OPtimisation of Antiviral Therapy in Immunocompromised COVID-19 Patients: a Randomized Factorial Controlled Strategy Trial: the OPTICOV Study
Overview
- Phase
- Phase 2
- Intervention
- Paxlovid 5 days
- Conditions
- COVID-19
- Sponsor
- ANRS, Emerging Infectious Diseases
- Enrollment
- 256
- Locations
- 18
- Primary Endpoint
- Percentage of patients with SARS-CoV-2 viral load (threshold cicle (Ct) <32) by real-time RT-PCR in nasopharyngeal swabs at Day 10 after treatment initiation.
- Status
- Recruiting
- Last Updated
- 2 months ago
Overview
Brief Summary
The overall purpose of the trial is to evaluate the efficacy and safety of possible combination antiviral therapy DAA (remdesivir + nirmatrelvir/r)∞ versus the reference monotherapy (nirmatrelvir/r alone) and to assess the efficacy and safety of increasing the nirmatrelvir/r course from 5- to 10 days in immunocompromised patients diagnosed with asymptomatic or mild to moderate COVID-19.
Detailed Description
This is a randomized, controlled, factorial, superiority trial to evaluate the viral efficacy of DAA (nirmatrelvir/r) + DAA (remdesivir)∞ versus nirmatrelvir/r alone and of 5 days versus 10 days of nirmatrelvir/r in immunocompromised patients diagnosed with asymptomatic or mild to moderate COVID-19. The primary objective is to assess whether (i) a combination antiviral therapy of two DAA (nirmatrelvir/r + remdesivir)∞ And/or (ii) an increase in nirmatrelvir/r duration from 5 to 10 days improves viral efficacy by decreasing the SARS-CoV-2 positivity rate by real time RT-PCR (CT\<32) in nasopharyngeal swabs at D10. Patients will be eligible if they are immunocompromised, have confirmed asymptomatic SARS-CoV-2 infection or mild to moderate COVID-19, regardless of symptoms onset, provided that they have no contra-indication to any of the study drugs. A total of 256 patients will be included in France and Switzerland. Participants not eligible for randomisation or who refuse to participate to the trial for any reason will be proposed to be included in an exploratory non comparative cohort (maximum 97 participants).
Investigators
Alexandra Calmy
HIV/AIDS Unit Director
University Hospital, Geneva
Eligibility Criteria
Inclusion Criteria
- •Laboratory confirmed SARS-CoV-2 infection by RT-PCR or positive antigenic test (commercialized assay)
- •Asymptomatic or mild to moderate COVID-19 (WHO progression scale \<
- •Patients receiving oxygen therapy for reasons other than a pulmonary COVID-19 are eligible).
- •≥ 16 years of age (for patients recruited in Italy and in Norway, ≥ 18 years of age);
- •Immunocompromised as defined by ≥ 1 risk factors for severe COVID-19 as assessed by the FOPH list (criteria 5: diseases/treatments leading to immune suppression) or other immunosuppression criteria such as Severe immunosuppression (e.g., HIV infection with CD4 + T cell count \<350 / µl) Neutropenia (\<1000 neutrophils / µl) ≥1 week Lymphocytopenia (\<200 lymphocytes/µl) On dialysis treatment Hereditary immunodeficiencies Intake of drugs which suppress the immune system (e.g. glucocorticoids for a long time \[an equivalent dose of prednisone \>20 mg/day \> 3 months\], monoclonal antibodies, cytostatics, biological products, everolimus, mTOR inhibitors etc.) in the last 12 months Active cancer under cytostatics or targeted therapy known to be immunosuppressive (e.g., platinum salts, cyclophosphamide, anthracyclines, taxanes, 5-fluorouracil, gemcitabine, purine inhibitors, proteasome inhibitors) or associated with hematologic toxicity (neutropenia, lymphopenia), for example sunitinib, imatinib, regorafenib. Aggressive lymphomas (all types) Acute lymphatic leukemia Acute myeloid leukemia Acute promyelocytic leukemia T prolymphocytic leukemia Primary central nervous system lymphoma Stem cell transplantation Light chain amyloidosis Chronic lymphoid leukemia Multiple myeloma Sickle cell disease Bone marrow transplant Organ transplant Being on the waiting list for an organ transplant
- •Willing and able to comply with study requirements and restrictions as described in the informed consent form (ICF)
- •Enrolled in or a beneficiary of a Social Security program (State Medical Aid (AME) is not a Social Security program) or holders of health insurance (LAF for participants recruited in Norway).
