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| Sponsored by: |
Daiichi Pharmaceuticals |
| Information provided by: | NIH AIDS Clinical Trials Information Service |
| ClinicalTrials.gov Identifier: | NCT00002342 |
Purpose
To evaluate the safety of different doses and dosing regimens of tecogalan sodium (DS-4152) and to establish the MTD at each of the different dosing schedules.
| Condition | Intervention | Phase |
|
Sarcoma, Kaposi HIV Infections |
Drug: Tecogalan sodium |
Phase I |
| MedlinePlus related topics: | AIDS Cancer Kaposi's Sarcoma Soft Tissue Sarcoma |
| Drug Information available for: | Tecogalan |
| Study Type: | Interventional |
| Study Design: | Treatment, Dose Comparison, Safety Study |
| Official Title: | A Phase I Trial of Tecogalan Sodium (DS-4152) Administered as an Infusion Twice Weekly for 21 Days |
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Patients must have:
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
Concurrent Medication:
Excluded:
Patients with the following prior conditions are excluded:
Prior Medication:
Excluded:
Contacts and Locations
More Information
| Study ID Numbers: | 088C, 4152A-PRT004 |
| First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00002342 |
| Health Authority: | United States: Food and Drug Administration |
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