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BetaBart

Radiopharmaceutical

Phase 1/2 Most advanced trial
1 Registered trials

What is BetaBart?

BetaBart is a radiopharmaceutical combining lutetium-177 (177Lu) with unlabeled BetaBart, administered intravenously at escalating doses every 6 weeks. It is being studied in multiple solid tumors including prostate, colorectal, lung, ovarian, cervical, endometrial, breast, head and neck, esophageal, and sarcoma cancers.

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

At a glance

Drug type
Radiopharmaceutical
Therapy area
Oncology
In trials of
MEDP
FDA status
Investigational, not approved in the US. Most advanced trial: Phase 1/2

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT07189871 Phase 1/2 Castration-Resistant Prostate Cancer (CRPC) Recruiting MEDP

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

Conditions studied

Castration-Resistant Prostate Cancer (CRPC)Cervical CancerColorectal CancerEndometrial CancerEsophageal Squamous Cell Carcinoma (ESCC)Head &Amp; Neck Squamous Cell Carcinoma (HNSCC)NSCLC (Non-small Cell Lung Cancer)Ovarian CancerSarcomaSmall Cell Lung Cancer (SCLC )TNBC, Triple Negative Breast Cancer

Sources

Updated Oct 3, 2026.

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.