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NCT03780517 · ClinicalTrials.gov registry record · Phase 1
Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors
A Phase 1 study, sponsored by Boston Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 117
- Enrollment target
NCT03780517: Completed Phase 1 study, sponsored by Boston Pharmaceuticals.
NCT03780517 is a Phase 1 study that has completed, run by Boston Pharmaceuticals. The registered enrollment target is 117 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03780517, a Phase 1 study, has completed, sponsored by Boston Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 117 participants
- Enrollment target
Study Summary
This study will be conducted to assess the safety and tolerability of BOS172738 when administered to patients with advanced solid tumors with rearranged during transfection (RET) gene alterations and also to establish the maximum tolerated dose (MTD) and/or recommended phase 2 dose (RP2D) of BOS172738.
Interventions
- DRUG BOS172738
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 117 participants |
| Start Date | 2018-12-12 |
| Est. Completion | 2023-09-26 |
| Phase | Phase 1 |
What the finished NCT03780517 record still lists
NCT03780517 is an interventional study that assigns participants to a tested intervention. The registered 117 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% higher).
The record links to 0 conditions, and to 1 intervention - of which BOS172738 is the first listed.
NCT03780517 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03780517 about?
NCT03780517 is a clinical study titled "Safety, Efficacy, and Tolerability of BOS172738 in Patients With Advanced Rearranged During Transfection (RET) Gene-Altered Tumors". This study will be conducted to assess the safety and tolerability of BOS172738 when administered to patients with advanced solid tumors with rearranged during transfection (RET) gene alterations and also to establish the maximum tolerated dose (MTD) and/or recommended phase 2 dose (RP2D) of BOS1727...
What is the current status of trial NCT03780517?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 117 participants. The study started on 2018-12-12. Estimated completion is 2023-09-26.
What interventions are being tested in trial NCT03780517?
The interventions under investigation include: BOS172738 (DRUG).
Who is sponsoring clinical trial NCT03780517?
This trial is sponsored by Boston Pharmaceuticals, which has 6 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03780517's enrollment target sits among peer trials
117 499th of 2000 higher than 1,500 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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