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NCT06155500 · ClinicalTrials.gov registry record · Phase 1
Long-term Follow-up (LTFU) of Patients Treated With Genome-edited Autologous Hematopoietic Stem and Progenitor Cells (HSPC)
A Phase 1 study of Sickle Cell Disease, sponsored by Novartis Pharmaceuticals.
- Active
- Registry status
- Phase 1
- Development phase
- 4
- Enrollment target
- 3
- Study locations
NCT06155500 is a Phase 1 study of Sickle Cell Disease that is active but no longer recruiting, run by Novartis Pharmaceuticals. The registered enrollment target is 4 participants, below the 293-participant average among 213 other Sickle Cell Disease trials with a reported enrollment target (99% lower). The trial reports 3 study locations across 3 states.
The verdict
NCT06155500, a Phase 1 study of Sickle Cell Disease, is active but no longer recruiting, sponsored by Novartis Pharmaceuticals.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 1
- Development phase
- 4 participants
- Enrollment target
- 3
- Study locations
Study Summary
CADPT03A12001 is a prospective, multi-center study that is designed to follow all enrolled patients who have received treatment with OTQ923 for long-term safety and efficacy.
Conditions Studied
Interventions
- BIOLOGICAL OTQ923
Study Locations (3)
Illinois
- University of Chicago - Chicago
New York
- Memorial Sloan Kettering Cancer Ctr - New York
Tennessee
- St Jude Childrens Research Hospital - Memphis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 4 participants |
| Start Date | 2024-04-16 |
| Est. Completion | 2039-01-11 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06155500
The ClinicalTrials.gov registry entry for NCT06155500 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 293-participant average among 213 other Sickle Cell Disease trials with a reported enrollment target (99% lower). The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Sickle Cell Disease appearing as the primary indexed condition, and to 1 intervention - of which OTQ923 is the first listed.
NCT06155500 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Illinois, New York, Tennessee.
Frequently Asked Questions
What is clinical trial NCT06155500 about?
NCT06155500 is a clinical study titled "Long-term Follow-up (LTFU) of Patients Treated With Genome-edited Autologous Hematopoietic Stem and Progenitor Cells (HSPC)". CADPT03A12001 is a prospective, multi-center study that is designed to follow all enrolled patients who have received treatment with OTQ923 for long-term safety and efficacy.
What is the current status of trial NCT06155500?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 4 participants. The study started on 2024-04-16. Estimated completion is 2039-01-11.
What conditions does trial NCT06155500 study?
This clinical trial studies the following conditions: Sickle Cell Disease.
What interventions are being tested in trial NCT06155500?
The interventions under investigation include: OTQ923 (BIOLOGICAL).
Who is sponsoring clinical trial NCT06155500?
This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06155500 being conducted?
This trial has 3 study locations across Illinois, New York, Tennessee. 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
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.