Latest1 information on COVID-19
©2022 Stanford Medicine
Recruiting
Trial ID: NCT04924660
CONNECTS Master Protocol for Clinical Trials Targeting Macro-, Micro-immuno-thrombosis, Vascular Hyperinflammation, and Hypercoagulability and Renin-angiotensin-aldosterone System (RAAS) in Hospitalized Patients With COVID-19 (ACTIV-4 Host Tissue)
Associate Professor of Medicine (Pulmonary and Critical Care Medicine)
Inclusion criteria
1. Hospitalized for COVID-19
2. ≥18 years of age
3. SARS-CoV-2 infection, documented by:
1. a nucleic acid test (NAT) or equivalent testing within 3 days prior to
randomization OR
2. documented by NAT or equivalent testing more than 3 days prior to randomization
AND progressive disease suggestive of ongoing SARS-CoV-2 infection per the
responsible investigator (For non-NAT tests, only those deemed with equivalent
specificity to NAT by the protocol team will be allowed. A central list of
allowed non- NAT tests is maintained in Appendix E. Appendix E. Non-NAT Tests
Deemed with Equivalent Specificity to NAT by the Protocol Team).
4. Hypoxemia, defined as SpO2 <92% on room air, new receipt of supplemental oxygen to
maintain SpO2 ≥92%, or increased supplemental oxygen to maintain SpO2 ≥92% for a
patient on chronic oxygen therapy
5. Symptoms or signs of acute COVID-19, defined as one or more of the following:
1. cough
2. reported or documented body temperature of 100.4 degrees Fahrenheit or greater
3. shortness of breath
4. chest pain
5. infiltrates on chest imaging (x-ray, CT scan, lung ultrasound)
Exclusion criteria
1. Onset of COVID-19 symptom fulfilling inclusion criterion #5 >14 days prior to
randomization
2. Hospitalized with hypoxemia (as defined in inclusion #4) for >72 hours prior to
randomization (the 72-hour window for randomization begins when the patient first
meets the hypoxemia inclusion criteria after hospital admission)
3. Pregnancy
4. Breastfeeding
5. Prisoners
6. End-stage renal disease (ESRD) on dialysis
7. Patient undergoing comfort care measures only such that treatment focuses on
end-of-life symptom management over prolongation of life.
8. The treating clinician expects inability to participate in study procedures or
participation would not be in the best interests of the patient
9. Known allergy/hypersensitivity to IMP or its excipients
The following exclusion criteria differ from the master protocol criteria:
TXA127-specific exclusion criteria(4/20/2022 Closed to Accrual):
1. Patient unable to participate or declines participation in the TXA127/Ang(1-7) arm.
2. History of sensitivity (including angioedema) or allergic reaction to medication
targeting the RAAS system including study medications or other allergy in the opinion
of the investigator that contraindicates participation (not applicable to fostamatinib
arm)
3. Hemodynamic instability - defined as MAP < 65 mmHg at time of randomization confirmed
on two measurements 5 minutes apart OR vasopressors at or above norepinephrine
equivalent of 0.1 mcg/kg/min in prior 4 hours to maintain MAP > 65 mmHg.
4. Known severe renal artery stenosis.
5. Known significant left ventricular outflow obstruction, such as obstructive
hypertrophic cardiomyopathy or severe aortic or mitral stenosis.
6. Randomized in another trial evaluating RAAS modulation in the prior 30 days
TRV027-specific exclusion criteria (4/20/2022 Closed to Accrual):
1. Participants on ARBs will be excluded from this study arm.
2. Patient unable to participate or declines participation in the TRV027 arm.
3. History of sensitivity (including angioedema) or allergic reaction to medication
targeting the RAAS system including study medications or other allergy in the opinion
of the investigator that contraindicates participation (not applicable to fostamatinib
arm)
4. Hemodynamic instability - defined as MAP < 65 mmHg at time of randomization confirmed
on two measurements 5 minutes apart OR vasopressors at or above norepinephrine
equivalent of 0.1 mcg/kg/min in prior 4 hours to maintain MAP > 65 mmHg.
5. Known severe renal artery stenosis.
6. Known significant left ventricular outflow obstruction, such as obstructive
hypertrophic cardiomyopathy or severe aortic or mitral stenosis.
7. Randomized in another trial evaluating RAAS modulation in the prior 30 days
Fostamatinib specific exclusion criteria:
The following exclusion criteria differ from the master protocol criteria:
1. Randomized in another trial evaluating fostamatinib in the prior 30 days
Study arm exclusion criteria measured within 24 hours prior to randomization:
1. AST or ALT ≥ 5 × upper limit of normal (ULN) or ALT or AST ≥ 3 × ULN and total
bilirubin ≥ 2 × ULN
2. SBP > 160 mmHg or DBP > 100 mmHg at the time of screening and randomization
3. ANC < 1000/mL
4. Patient is anticipated to require a strong CYP3A inhibitor (Atazanavir, Certinib,
Clarithromycin, Cobicistat and cobicistat-containing coformulations,
Idelalisib,Indinavir, Itraconazole, Ketoconazole, Levoketoconazole, Lonafarnib,
Lopinavir, Mifeprostone, Mibefradil, Nefazodone, Nelfinavir,
Ombitasvir-paritaprevir-ritonavir plus dasabuvir, Posaconazole, Ribociclib Ritonavir,
Saquinavir, Telithromycin, Troleandomycin, Tucatinib, Voriconazole) from randomization
to 21 days post-randomization. For a full list of CYP3A4 substrates, please reference
this regularly updated list: https://drug-interactions.medicine.iu.edu/MainTable.aspx.
5. Patient unable to participate or declines participation in the fostamatinib arm.
drug: Fostamatinib
drug: TXA127
drug: TRV027
drug: Placebo
Recruiting
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