HomeTrialNCT06393738
NCT06393738Phase 1RECRUITING

A Study of ARV-393 in Relapsed/Refractory Non-Hodgkin Lymphoma.

Study Summary

This clinical trial is studying the safety and potential anti-tumor activity of an investigational drug called ARV-393 in patients diagnosed with advanced Relapsed/Refractory non-Hodgkin's lymphoma (R/R NHL) to determine if ARV-393 may be a possible treatment option. ARV-393 is thought to work by breaking down a protein present in many types of non-Hodgkins lymphomas, which may prevent, slow or stop tumor growth. This is the first time ARV-393 will be used by people. The investigational drug will be given as an oral tablet.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment255 participants
Primary Completion
Lead SponsorArvinas Inc.
Data Retrieved2026-04-11 02:54:34.305742+00:00
What This Trial Means for Biotech Investors
Trial Phase Context

Phase 1 trials primarily test safety and dosing in a small number of participants (typically 20–100). Results do not yet speak to efficacy. FDA approval is typically many years away from this stage.

Status & Expected Data

Currently recruiting: the trial is enrolling patients. A data readout is not expected until after enrollment closes and the follow-up period is complete.

Enrolled: 255 participants
Sponsor Catalyst Profile

Arvinas Inc (ARVN) is the sponsoring company for this trial. BiotechSign currently grades this company D (37/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

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