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NCT02160106 · ClinicalTrials.gov registry record · Phase 1
First in Human Dose Escalation Study of Vactosertib (TEW-7197) in Subjects With Advanced Stage Solid Tumors
A Phase 1 study, sponsored by MedPacto.
- Completed
- Registry status
- Phase 1
- Development phase
- 35
- Enrollment target
NCT02160106: Completed Phase 1 study, sponsored by MedPacto.
NCT02160106 is a Phase 1 study that has completed, run by MedPacto. The registered enrollment target is 35 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02160106, a Phase 1 study, has completed, sponsored by MedPacto.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 35 participants
- Enrollment target
Study Summary
The phase I dose escalation study will investigate the safety, tolerability, and pharmacokinetics of the TGF-β pathway inhibitor TEW 7197 in subjects with advanced, refractory solid tumors.
Interventions
- DRUG TEW-7197
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2014-07-29 |
| Est. Completion | 2018-08-28 |
| Phase | Phase 1 |
What the finished NCT02160106 record still lists
NCT02160106 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower).
The record links to 0 conditions, and to 1 intervention - of which TEW-7197 is the first listed.
NCT02160106 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02160106 about?
NCT02160106 is a clinical study titled "First in Human Dose Escalation Study of Vactosertib (TEW-7197) in Subjects With Advanced Stage Solid Tumors". The phase I dose escalation study will investigate the safety, tolerability, and pharmacokinetics of the TGF-β pathway inhibitor TEW 7197 in subjects with advanced, refractory solid tumors.
What is the current status of trial NCT02160106?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 2014-07-29. Estimated completion is 2018-08-28.
What interventions are being tested in trial NCT02160106?
The interventions under investigation include: TEW-7197 (DRUG).
Who is sponsoring clinical trial NCT02160106?
This trial is sponsored by MedPacto, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02160106's enrollment target sits among peer trials
35 1258th of 2000 higher than 728 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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