Last update 21 Nov 2024

USB-002

Overview

Basic Info

Drug Type
Synthetic peptide
Synonyms
Target-
Mechanism-
Therapeutic Areas
Infectious DiseasesRespiratory Diseases
Active Indication-
Inactive Indication
COVID-19Respiratory Distress Syndrome, Adult
Originator Organization
La Jolla Pharmaceutical Co.La Jolla Pharmaceutical Co.
Active Organization-
Inactive Organization
US Biotest, Inc.US Biotest, Inc.
Drug Highest PhaseDiscontinuedPhase 2
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with USB-002
NCT04778059 / TerminatedPhase 2
Phase 2 Trial to Evaluate the Safety, Tolerability, and Preliminary Efficacy of Intravenous USB002 to Treat Patients With Respiratory Distress Due to COVID-19 Infection
100 Clinical Results associated with USB-002
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100 Translational Medicine associated with USB-002
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100 Patents (Medical) associated with USB-002
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100 Deals associated with USB-002
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
COVID-19Phase 2
US
US Biotest, Inc.US Biotest, Inc.
27 Jul 2021
Respiratory Distress Syndrome, AdultPhase 2
US
US Biotest, Inc.US Biotest, Inc.
27 Jul 2021
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
NCT04778059 (CTgov)
Phase 2
COVID-19 | Respiratory Distress Syndrome, Adult
21
Placebo
pglazqrnge(cmhupgigcd) = fgybswhpkv ummmufhnca (cjeyayqdmy, bnqgmawmvy - rsazfvarxt)
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-
01 Dec 2023
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Approval

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Regulation

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