Phase I Study of Safety, Tolerability, and Pharmacokinetics of Viracept in HIV-1 Infected Children and Exposed Infants
調査の概要
詳細な説明
This is a study of the safety, tolerability and pharmacokinetics of a Viracept pediatric powder formulation with milk or formula. First a single dose will be administered. After the patient population is divided into 4 groups by age, an optimal dose will be determined for each group. This optimal dose will be given 3 times a day for a 6 week primary observation period, plus an optional 6 month extension.
NOTE: During the single dose portion of this study, patients may be untreated or may continue treatment with their current nucleoside antiretroviral therapy. During multiple dose administration of Viracept, antiretroviral therapy will be intensified by either adding or modifying therapy. Antiretroviral therapies will be limited to those currently licensed including zidovudine, lamivudine, stavudine, didanosine or zalcitabine.
研究の種類
入学
段階
- フェーズ 1
連絡先と場所
研究場所
-
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California
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Los Angeles、California、アメリカ、90024
- UCLA School of Medicine / Dept of Pediatrics
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria
Concurrent Medication:
Allowed:
Administration of Pneumocystis carinii pneumonia prophylaxis according to CDC guidelines will be permitted.
Patients must have:
- For children >= 3 months to 13 years of age:
- HIV infection. For children <3 months of age:
- HIV infection or exposure.
- Newborns must have birth weight >= 2500 gm.
- Absence at screen of any serious or unstable medical conditions.
- Parent or guardian able to give written informed consent and willing to comply with study requirements.
Exclusion Criteria
Co-existing Condition:
Patients with any of the following symptoms or conditions are excluded:
- Children with HIV associated malignancy requiring chemotherapy.
- Children with clinical or laboratory assessments greater than Grade 1 in the Toxicity Table at the time of the screening.
Concurrent Medication:
Excluded:
Chemotherapy.
Prior Medication:
Excluded:
- Protease inhibitors.
NOTE:
- Patients who have taken investigational agents, immunomodulators, HIV-1 vaccines, glucocorticoids or unconventional therapies within one month prior to the day 0 of the study must be evaluated to determine the impact of these treatments on the study. Patients may be included or excluded on a case to case basis.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
協力者と研究者
スポンサー
研究記録日
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- 259E
- AG 1343-524
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