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HOWL US Equity

Werewolf Therapeutics, Inc.Health Care · Pharmaceutical Preparations · CIK 1785530 · FY ends Dec 31
$0.41
+0.00 (+0.12%)
USD · as of 2026-08-17 · marketstack
3 registered studies · 2 active

Studies where HOWL is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

3 interventional · 1 with posted results

Held by 6 tracked-famous managers (Balyasny Asset Management L.P., RENAISSANCE TECHNOLOGIES LLC, JANE STREET GROUP, LLC, Squarepoint Ops LLC, MILLENNIUM MANAGEMENT LLC, +1 more) · FINRA short interest 1.3 days to cover (settled 2026-07-31) · insider 90d: 0 buys / 28 sells · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
A Phase 1b/2 Multisite Dose-finding and Expansion Study of WTX-330 in Adult Patients With Selected Advanced or Metastatic Solid Tumors or LymphomaNCT06939283Incidence of Dose Limiting Toxicities (DLTs)Non-randomized · Open-label · TreatmentPhase 1/2Active, not recruitingDrug: WTX-330Advanced or Metastatic Solid Tumors, Non-Hodgkin Lymphoma100Aug 2028≤ 743 d2026-02-10
Dose Escalation and Expansion Study of WTX-124 as Monotherapy and in Combination With Pembrolizumab (Pembro) in Patients With Selected Advanced or Metastatic Solid TumorsNCT05479812Incidence of Dose Limiting Toxicities (DLTs) in monotherapy and combination therapyNon-randomized · Open-label · TreatmentPhase 1Active, not recruitingDrug: WTX-124, pembrolizumabMetastatic Solid Tumor, Advanced Solid Tumor1502026-07-012026-02-09
WTX-330 in Patients With Advanced or Metastatic Solid Tumors or Non-Hodgkin LymphomaNCT05678998results2026-01-06Incidence of Dose Limiting Toxicities (DLTs)Non-randomized · Open-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 1CompletedDrug: WTX-330Advanced or Metastatic Solid Tumors, Non-Hodgkin Lymphoma252024-12-23actual2026-01-06

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19