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COMPLETED Phase 1

A Dose-escalation Study of the Safety and Tolerability of Orally Administered TG101348 in Patients With Myelofibrosis

NCT00631462 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the safety and tolerability of orally administered TG101348 in patients with myelofibrosis.

Conditions Studied

Interventions

  • DRUG TG101348

Study Locations (6)

California

  • UCSD Moores Cancer Center — San Diego
  • Stanford Comprehensive Cancer Center — Stanford

Massachusetts

  • Dana Farber Cancer Institute — Boston

Michigan

  • University of Michigan Comprehensive Cancer Center — Ann Arbor

Minnesota

  • Mayo Clinic, Rochester — Rochester

Texas

  • MD Anderson Cancer Center — Houston

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2008-01
Est. Completion 2009-10
Phase Phase 1

Sponsor

TargeGen

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00631462

The ClinicalTrials.gov registry entry for NCT00631462 describes a study currently listed as completed. 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 59 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is TargeGen, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Myelofibrosis appearing as the primary indexed condition, and to 1 intervention — of which TG101348 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: NCT00631462 reports 6 study locations spanning 5 distinct geographic areas — top geographies include California, Massachusetts, Michigan. 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 NCT00631462 about?

NCT00631462 is a clinical study titled "A Dose-escalation Study of the Safety and Tolerability of Orally Administered TG101348 in Patients With Myelofibrosis". The purpose of this study is to evaluate the safety and tolerability of orally administered TG101348 in patients with myelofibrosis.

What is the current status of trial NCT00631462?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 59 participants. The study started on 2008-01. Estimated completion is 2009-10.

What conditions does trial NCT00631462 study?

This clinical trial studies the following conditions: Myelofibrosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00631462?

The interventions under investigation include: TG101348 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00631462?

This trial is sponsored by TargeGen, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00631462 being conducted?

This trial has 6 study locations across California, Massachusetts, Michigan, Minnesota, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial