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A Study to Assess the Safety, Tolerability, and Efficacy of NDI-219216 in Patients With Advanced Solid Tumors.
NCT06898450 · View on ClinicalTrials.gov ↗
Study Summary
The goal of this clinical trial is to learn if NDI-219216 is safe for patients, and if NDI-219216 might be a possible treatment for advanced solid tumors in the later phases of the study. The main questions it aims to answer are: Is NDI-219216 safe and what kinds of side effects might it cause? What kind of effects does NDI-219216 have on the body? Does NDI-219216 have any impact on tumor size? Participants will: Take NDI-219216 every day by mouth. Visit the clinic 6 times during Cycle 1, 2 times during Cycle 2, once a month thereafter for checkups and tests while on the study, then one time for an end of treatment visit. After the End of Study, a follow up will occur but can be done on the phone. Keep a diary of their tablet consumption and symptoms experienced.
Conditions Studied
Interventions
- DRUG NDI-219216
Study Locations (20)
Other
- Hôpital Saint-Antoine - Assistance Publique-Hopitaux de Paris (AP-HP) — Paris
- Centre Hospitalier Universitaire (CHU) de Poitiers — Poitiers
- START Dublin — Dublin
- START Lisbon — Lisbon
North Carolina
- Levine Cancer Center — Charlotte
- Atrium Health Wake Forest Baptist Center — Winston-Salem
Virginia
- University of Virginia Emily Couric Clinical Cancer Center — Charlottesville
- Virginia Cancer Specialists, P.C. - Fairfax — Fairfax
California
- USC Norris Comprehensive Cancer Center — Los Angeles
Illinois
- University of Chicago Medicine — Chicago
Kentucky
- University of Louisville James Graham Brown Cancer Center — Louisville
New York
- Cayuga Cancer Center — Ithaca
Ohio
- Taylor Cancer Research Center — Maumee
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 134 participants |
| Start Date | 2025-03-31 |
| Est. Completion | 2031-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06898450
The ClinicalTrials.gov registry entry for NCT06898450 describes a study currently listed as recruiting. It is categorized as Phase 1, 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 134 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Nimbus Wadjet, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Advanced Solid Tumors Cancer appearing as the primary indexed condition, and to 1 intervention — of which NDI-219216 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: NCT06898450 reports 20 study locations spanning 15 distinct geographic areas — top geographies include Other, North Carolina, Virginia. 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 NCT06898450 about?
NCT06898450 is a clinical study titled "A Study to Assess the Safety, Tolerability, and Efficacy of NDI-219216 in Patients With Advanced Solid Tumors.". The goal of this clinical trial is to learn if NDI-219216 is safe for patients, and if NDI-219216 might be a possible treatment for advanced solid tumors in the later phases of the study. The main questions it aims to answer are: Is NDI-219216 safe and what kinds of side effects might it cause? Wh...
What is the current status of trial NCT06898450?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 134 participants. The study started on 2025-03-31. Estimated completion is 2031-12.
What conditions does trial NCT06898450 study?
This clinical trial studies the following conditions: Advanced Solid Tumors Cancer, MSI-H Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06898450?
The interventions under investigation include: NDI-219216 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06898450?
This trial is sponsored by Nimbus Wadjet, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06898450 being conducted?
This trial has 20 study locations across California, Illinois, Kentucky, New York, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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