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NCT02252263 · ClinicalTrials.gov registry record · Phase 1
A Phase I Open Label Study of the Safety and Tolerability of Elotuzumab (BMS-901608) Administered in Combination With Either Lirilumab (BMS-986015) or Urelumab (BMS-663513) in Subjects With Multiple Myeloma
A Phase 1 study of Multiple Myeloma, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 44
- Enrollment target
- 7
- Study locations
NCT02252263 is a Phase 1 study of Multiple Myeloma that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 44 participants, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (92% lower). The trial reports 7 study locations across 7 states.
The verdict
NCT02252263, a Phase 1 study of Multiple Myeloma, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 44 participants
- Enrollment target
- 7
- Study locations
Study Summary
To assess the safety and tolerability, characterize the dose limiting toxicities (DLTs) and identify the maximally tolerated dose (MTD) of Elotuzumab administered in combination with either Lirilumab or Urelumab in subjects with multiple myeloma.
Conditions Studied
Interventions
- DRUG Elotuzumab
- DRUG Urelumab
- DRUG Lirilumab
Study Locations (7)
Arkansas
- University Of Arkansas For Medical Sciences - Little Rock
Maryland
- The Sidney Kimmel Comprehensive Cancer Center - Baltimore
New York
- Memorial Sloan Kettering Cancer Center - New York
Ohio
- The Ohio State University - Columbus
Oregon
- Oregon Health & Science University - Portland
Pennsylvania
- University Of Pennsylvania - Philadelphia
Navarre
- Local Institution - Pamplona
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2014-12-09 |
| Est. Completion | 2017-10-10 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02252263
The ClinicalTrials.gov registry entry for NCT02252263 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (92% lower). The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Multiple Myeloma appearing as the primary indexed condition, and to 3 interventions - of which Elotuzumab is the first listed.
NCT02252263 reports 7 study locations spanning 7 distinct geographic areas - top geographies include Arkansas, Maryland, New York.
Frequently Asked Questions
What is clinical trial NCT02252263 about?
NCT02252263 is a clinical study titled "A Phase I Open Label Study of the Safety and Tolerability of Elotuzumab (BMS-901608) Administered in Combination With Either Lirilumab (BMS-986015) or Urelumab (BMS-663513) in Subjects With Multiple Myeloma". To assess the safety and tolerability, characterize the dose limiting toxicities (DLTs) and identify the maximally tolerated dose (MTD) of Elotuzumab administered in combination with either Lirilumab or Urelumab in subjects with multiple myeloma.
What is the current status of trial NCT02252263?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2014-12-09. Estimated completion is 2017-10-10.
What conditions does trial NCT02252263 study?
This clinical trial studies the following conditions: Multiple Myeloma.
What interventions are being tested in trial NCT02252263?
The interventions under investigation include: Elotuzumab (DRUG), Urelumab (DRUG), Lirilumab (DRUG).
Who is sponsoring clinical trial NCT02252263?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02252263 being conducted?
This trial has 7 study locations across Arkansas, Maryland, New York, Ohio, Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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