Extended Remdesivir Infusion Combined With Nirmatrelvir/Ritonavir for Persistent SARS-CoV-2 Infection in Immunocompromised Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Taiwan University Hospital

About this trial

To evaluate the safety and efficacy of extended remdesivir infusion, targeting on immunocompromised individuals who had positive SARS-CoV-2 PCR despite an oral antiviral agent prescription.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Receive B-cell depletion therapy or bendamustine within 6months

Laboratory confirmed SARS-CoV-2 infection

Symptoms onset within 72 hours

Disqualifiers

Prior use of any anti-SARS-CoV-2 agents within 2 weeks. Remdesivir or NMV/r initiated within 24 hours is acceptable

Life expectancy < 1 month

Previous adverse effect related to remdesivir or NMV/r

Concurrent use medicine with drug-drug interaction with NMV/r

Trial design

Treatments tested in this trial

  • combination therapy
  • SOC

Treatment groups

40 Participants
are divided into 2 treatment groups