Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:24 PM
Ignite Modification Date:
2025-12-24 @ 7:24 PM
NCT ID:
NCT04707703
Eligibility Criteria:
Inclusion Criteria:
* Written informed consent obtained from the patient or his/her legally authorized person.
* Adult patient (\> 18 years).
* PCR-confirmed SARS-CoV-2 based on nasopharyngeal swab (NPS), oropharyngeal swab (OPS), tracheal aspirate (TA), bronchial aspirate (BA), or bronchoalveolar lavage fluid (BALF) within 14 days prior to ICU admission or within 72 hours following ICU admission.
* Radiographic imaging consistent with SARS-CoV-2 infection (e.g. atypical pneumonia, organizing pneumonia, ground glass opacities) or acute respiratory distress syndrome (ARDS) within 7 days of diagnosis of SARS-CoV-2 infection.
* A negative pregnancy test in women of child-bearing age.
* If a woman is of child-bearing age, she must be willing to use an effective method of contraception for 28 days after the final dose of isavuconazole per manufacturer instructions
Exclusion Criteria:
* Anticipated transfer to another medical center that is not a study site within hours of admission to the ICU.
* Pregnancy based on a positive human chorionic gonadotropin (HCG) test from serum or urine.
* Patient who is breastfeeding and unable to discontinue breastfeeding while taking the study drug.
* Patients with a diagnosis of invasive aspergillosis/detection of Aspergillus spp. by culture from sputum, TA, BA, or BALF or positive GM from serum or BALF at time of screening or randomization.
* History of invasive aspergillosis within the prior six months.
* Patients with a known intolerance or hypersensitivity to isavuconazole or other azole agents.
* History of familial short QT syndrome.
* Patients that are being treated with mold-active antifungal agents for invasive aspergillosis or another invasive fungal infection.
* Patients with severe hepatic impairment or liver cirrhosis (Child C) should be excluded from the study unless the treating physicians feel the benefits of treatment outweigh the risks.
* Treatment with Lopinavir/ritonavir for HIV infection.
* Prohibited Medications
* Co-administration with a strong CYP3A4 inhibitor or high-dose ritonavir as they may alter the plasma concentration of isavuconazole.
* Co-administration with a strong CYP3A4 inducer such as rifampin, carbamazepine, St. John's wort, or long acting barbiturates.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04707703
Study Brief:
Protocol Section:
NCT04707703