Last updated: August 5, 2022
Sponsor: University of Southern California
Overall Status: Trial Not Available
Phase
2
Condition
Covid-19
Treatment
N/AClinical Study ID
NCT04830735
0S-20-5
0S-20-5
NCI-2020-04367
P30CA014089
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients must have laboratory test proven COVID19 and symptomatic disease requiringhospitalization: virological diagnosis of Sars-CoV2 infection (polymerase chainreaction [PCR]) within 14 days
- Able to sign informed consent for participation in the study
- Subject is hospitalized with one or more of the following:
- Moderate disease: peripheral capillary oxygen saturation (SpO2) >= 93% on roomair with one of the following risk factors for developing severe disease: age >= 60 years, history of hypertension, diabetes mellitus, cardiac disease, chroniclung disease, obesity (calculated body mass index [BMI] >= 30 kg/m^2), andcardiovascular disease, clinical and/or radiological evidence of chestinvolvement, CRP > 2X upper limit of normal, doubling of CRP in 24 hours wherechest findings and CRP elevation not explained by other underlying disease. After the first interim analysis, we may allow enrollment of severe disease COVID infectedpatients if safety and efficacy analysis appears favorable:
- Severe disease:
- Respiratory rate >= 30 breaths/ minute (min)
- SpO2 < 93% while breathing room air
- Partial pressure of oxygen measurement (PaO2)/fraction of inspired oxygen (FiO2) =< 300 mmHg
- Absolute neutrophil count (ANC) > 1000 (baseline blood counts)
- Platelets > 50,000 / mmc (baseline blood counts)
- Alanine aminotransferase/aspartate aminotransferase (ALT/AST) < 5 times theupper limit of the normality
- Total bilirubin < 3 x institutional upper limit of normal (IULN)
- Creatinine < 2.5 times the upper limit of the normality
- Azithromycin allowed but if on both drugs patient should be on constantcardiovascular (CV) monitoring
- Subject must understand and voluntarily sign an informed consent form (ICF)prior to any study-related assessment/procedures being conducted
- Subject is willing and able to adhere to the study visit schedule and otherprotocol requirements
Exclusion
Exclusion Criteria:
- Pleural effusion > grade 2 evident on chest x-ray (CXR) or chest computed tomography (CT)
- Intubation/mechanical ventilation
- Known hypersensitivity to dasatinib
- Patient being treated with immunomodulators or anti-rejection drugs
- Known active infections or other clinical condition that contraindicate dasatinib andcannot be treated or solved according to the judgement of the clinician
- ALT/AST > 5 times the upper limit of the normality
- Total bilirubin > 3 x IULN
- Neutrophils < 1000 / mmc unless; platelets < 50,000 / mmc
Study Design
Study Start date:
August 05, 2022
Estimated Completion Date:
December 15, 2024
Study Description
Connect with a study center
USC / Norris Comprehensive Cancer Center
Los Angeles, California 90033
United StatesSite Not Available
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.