drugset / Trial / NCT05678998

WTX-330 in Patients With Advanced or Metastatic Solid Tumors or Non-Hodgkin Lymphoma

NCT05678998 ↗

Phase 1 Completed 25 enrolled Werewolf Therapeutics, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

A first-in-human, Phase 1, open-label, multicenter study of WTX-330 administered as a monotherapy to patients with advanced or metastatic solid tumors or non-Hodgkin lymphoma.

Timeline

Start
2022-12-06
Primary completion
2024-12-23
Completion
2025-02-05

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

release “announced initial safety and efficacy data from its ongoing Phase 1 clinical trial of WTX-330” werewolftx.com ↗

release “Preliminary clinical findings presented at SITC demonstrate WTX-330’s promising therapeutic potential as a monotherapy, exhibiting a favorable tolerability profile and inducing tumor shrinkage” werewolftx.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject WTX-330 Protein / enzyme biologic — —

Indications