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Zaloblideg · ARV-393

Small molecule (PROTAC degrader) · Degrader of BCL6 · developed by Arvinas

Phase 1 Most advanced trial
ARVN Developer
1 Registered trials

What is Zaloblideg?

Zaloblideg is an orally bioavailable PROTAC degrader that targets BCL6 for proteasome-mediated degradation. It binds BCL6 on tumor cells while recruiting E3 ubiquitin ligase, inducing BCL6 degradation and inhibiting downstream survival pathways. It is studied in relapsed/refractory mature B-cell non-Hodgkin lymphoma and angioimmunoblastic T-cell lymphoma.

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

At a glance

Also known as
ARV-393
Drug type
Small molecule (PROTAC degrader)
Targets
BCL6, E3 ubiquitin ligase (binding partner it blocks)
Mechanism
Degrader of BCL6
Pathways
proteasome-mediated degradation, BCL6-mediated signaling
Therapy area
Oncology
Developer
Arvinas Inc. (ARVN)
FDA status
Investigational, not approved in the US. Most advanced trial: Phase 1
UNII
4YM2ENK9TD

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT06393738 Phase 1 Relapsed/Refractory (R/R) Mature B Cell Non Hodgkin Lymphoma (NHL) Recruiting ARVN

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

More from Arvinas

Sources

Updated Oct 3, 2026. Something wrong or missing? Report it on the ARVN page.

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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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