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NCT02609230 · ClinicalTrials.gov registry record · Phase 1
A Dose-Escalation Study of Onc201 Administered Every One or Three Weeks in Advanced Solid Tumors and Multiple Myeloma
A Phase 1 study, sponsored by Fox Chase Cancer Center.
- Completed
- Registry status
- Phase 1
- Development phase
- 33
- Enrollment target
NCT02609230: Completed Phase 1 study, sponsored by Fox Chase Cancer Center.
NCT02609230 is a Phase 1 study that has completed, run by Fox Chase Cancer Center. The registered enrollment target is 33 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02609230, a Phase 1 study, has completed, sponsored by Fox Chase Cancer Center.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 33 participants
- Enrollment target
Study Summary
This study will determine the maximum tolerated dose (MTD) and/or the recommended phase II dose (RP2D) of single agent ONC201 in patients with advanced solid tumors or multiple myeloma.
Interventions
- DRUG ONC-201
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2015-11-05 |
| Est. Completion | 2020-03-26 |
| Phase | Phase 1 |
What the finished NCT02609230 record still lists
NCT02609230 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower).
The record links to 0 conditions, and to 1 intervention - of which ONC-201 is the first listed.
NCT02609230 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02609230 about?
NCT02609230 is a clinical study titled "A Dose-Escalation Study of Onc201 Administered Every One or Three Weeks in Advanced Solid Tumors and Multiple Myeloma". This study will determine the maximum tolerated dose (MTD) and/or the recommended phase II dose (RP2D) of single agent ONC201 in patients with advanced solid tumors or multiple myeloma.
What is the current status of trial NCT02609230?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 33 participants. The study started on 2015-11-05. Estimated completion is 2020-03-26.
What interventions are being tested in trial NCT02609230?
The interventions under investigation include: ONC-201 (DRUG).
Who is sponsoring clinical trial NCT02609230?
This trial is sponsored by Fox Chase Cancer Center, which has 183 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02609230's enrollment target sits among peer trials
33 1280th of 2000 higher than 705 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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