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A Study of Targretin Capsules in Patients With AIDS-Related Kaposi's Sarcoma
NCT00002212 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to see if it is safe and effective to give Targretin capsules to patients with AIDS-related Kaposi's sarcoma (KS).
Conditions Studied
Interventions
- DRUG Bexarotene
Study Locations (3)
California
- Desert Univ School of Medicine — Palm Springs
Louisiana
- Tulane Univ School of Medicine — New Orleans
Pennsylvania
- Milton S Hershey Med Ctr — Hershey
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 27 participants |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00002212
The ClinicalTrials.gov registry entry for NCT00002212 describes a study currently listed as completed. It is categorized as Phase 2, 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 27 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ligand Pharmaceuticals, 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 2 conditions, with HIV Infections appearing as the primary indexed condition, and to 1 intervention — of which Bexarotene 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: NCT00002212 reports 3 study locations spanning 3 distinct geographic areas — top geographies include California, Louisiana, Pennsylvania. 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 NCT00002212 about?
NCT00002212 is a clinical study titled "A Study of Targretin Capsules in Patients With AIDS-Related Kaposi's Sarcoma". The purpose of this study is to see if it is safe and effective to give Targretin capsules to patients with AIDS-related Kaposi's sarcoma (KS).
What is the current status of trial NCT00002212?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 27 participants.
What conditions does trial NCT00002212 study?
This clinical trial studies the following conditions: HIV Infections, Sarcoma, Kaposi. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00002212?
The interventions under investigation include: Bexarotene (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00002212?
This trial is sponsored by Ligand Pharmaceuticals, 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 NCT00002212 being conducted?
This trial has 3 study locations across California, Louisiana, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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