms)
Time to viral clearance	28 days	targeted not detected on real-time quantitative polymerase chain reaction \[qPCR\] assay) from the time of randomization
Viral load kinetics on real-time qPCR assay	28 days	A real-time qPCR will be done to determine the viral load kinetics in positive RT-PCR samples.
Proportions of patients experiencing clinical improvement, hospital discharge, clinical recovery, and viral clearance	28 days	The proportions of patients will be compared using the logistic regression.
Proportion of patients experiencing clinical progression from the time of randomization	35 days	The proportions of patients will be compared using the logistic regression.
Proportion of patients progressing to on noninvasive ventilation or high-flow oxygen from the time of randomization	35 days	The proportions of patients will be compared using the logistic regression.
Proportion of patients progressing to on intubation with ventilation from the time of randomization	35 days	The proportions of patients will be compared using the logistic regression.
Proportion of patients progressing to death from the time of randomization	35 days	Proportion of patients progressing to death (WHO-OSCI score 8) within the 35-day timeframe from the time of randomization
Changes from the baseline in the BCSS total score and breathlessness and cough subscores	35 days	Change from the baseline in the BCSS scores will also be evaluated daily. A physical examination including height and weight will be measured. Height will be measured at screening only. If a patient is not able to stand easily, the patient may provide height.
Changes from the baseline in the NEWS2	35 days	Change from the baseline in the NEWS2 scores will also be evaluated daily. A physical examination including height and weight will be measured. Height will be measured at screening only. If a patient is not able to stand easily, the patient may provide height.

Trial Locations

Locations (2)

Hospital Pirovano; 🇦🇷 Caba, Bs AS, Argentina

Hospital Nacional Arzobispo Loayza; 🇵🇪 Lima, Peru