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Paridiprubart · EB-05

Other · developed by Edesa Biotech

Phase 2 Most advanced trial
EDSA Developer
1 Registered trials

What is Paridiprubart?

Paridiprubart (also coded EB-05 or EB05) is an investigational agent given as a single intravenous dose of 15 mg/kg, up to a maximum of 1440 mg. It is studied in acute respiratory distress syndrome (ARDS).

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as
EB-05
Drug type
Other
Therapy area
Respiratory
Developer
Edesa Biotech Inc. (EDSA)
FDA status
Investigational, not approved in the US. Most advanced trial: Phase 2
UNII
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🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT06703073 Phase 2 Acute Respiratory Distress Syndrome (ARDS) Recruiting EDSA

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Acute Respiratory Distress SyndromeAcute Respiratory Distress Syndrome (ARDS)ARDSARDS (Acute Respiratory Distress Syndrome)

More from Edesa Biotech

Sources

Updated Oct 11, 2026. Something wrong or missing? Report it on the EDSA page.

Follow EDSA, the company behind Paridiprubart

See EDSA's upcoming FDA decisions, trial readouts, cash runway and dilution risk, updated every day from SEC, FDA and ClinicalTrials.gov filings.

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Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

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