Fact Sheet:
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| Unique Identifier | FDA/00535 |
| Protocol ID Numbers | FDA 131A |
| Protocol Title | Phase I study to evaluate the safety and tolerance of RMP-7 administered with amphotericin B to patients with HIV infection and cryptococcal meningitis. |
| General Description | To evaluate the safety of escalating doses of RMP-7 administered in persons with HIV infection and cryptococcal meningitis and to determine the MTD of the drug. |
| Open/Closed Indicator | Open: actively accruing patients (930301). |
| Disease Studied | Cryptococcal meningitis. |
| Patient Inclusion Criteria | General Inclusion Criteria: Patients must have: 1. HIV infection. 2. Acute cryptococcal meningitis. |
| Patient Age | Age: 18 - 99 |
| Patient Sex | Male; Female |
| Patient Exclusion Criteria | General Exclusion Criteria: Patients with the following prior conditions are excluded: 1. History of bleeding disorder. 2. History of active renal or hepatic disease... |
| Substance Identification | Drug 1: DRG-0182: RMP-7 Drug 2: DRG-0006: Amphotericin B |
| Location of Trial | Los Angeles County / USC Medical Center 1200 North State Street, Los Angeles, CA 90033; Contact: DeAnn Diamond (213) 226-3695 OPEN 930301... |
| Supporting Agency | Alkermes Incorporated. |
| MESH | Acquired Immunodeficiency Syndrome/complications; Adult; Aged; Amphotericine B/*pharmacokinetics/toxicity;... |
| Entry Month | 9307 |
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