- •Participant's or its legal representative's signature of the informed consent form
Exclusion Criteria
- •SARS-CoV-2 PCR ≥30 CT at screening
- •Hypersensitivity to study drugs (active substance(s) or excipients)
- •Body weight \< 40 kg
- •AST and/or ALT \> 5 times the upper limit
- •Cirrhosis Child-Pugh score C
- •Is taking or is anticipated to require any prohibited therapies\*.
- •Participation in another interventional clinical study with an investigational compound or device, including COVID-19 therapeutics, where the study intervention is performed in the 28 days preceding the inclusion and the 10 days after the inclusion. Investigators of the different clinical studies should agree on participant's inclusion.
- •Presence of any condition for which, in the opinion of the investigator, participation would not be in participant's best interest or that could prevent, limit, or confound the protocol-specified assessments
- •Having received antiviral treatments against SARS-CoV-2 in the 14 days before the inclusion with exception of those having received one or two doses of nirmatrevir/r in the 24h preceding the inclusion in the study.
- •Pregnant or breastfeeding female
Arms & Interventions
Nirmatrelvir/r 5 days alone
Intervention: Paxlovid 5 days
Nirmatrelvir/r 10 days alone
Intervention: Paxlovid 10 days
Nirmatrelvir/r 5 days + remdesivir s.d
Intervention: Paxlovid 5 days
Nirmatrelvir/r 5 days + remdesivir s.d
Intervention: Veklury
Nirmatrelvir/r 10 days + remdesivir s.d
Intervention: Paxlovid 10 days
Nirmatrelvir/r 10 days + remdesivir s.d
Intervention: Veklury
Outcomes
Primary Outcomes
Percentage of patients with SARS-CoV-2 viral load (threshold cicle (Ct) <32) by real-time RT-PCR in nasopharyngeal swabs at Day 10 after treatment initiation.
Time Frame: Day 10
SARS-CoV-2 viral load is measured in nasopharyngeal swabs by real-time RT-PCR
Secondary Outcomes
- Percentage of patients with SARS-CoV-2 viral load (threshold cicle <32 CT) by real-time RT-PCR in nasopharyngeal swabs at Day5, Day14 and Day21 after treatment initiation(Day5, Day14 and Day21)
- Decrease of SARS-CoV-2 viral load measured by copies/ml by nasopharyngeal swab at Day5, Day10, Day14, Day21 and in blood samples at Day5, Day10 and Day14 comparatively to screening(Day5, Day10, Day14, Day21)
- Rate of Post-COVID19 condition at Day90 according to the WHO October 2021 definition(Day 90)
- Percentage of patients with detectable SARS-CoV-2 viremia at Day5, Day10 and Day14(Assessed for 14 days from the date of randomisation at Day5, Day10 and Day14)
- Absence of ability to cultivate virus from viral cultures from nasopharyngeal swabs at Day5, Day10 and Day21(Day5, Day10 and Day21)
- Percentage of patients with sustained resolution or abatement of symptoms defined as a FLU-PRO-Plus score ≤1 at Day5, Day10, Day14, Day21 and Day28(Day5, Day10, Day14, Day21 and Day28)
- Number of de novo emergence of mutations on nasopharyngeal RT-PCR at Day5, Day10, Day14 and Day21 comparatively to screening(Day5, Day10, Day14 and Day21)
- Percentage of participants with an adverse event (AE) or serious adverse event (SAE) or AE leading to treatment discontinuation up to Day28(Day 28)
- Adherence to nirmatrelvir/r with patient-reported adherence and nirmatrelvir/r residual plasma dosage at Day5 and Day10(Day5 and Day10)
- Number of DDIs who led to dosage adjustment of other patient's drugs(Assessed up to Day 10 from randomisation)
- Immunosuppressors residual concentrations, if applicable(as needed)
- Time to first negative SARS-CoV-2 RT-PCR (CT<32) until Day90(Day90)
- To assess the phenotypic resistance (IC50 increase) against treatment for viral strains cultured from nasopharyngeal swabs(Day5, Day10, Day14, Day21)
- All-cause hospitalization and/or death at Day28(Day28)
- Hospitalization at Day28(Day28)
- Death at Day28(Day28)
- Percentage of patients with specific retreatment patients (by antiviral antiinflammatory drugs or convalescent plasma through Day90(Day90)