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An Extension Study of Venetoclax for Subjects Who Have Completed a Prior Venetoclax Clinical Trial
NCT03844048 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this extension study is to provide venetoclax and obtain long-term safety data for subjects who continue to tolerate and derive benefit from receiving venetoclax in ongoing studies.
Conditions Studied
Interventions
- DRUG Venetoclax
Study Locations (20)
New South Wales
- Royal Prince Alfred Hospital /ID# 239557 — Camperdown
- St George Hospital /ID# 225589 — Kogarah
- Liverpool Hospital /ID# 225591 — Liverpool
Western Australia
- Fiona Stanley Hospital /ID# 239480 — Murdoch
- Perth Blood Institute Ltd /ID# 225592 — Nedlands
Arizona
- University of Arizona Cancer Center - Tucson /ID# 210548 — Tucson
California
- UCLA Santa Monica Hematology Oncology /ID# 210551 — Los Angeles
Illinois
- Ingalls Memorial Hosp /ID# 210553 — Harvey
Massachusetts
- Dana-Farber Cancer Institute /ID# 215360 — Boston
Michigan
- University of Michigan Comprehensive Cancer Center Michigan Medicine /ID# 231132 — Ann Arbor
New Hampshire
- Dartmouth-Hitchcock Medical Center /ID# 210555 — Lebanon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 165 participants |
| Start Date | 2019-09-06 |
| Est. Completion | 2027-08 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03844048
The ClinicalTrials.gov registry entry for NCT03844048 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 165 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie, which has 603 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 6 conditions, with Cancer appearing as the primary indexed condition, and to 1 intervention — of which Venetoclax is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03844048 reports 20 study locations spanning 17 distinct geographic areas — top geographies include New South Wales, Western Australia, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03844048 about?
NCT03844048 is a clinical study titled "An Extension Study of Venetoclax for Subjects Who Have Completed a Prior Venetoclax Clinical Trial". The purpose of this extension study is to provide venetoclax and obtain long-term safety data for subjects who continue to tolerate and derive benefit from receiving venetoclax in ongoing studies.
What is the current status of trial NCT03844048?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 165 participants. The study started on 2019-09-06. Estimated completion is 2027-08.
What conditions does trial NCT03844048 study?
This clinical trial studies the following conditions: Cancer, Multiple Myeloma, Acute Myeloid Leukemia, Chronic Lymphocytic Leukemia, Acute Lymphoblastic Leukemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03844048?
The interventions under investigation include: Venetoclax (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03844048?
This trial is sponsored by AbbVie, which has 603 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03844048 being conducted?
This trial has 20 study locations across Arizona, California, Illinois, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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