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NCT03672695 · ClinicalTrials.gov registry record · Phase 1
Phase I Dose Escalation Study of Intravenously Administered S64315 in Combination With Orally Administered Venetoclax in Patients With Acute Myeloid Leukaemia.
A Phase 1 study, sponsored by Institut de Recherches Internationales Servier.
- Completed
- Registry status
- Phase 1
- Development phase
- 37
- Enrollment target
NCT03672695: Completed Phase 1 study, sponsored by Institut de Recherches Internationales Servier.
NCT03672695 is a Phase 1 study that has completed, run by Institut de Recherches Internationales Servier. The registered enrollment target is 37 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03672695, a Phase 1 study, has completed, sponsored by Institut de Recherches Internationales Servier.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 37 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the safety profile, tolerability and the Recommended Phase 2 Dose of the combination S64315 with venetoclax in patients with Acute Myeloid Leukaemia.
Interventions
- COMBINATION_PRODUCT S 64315 (also referred as MIK665) and venetoclax
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2018-11-28 |
| Est. Completion | 2023-05-30 |
| Phase | Phase 1 |
What the finished NCT03672695 record still lists
NCT03672695 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% lower).
The record links to 0 conditions, and to 1 intervention - of which S 64315 (also referred as MIK665) and venetoclax is the first listed.
NCT03672695 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03672695 about?
NCT03672695 is a clinical study titled "Phase I Dose Escalation Study of Intravenously Administered S64315 in Combination With Orally Administered Venetoclax in Patients With Acute Myeloid Leukaemia.". The purpose of this study is to determine the safety profile, tolerability and the Recommended Phase 2 Dose of the combination S64315 with venetoclax in patients with Acute Myeloid Leukaemia.
What is the current status of trial NCT03672695?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 37 participants. The study started on 2018-11-28. Estimated completion is 2023-05-30.
What interventions are being tested in trial NCT03672695?
The interventions under investigation include: S 64315 (also referred as MIK665) and venetoclax (COMBINATION_PRODUCT).
Who is sponsoring clinical trial NCT03672695?
This trial is sponsored by Institut de Recherches Internationales Servier, which has 27 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03672695's enrollment target sits among peer trials
37 1204th of 2000 higher than 791 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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