Topical Use of 4,4'-Dihydroxybenzophenone-2,4-Dinitrophenylhydrazone (A-007) in the Treatment of Advanced Malignancies Including Kaposi's Sarcoma and Lymphoproliferative Disorders
This study has been completed.
Sponsor:
DEKK-TEC, Inc.
Information provided by:
NIH AIDS Clinical Trials Information Service
ClinicalTrials.gov Identifier:
NCT00002153
First received: November 2, 1999
Last updated: June 23, 2005
Last verified: May 1999
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Purpose
To evaluate topical A-007 in patients with advanced malignancies including Kaposi's sarcoma and lymphoproliferative disorders.
| Condition | Intervention | Phase |
|---|---|---|
|
Sarcoma, Kaposi HIV Infections Lymphoproliferative Disorders |
Drug: A-007 |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Primary Purpose: Treatment |
| Official Title: | Topical Use of 4,4'-Dihydroxybenzophenone-2,4-Dinitrophenylhydrazone (A-007) in the Treatment of Advanced Malignancies Including Kaposi's Sarcoma and Lymphoproliferative Disorders |
Resource links provided by NLM:
Further study details as provided by NIH AIDS Clinical Trials Information Service:
Eligibility| Ages Eligible for Study: | 21 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria
Concurrent Medication:
Allowed:
- Maintenance antihormones, hormones, and glucocorticoids.
Patients must have:
- Histologically proven metastatic cancer including Kaposi's sarcoma and lymphoproliferative disorders to the skin or cutaneous sites. NOTE:
- Primary basal or squamous cell cancer of the skin is allowed.
- Failed both primary and secondary chemotherapy and/or immunotherapy protocols.
- Measurable skin or cutaneous lesions. 4 Life expectancy of at least 20 weeks.
Prior Medication:
Required:
- Prior therapy for cutaneous lesions from Kaposi's sarcoma or lymphoproliferative disorders.
Allowed:
- Prior maintenance steroids and hormone/antihormone therapy.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Active infections other than medically stable HIV infection.
- Active congestive heart failure, any persistent arrhythmia or transient serious arrhythmia (ventricular tachycardia, sinoatrial arrest, etc.), or progressive cardiomyopathy.
- Unstable blood pressure.
- Seizures or other CNS disorders.
- Severe unstable diabetes mellitus.
- Coagulopathies.
- Thrombotic disease.
- Any other medical conditions that would prevent completion of study or produce significant risk to patient.
Concurrent Medication:
Excluded:
- Concomitant chemotherapy or immunotherapy.
- Ongoing corticosteroid therapy (unless maintenance).
Patients with the following prior conditions are excluded:
- History of active cardiopulmonary or respiratory disease.
- History of sun hypersensitivity and photosensitive dermatoses.
- History of allergy or hypersensitivity to cosmetics, toiletries, or other dermatological products.
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00002153 History of Changes |
| Other Study ID Numbers: | 247A, DTI-006 |
| Study First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by NIH AIDS Clinical Trials Information Service:
|
Skin Neoplasms Sarcoma, Kaposi Acquired Immunodeficiency Syndrome Antineoplastic Agents |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lymphoproliferative Disorders Sarcoma, Kaposi Sarcoma Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases |
Slow Virus Diseases Lymphatic Diseases Immunoproliferative Disorders Herpesviridae Infections DNA Virus Infections Neoplasms, Connective and Soft Tissue Neoplasms by Histologic Type Neoplasms Neoplasms, Vascular Tissue Antineoplastic Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 16, 2013