Silmitasertib (CX-4945) in Patients With Severe Coronavirus Disease 2019 (COVID-19)

Phase 2

Terminated

• Conditions: Coronavirus
• Interventions: Drug: Silmitasertib

• Registration Number: NCT04668209
• Lead Sponsor: University of Arizona

Brief Summary

This multi-center, open-label, 2 arm parallel-group, randomized, interventional prospective exploratory study in 40 patients aimed to evaluate safety and explore putative clinical benefits of Silmitasertib 1000 mg BID dose in patients with severe illness caused be SARS-COV-2. This will be a two-arm trial comparing the SOC/best supportive care alone to the SOC/best supportive care with addition of Silmitasertib (allocation ratio 1:1).

Detailed Description

This is a phase II multi-center, randomized, open-label, 2 arm parallel-group controlled interventional prospective study of CX-4945 in patients with severe COVID-19. Up to approximately 40 patients will be enrolled into this study. A screening evaluation will occur within 7 days prior to Day 1. All qualified patients will be randomized at Day 1 in a ratio of 1:1 to one of the following two treatment arms:

Arm A: SOC/ best supportive care in combination with CX-4945 1000 mg BID PO or Arm B: SOC/ best supportive care alone The standard of care (SOC) is not pre-specified, may vary among patients, and may include agents with anti-viral activity, such as remdesivir, among others. Investigator discretion is to be applied for any established SOC. Active concomitant treatment with other investigational antivirals or immunomodulators are not permitted Best supportive care is defined as intensive care therapy according to current guidelines, evidence, and best practice, including but not limited to lung protective ventilation, thrombosis prophylaxis, renal replacement therapy when indicated, and access to advanced therapies including extracorporeal membrane oxygenation.

The total duration of the treatment will be 14 days. Patients will be followed up at 28, 45 and 60 days from the start of the treatment. The total duration for each patient in the study (including the screening) will be up to 67 days.

Study Timeline

• Study First Submitted: 2020-12-02
• Study First Submitted QC: 2020-12-11
• Study First Posted: 2020-12-16
• Study Start: 2021-01-21
• Primary Completion: 2022-06-30
• Study Completion: 2022-10-19
• Status Verified: 2022-11
• Results First Submitted: 2023-06-09
• Results First Submitted QC: 2023-07-21
• Results First Posted: 2023-08-14
• Last Update Submitted: 2023-10-16
• Last Update Posted: 2023-11-07

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 31

Inclusion Criteria

1. Male or non-pregnant female adult ≥ 18 years of age

2. Diagnosed/confirmed with COVID-19 by standard RT-PCR assay or equivalent testing within 7 days prior to randomization (Day1).

3. Hospitalized patient with severe illness caused by SARS-CoV-2 (Note: Prior or current use of remdesivir or dexamethasone (SOC) are allowed under the investigator's discretion. Concomitant treatment with other investigational antiviral drugs or immunomodulators are not permitted from Day1 through Day 28)

   Symptoms of severe systemic illness/infection with COVID-19:

   At least 1 of the following: fever, cough, sore throat, malaise, headache, muscle pain, shortness of breath at rest or with exertion, confusion, or symptoms of severe lower respiratory infection including dyspnea at rest or respiratory distress AND Clinical signs indicative of severe systemic illness/infection with COVID-19 At least 1 of the following: RR ≥ 30, HR ≥ 125, SaO2 <93% on room air or requires > 2L oxygen by nasal cannula in order to maintain SaO2 ≥93%

4. Patient (or legally authorized representative) provides written informed consent prior to initiation of any study procedures.

5. Adequate hematopoietic capacity, as defined by the following:

   1. Hemoglobin ≥ 9.0 g/dL and not transfusion dependent
   2. Platelets ≥ 100,000/mm3
   3. Absolute neutrophil count ≥ 1500 cells/mm3

6. Adequate hepatic function, as defined by the following:

   1. AST and ALT ≤ 2.5 times upper limit of normal (ULN)
   2. Total bilirubin ≤ 1.5 x ULN
   3. Albumin ≥ 3.0 g/dL

7. Adequate renal function, as defined by the following:

   a. Renal: calculated creatinine clearance >45 mL/min for patients with abnormal, increased creatinine levels (Cockcroft-Gault formula).

8. Ability to take oral medication and be willing to adhere to drug administration and premedication requirements (see Section 6.3) throughout study duration.

