Status:
UNKNOWN
Study to Assess Efficacy and Safety Relative to Standard of Care in Patients With COVID-19 Pneumonia
Lead Sponsor:
Angion Biomedica Corp
Collaborating Sponsors:
CTI Clinical Trial and Consulting Services
Conditions:
COVID-19
Pneumonia
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
To assess the clinical efficacy of ANG-3777 relative to the standard of care in reducing the severity and progression of pulmonary and renal dysfunction and mortality in adult patients hospitalized wi...
Eligibility Criteria
Inclusion
- Patient is a male or nonpregnant female 18 years of age or older.
- Patient has a positive reverse-transcriptase-polymerase-chain-reaction (RT-PCR) assay for SARS-CoV-2 in a respiratory tract sample during the current hospital admission.
- Patient has pneumonia confirmed by chest imaging.
- Patient has moderate to severe disease based on the WHO disease severity scale assessment at the time of randomization defined as:
- Score 4, only those with FiO2 \> 40%
- Score 5 (Non-invasive ventilation or high-flow oxygen)
- Patient has ability to provide informed consent signed by study patient or legally acceptable representative.
- Patient has willingness and ability to comply with study-related procedures/assessments
Exclusion
- Has an active malignancy or history of solid or hematological malignancies within 5 years prior to enrollment in the study. Patients who had basal or squamous cell carcinoma-in-situ of the skin that was diagnosed \> 2 years prior to the study enrollment and not currently being treated are eligible for study enrollment.
- Patient is pregnant or breast-feeding.
- Patient, in the opinion of the investigator, is unlikely to survive for ≥48 hours from the time of screening.
- Patient has any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the patient by their participation in the study.
- Patient with alanine aminotransferase (ALT) or aspartate transaminase (AST) \> 3x upper limit of normal (ULN) and/or total bilirubin \> 2xULN at baseline
- Patient requires treatment with the cytochrome P450 1A2 (CYP1A2) inhibitors, ciprofloxacin (Cipro®) and/or fluvoxamine (Luvox®)
- Patients participating in any other clinical trial with an investigational drug product or procedure
- Recipients of solid organ and/or hematopoietic cell transplantation
- Patient is known to have End Stage Renal Disease (ESRD) and was being treated with maintenance hemodialysis or peritoneal dialysis prior to the current hospitalization.
- Note: Patients who initiated RRT due to Acute Kidney Injury during their current hospitalization will be eligible for the study
Key Trial Info
Start Date :
July 31 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 30 2021
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT04459676
Start Date
July 31 2020
End Date
April 30 2021
Last Update
April 15 2021
Active Locations (10)
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1
Hospital Vera Cruz - NUPEC Nucleo de Pesquisa Clínica
Belo Horizonte, Minas Gerais, Brazil
2
Santa Casa de Misericórdia de Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil
3
Pontifícia Universidade Catolica de Campinas
Campinas, São Paulo, Brazil
4
UPCLIN - Faculdade de Medicina da UNESP Campus de Botucatu
Botucatu, Brazil