A Study of ALRT1057 in Patients With AIDS-Related Kaposi's Sarcoma
NCT ID: NCT00002188
Last Updated: 2005-06-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
27 participants
INTERVENTIONAL
Brief Summary
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Detailed Description
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Thirteen patients are treated initially. If at least one response is observed in these patients, up to 14 additional patients will be evaluated.
Conditions
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Study Design
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TREATMENT
Interventions
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Alitretinoin
Eligibility Criteria
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Inclusion Criteria
* HIV positive status and histologic confirmation of KS.
* CD4 count \> 200 mm3 (required of one-half of patients).
* Minimum of 6 mucocutaneous KS lesions, including at least 3 raised lesions meeting criteria for "indicator" lesions.
* Acceptable organ system function.
Exclusion Criteria
Patients with the following conditions or symptoms are excluded:
Serious or intercurrent illness or infection that would interfere with the ability of the patient to carry out the treatment program.
Prior Medication:
Excluded:
* Systemic therapy for KS within 30 days.
* Local or topical therapy for KS indicative lesions within 60 days.
* Systemic therapy with vitamin A in doses exceeding 15,000 IU per day or other retinoid class drug.
Required:
Approved antiretroviral therapy.
18 Years
ALL
No
Sponsors
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Ligand Pharmaceuticals
INDUSTRY
Anderson Clinical Research
INDUSTRY
Other Identifiers
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L1057-28
Identifier Type: -
Identifier Source: secondary_id
96ACR-LIG2
Identifier Type: -
Identifier Source: secondary_id
271A
Identifier Type: -
Identifier Source: org_study_id