Dose Escalation & Expansion Study of Oral VRx-3996 & Valganciclovir in Subjects With EBV+ Lymphoid Malignancies

Completed · Phase 1/Phase 2

Conditions studied: Epstein-Barr Virus-Associated Lymphoma, Lymphoproliferative Disorders

In brief

A two part, Phase 1b/2 study to define a recommended Phase 2 dose of VRx-3996 in combination with valganciclovir (Phase 1b) designed to evaluate the efficacy of this combination in relapsed/refractory Epstein-Barr Virus Associated Lymphoma (EBV+ lymphomas).

Key facts

Study ID
NCT03397706
Run by
Viracta Therapeutics, Inc.
People needed
64
Starts
2018-03-29
Expected to finish
2023-05-04
Last updated by the study team
2025-03-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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