Exclusion Criteria

1. Patient showing signs of respiratory failure necessitating mechanical ventilation
2. Pregnant or nursing women. NOTE: Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence) prior to study entry and for the duration of study participation. Should a man father a child, or a woman become pregnant or suspect she is pregnant while participating in this study, he or she should inform the treating physician immediately.
3. Active or uncontrolled infections other than COVID-19 or with serious illnesses or medical conditions which would not permit the patient to receive study treatment
4. Active or planned concomitant treatment with other investigational antivirals or immunomodulators
5. Chronic diarrhea (excess of 2-3 stools/day above normal frequency)
6. Current use or anticipated need for drugs that are known strong inhibitors or inducers of major CYP enzymes.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Silmitasertib	Silmitasertib	Standard of care / supportive care in combination with Silmitasertib (CX-4945)

Primary Outcome Measures

Name	Time	Method
Incidence of Treatment Emergent Adverse Events [Safety and Tolerability]	Through Day 60	Adverse Events experienced by the patients from randomization to Day 60 (including vital signs, physical findings, clinical laboratory, and ECG results) as characterized by type, frequency, severity (as graded by Common Terminology Criteria for Adverse Events (CTCAE version 5.0), timing, seriousness, and relationship to study therapy.

Secondary Outcome Measures

Name	Time	Method
To Evaluate Changes in CPK	Assessed on Days 1, 4, 8, 11, and 14	CPK level
To Evaluate Changes in Ferritin	Assessed on Days 1, 4, 8, 11, and 14	Ferritin level
To Evaluate Changes in D-dimer	Assessed on Days 1, 4, 8, 11, and 14	D-dimer level
To Evaluate Changes in LDH	Assessed on Days 1, 4, 8, 11, and 14	LDH level
To Evaluate Preliminary Evidence of Anti-viral Activity of CX-4945 as Compared to the Control Arm.	Through Day 14	Changes in chest imaging from Screening to Day 5 or 14
Number of Days Hospitalized	Through Day 28	Days of hospitalization from randomization through Day 28
To Evaluate Changes in IL-6 Level	Assessed on Days 1, 4, 8, 11, and 14	IL-6 level
To Evaluate Changes in CRP	Assessed on Days 1, 4, 8, 11, and 14	CRP level
To Compare Time to Clinical Recovery in CX-4945 Treatment Group Evaluated From Randomization Through Day 28 as Compared to the Control Arm.	Through Day 28	Number of days from randomization to the first day on which the subject satisfies one of the following three categories from the ordinal NIAID 8- point Clinical Progression Outcomes scale collected daily from randomization through Day 28: Hospitalized, not requiring supplemental oxygen - no longer requires ongoing medical care; Not hospitalized, limitation on activities and/or requiring home oxygen; Not hospitalized, no limitations on activities.
To Compare Changes in Clinical Status of Patients Enrolled to CX-4945 Treatment Arm as Compared to the Control Arm at Day 14 and Day 28.	Through Day 28	Percentage of Participants at Each Clinical Status at Day 14 and Day 28 assessed by using the ordinal NIAID 8- point Clinical Progression Outcomes scale (Scale ranges from 1 (Death) to 8 (Not hospitalized, no limitations on activities)
Number of Days of Supplemental Oxygen Use	Through Day 28	Days of supplemental oxygen (if applicable) from randomization through day 28
All-cause Mortality Status	Through Day 60	The number of deaths occurred in each treatment group from randomization through Day 60
Number of Days of On-invasive Ventilation/High Flow Oxygen	Through Day 28	Days of non-invasive ventilation/high flow oxygen (if applicable) from randomization through day 28
Number of Days of Invasive Mechanical Ventilation/ECMO	Through Day 28	Days of invasive mechanical ventilation/ECMO (if applicable) from randomization through Day 28.
Number of Patients Returned to Room Air	Through Day 28	Number of patients returned to room air after randomization through Day 14 or Day 28.
Change in Pulse Oxygen Saturation	Days 4, 8, 11, 14, and 28	Change in pulse oxygen saturation (SpO2) from randomization to Day 4, 8, 11, 14 and 28
Number of Thrombosis Events	Through Day 28	Number of documented venous thromboembolism (VTE), arterial thrombosis (stroke, myocardial infarction, other) and microthrombosis events from randomization through Day 28
Changes in EQ-D5-5L	Days randomization, 8, 14 and 28	The EuroQol 5 Dimension 5 Level (EQ-5D-5L) is a self-report survey that measures quality of life across 5 domains: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension is scored on a 5-level severity ranking that ranges from no problems (Level 1); slight; moderate; severe; and extreme problems (Level 5). Higher values indicate worse outcomes, while lower indicate better outcomes. The subscales are combined to compute a total score and averaged to produce the mean and SD.; Changes in EQ-D5-5L (used as an indicator of symptom improvement) from randomization to Day 8, 14 and 28

Trial Locations

Locations (2)

Banner University Medical Center Phoenix; 🇺🇸 Phoenix, Arizona, United States

Banner University Medical Center Tucson; 🇺🇸 Tucson, Arizona, United States