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Safety and Anti-leukemic Activity of Vodobatinib (K0706) for Treatment of Ph+ CML Resistant/Intolerant to ≥3 Prior CML Therapies
NCT02629692 · View on ClinicalTrials.gov ↗
Study Summary
Phase 1/2 study to determine safety, tolerability, pharmacokinetics, and anti-leukemic activity of Vodobatinib (K0706) in treatment-refractory/intolerant CML
Conditions Studied
Interventions
- DRUG Vodobatinib (K0706) capsules
Study Locations (20)
Maharashtra
- Prince Aly Khan Hospital — Mumbai
- Tata Memorial Hospital — Mumbai
- Sahyadri Specialty Hospital — Pune
California
- The Oncology Institute of Hope and Innovation, Innovative Clinical Research Institute — Downey
- UCLA Hematologic Malignancy Program — Los Angeles
Texas
- Baylor University Medical Center — Dallas
- MD Anderson Cancer Center — Houston
Other
- Cliniques Universitaires Saint-Luc — Brussels
- Debreceni Egyetem — Debrecen
Rhone
- Centre Léon Bérard — Lyon
- Centre Hospitalier Lyon Sud — Pierre-Bénite
Florida
- Mayo Clinic — Jacksonville
Georgia
- Board of Regents of the University System of Georgia — Augusta
New York
- Memorial Sloan Kettering Cancer Center - MAIN — New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 122 participants |
| Start Date | 2016-06-27 |
| Est. Completion | 2026-08 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02629692
The ClinicalTrials.gov registry entry for NCT02629692 describes a study currently listed as active not 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 122 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sun Pharma Advanced Research Company Limited, which has 7 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 Healthy (For Part A) appearing as the primary indexed condition, and to 1 intervention — of which Vodobatinib (K0706) capsules 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: NCT02629692 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Maharashtra, California, Texas. 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 NCT02629692 about?
NCT02629692 is a clinical study titled "Safety and Anti-leukemic Activity of Vodobatinib (K0706) for Treatment of Ph+ CML Resistant/Intolerant to ≥3 Prior CML Therapies". Phase 1/2 study to determine safety, tolerability, pharmacokinetics, and anti-leukemic activity of Vodobatinib (K0706) in treatment-refractory/intolerant CML
What is the current status of trial NCT02629692?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 122 participants. The study started on 2016-06-27. Estimated completion is 2026-08.
What conditions does trial NCT02629692 study?
This clinical trial studies the following conditions: Healthy (For Part A), Chronic Myeloid Leukemia (for Part B and C). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02629692?
The interventions under investigation include: Vodobatinib (K0706) capsules (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02629692?
This trial is sponsored by Sun Pharma Advanced Research Company Limited, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02629692 being conducted?
This trial has 20 study locations across California, Florida, Georgia, New York, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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