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Cerca in Study Connect

Active, Not Recruiting

Study of Abatacept in the Treatment of Hospitalized COVID-19 Participants With Respiratory Compromise - IM101-873

Aggiornato: 5 agosto, 2021   |   ClinicalTrials.gov

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Dettagli della sperimentazione

  • Phase 2

    Fase

  • Sesso

  • 18+

    Fascia d'età

  • Active, Not Recruiting

Opzioni di trattamento

Bracci dello studio
TERAPIA ASSEGNATA
Experimental: Abatacept + Standard of care
Biological: Abatacept
Placebo Comparator: Placebo infusion + Standard of care
Other: Placebo

Principali criteri di idoneità

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - A confirmed virological diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection (by reverse-transcription polymerase chain reaction (RT-PCR)). - Hospitalized (or in the Emergency Department awaiting a bed after hospitalization) - Respiratory compromise as defined by requirement of oxygen supplementation to maintain oxygen saturation ≥ 93% but not requiring mechanical ventilation - Abnormal chest X-ray consistent with COVID-19 and not indicating other serious medical condition that would serve as an exclusionary criteria - Women and men must agree to follow specific methods of contraception, if applicable Exclusion Criteria: - Women who are breastfeeding - Recent acute infection defined as: i) Any acute infection within 60 days prior to randomization that required hospitalization or treatment with parenteral antibiotics (not COVID-19 related) ii) Any acute infection within 30 days prior to randomization that required oral antimicrobial or antiviral therapy - History of chronic or recurrent bacterial infection (e.g., chronic pyelonephritis, osteomyelitis, bronchiectasis) - Prior exposure to BMS-188667 (abatacept) Other protocol-defined inclusion/exclusion criteria apply

Ti consigliamo vivamente di contattare BMS per segnalare gli effetti collaterali (eventi avversi)
Qui vengono definiti gli effetti collaterali (eventi avversi) e altri eventi da segnalare
Segnala effetti collaterali (eventi avversi) o reclami sulla qualità del prodotto: informazioni mediche

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