Study of TGW101 for Advanced Solid Tumors

This study is testing a new treatment called TGW101 for people with advanced solid tumors. TGW101 is a combination of two parts: TGW101-ADC and TRG001, which are given separately. The main goals are to see how safe TGW101 is, what side effects it might cause, and to find the best dose. Researchers will also look at how the body handles TGW101 and if it shows any early signs of helping against cancer. You may be able to join if you are 18 or older and have a solid tumor that has progressed. The study is currently unclear about its recruitment status.

Study design
This is an interventional study with a planned enrollment of 50 participants. It aims to evaluate the safety, tolerability, and preliminary effectiveness of TGW101.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be monitored for adverse events and cycle delays for up to approximately 10 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06959706

Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of TGW101 in Participants With Advanced Solid Tumors

Recruiting
PHASE1Ages 18+InterventionalTreatment
Tagworks Pharmaceuticals BV
~50 participants
Updated 2026-04-16 on ClinicalTrials.gov
What's tested:TGW101

At a glance

Recruiting sites
7 of 7 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of Participants Experiencing Adverse Events (AEs)
Measured over Up to approximately 10 months
+4 more outcomes measured
Advanced Solid Tumors
7 sites across 5 states
Texas3
Arizona1
Massachusetts1
Pennsylvania1
Virginia1

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  • Number of Participants Experiencing Adverse Events (AEs)Up to approximately 10 months
  • Number of Participants Experiencing Dose-limiting Toxicities (DLTs)Up to Day 21
  • Number of Participants Experiencing Cycle DelayUp to approximately 10 months
  • Number of Participants Experiencing Dose ReductionUp to approximately 10 months
  • RDE of TGW101Up to approximately 10 months