Status:
UNKNOWN
Epidemiology of SARS-CoV-2 and Mortality to Covid19 Disease in French Cancer Patients
Lead Sponsor:
Gustave Roussy, Cancer Campus, Grand Paris
Conditions:
Cancer & COVID 19
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
To determine the prevalence and the 3-months incidence of SARS-CoV-2 in cancer patients (Part A). To evaluate the Covid-19 disease-specific mortality rate in cancer patients treated by hydroxychloroq...
Eligibility Criteria
Inclusion
- All types of locally advanced and metastatic malignancy
- Male/female participants
- Age\>18 y.o.
- Signed informed consent for participation in the study
- No restriction on Eastern Cooperative Oncology Group (ECOG)/World Health Organization (WHO) Performance Status
- Subject should not have received a prior systemic anti-viral treatment for Covid19 disease.
Exclusion
- Patients with known hypersensitivity to hydroxychloroquine or chloroquine, azithromycin, erythromycin, or any other macrolide, ketolide or any of the excipients of the hydroxychloroquine and/or azithromycin-based specialty used.
- Severe hepatic impairment and patients with severe cholestasis.
- Patients with renal insufficiency with creatinine clearance \< 40 mL/min.
- Combinations of drugs contraindicated in accordance with the approvals of the specialties used.
- Patients currently treated with Tamoxifen
- Patients already treated by hydroxychloroquine or azithromycin for Covid19 disease or currently treated with other antiviral drugs against coronavirus.
- Patients with known contra-indication to treatment with the study drug, including retinopathy, G6PD deficiency, QT prolongation and severe hepato-cellular insufficiency.
- Patients post allogeneic hematopoietic stem cell transplantation are eligible to the Part B treatments but the potential toxic effects of hydroxychloroquin and azithromycin on hematopoietic stem cells should be taken into consideration by prescribers.
- Pregnant or breastfeeding women. Women of childbearing potential (WOCBP, as defined in appendix 2) should have a negative urine or serum pregnancy test within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
Key Trial Info
Start Date :
April 3 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2022
Estimated Enrollment :
1000 Patients enrolled
Trial Details
Trial ID
NCT04341207
Start Date
April 3 2020
End Date
April 1 2022
Last Update
April 10 2020
Active Locations (1)
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1
Gustave Roussy
Villejuif, Val De Marne, France, 94800