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Rademikibart · CBP-201

Other · developed by Connect Biopharm LLC

Phase 2 Most advanced trial
CNTB Developer
1 Registered trials

What is Rademikibart?

Rademikibart (CBP-201) is an agent given as a single 300 mg intravenous push over about 2 minutes.

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

At a glance

Also known as
CBP-201
Drug type
Other
Therapy area
Respiratory
Developer
Connect Biopharm LLC (CNTB)
FDA status
Investigational, not approved in the US. Most advanced trial: Phase 2
UNII
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🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT07705737 Phase 2 Asthma Acute Recruiting CNTB

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

Conditions studied

Asthma AcuteCOPD Exacerbation Acute

More from Connect Biopharm LLC

Sources

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

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See CNTB'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

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.