THAI-CARES RSV Study is a Phase II, open-label, multicenter, randomized controlled trial with a two-arm, parallel-group design. The study aims to assess the safety, efficacy, and acceptability of a five-day course of Remdesivir (VEKLURY®) in children under two years of age who are hospitalized with confirmed respiratory syncytial virus (RSV) infection, as determined by either a rapid antigen test or RT-PCR. The primary objectives include evaluating the treatment's safety profile, its ability to significantly reduce RSV replication, and its overall acceptance in this patient population.
An overall target of 120 participants will be involved in the study. Eligible participants will be randomized (1:1) to receive ARM 1: Standard of care alone (control arm). ARM 2: Remdesivir in combination with the standard of care. Remdesivir will be administered by intravenous infusion every 24 hours for five (5) consecutive days. Each participant will be followed during hospitalization plus 7-10 days after Day 6\* for final visit.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
120
Remdesivir (RDV) has shown potent antiviral activity against RSV A in an animal model. Remdesivir has been also shown to be a safe treatment option in pediatric patients hospitalized with COVID-19. Based on previous clinical evidence and preclinical data, to address the unmet medical need for safe and effective RSV therapy, this study is being conducted to investigate remdesivir in infants and children (aged 0 days to \<2 years) as a potential treatment for RSV infection.
Center of Excellence for Pediatric Infectious Diseases and Vaccines Faculty of Medicine, Chulalongkorn University (CE-PID)
Bangkok, Thailand
RECRUITINGNakornping Hospital
Chiang Mai, Thailand
RECRUITINGMaharaj Nakorn Chiang Mai Hospital
Chiang Mai, Thailand
RECRUITINGChiangrai Prachanukroh Hospital
Chiang Rai, Thailand
RECRUITINGKhon Kaen Hospital
Khon Kaen, Thailand
NOT_YET_RECRUITINGLampang Hospital
Lampang, Thailand
RECRUITINGMahasarakham Hospital
Maha Sarakham, Thailand
RECRUITINGSamut Sakhon Hospital
Samut Sakhon, Thailand
NOT_YET_RECRUITINGSafety and tolerability of Remdesivir
Outcome Measures: Occurrence of the following events from the time of randomization until the last study visit: * serious adverse events (SAEs); * adverse events (AEs) of Grade 3 or higher * treatment-related AEs * AEs leading to treatment discontinuation * treatment-related AEs leading to treatment discontinuation * AEs of Grade 3 or higher leading to treatment discontinuation Acceptability of daily remdesivir infusions to children, health care personnel, and caregivers assessed through questionnaires and direct observation.
Time frame: 1 Week
Evaluation of the RSV RNA viral load
Outcome measures: * Reduction in RSV RNA viral load reduction from Day 1 to Day 6, i.e. one day after the end of treatment. * Time from Day 1 to RSV RNA viral load drop below the RT-PCR quantification limit until Day 6. * Area under the RSV RNA viral load-time curve (AUC) from Day 1 until Day 6.
Time frame: 1 Week
Efficacy of Remdesivir
Ourtome Measures: Improvement on the PRESS 6-step ordinal scale from Day 1 until Day 6. PK parameters will be estimated for remdesivir and its metabolites GS-704277 and GS-44152417.
Time frame: 1 Week
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