CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 25 enrolled
Drug / intervention
WTX-330drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05678998
NCT05678998Phase 1Completed

A Phase 1 (First-In-Human [FIH]), Multi-Site, Dose Escalation and Expansion Study of WTX-330 in Adult Patients With Advanced or Metastatic Solid Tumors or Lymphoma

Werewolf Therapeutics, Inc.·interventional·Posted Jan 10, 2023·Updated Jan 6, 2026

In Brief

A Phase 1 clinical trial evaluating WTX-330 for Advanced or Metastatic Solid Tumors and Non-Hodgkin Lymphoma. Completed, enrolled 25 participants across 9 sites.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
2023202420252026
First PostedJan 10, 2023
Enrollment StartDec 6, 2022
Primary CompletionDec 23, 2024
Study CompletionFeb 5, 2025
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 3.5 years ago

Interventions

WTX-330drug

Investigation Product