The Effect of Ixazomib on the Latent HIV Reservoir
2021年12月8日 更新者:Nathan W. Cummins, M.D.、Mayo Clinic
Pilot Study of Ixazomib to Reduce the Number of HIV DNA Positive Lymphoid Cells
The primary purpose of the trial is to determine the safety and tolerability of ixazomib in HIV infected patients on antiretroviral therapy.
The secondary purpose is to determine the effect of ixazomib on the size of the HIV reservoir.
調査の概要
研究の種類
介入
入学 (実際)
17
段階
- フェーズ2
- フェーズ 1
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
-
-
Minnesota
-
Rochester、Minnesota、アメリカ、55905
- Mayo Clinic
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
18年歳以上 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- The following laboratory values obtained <=14 days prior to registration.
- ANC ≥ LLN (lower limit of normal) and ≤ULN (upper limit of normal), Hgb ≥ LLN and ≤ULN, PLT ≥ LLN and ≤ULN
- Total bilirubin ≤ULN and the direct bilirubin must be ≤ ULN; AST <1.5 x ULN and ALT <1.5 x ULN
- Creatinine <2.0 x ULN and an estimated creatinine clearance > 60 ml/min
- HIV infection with suppressed viral replication on at least 3 active drug ART for at least 6 months
- Suppressed viral replication is defined by plasma HIV viral load <20copies/mL.
- Patient must have HIV viral load <20 copies/ml on two occasions at least 3 months apart.
- In the opinion of the treating physician, patients must have available other regimens likely to suppress HIV should their current regimen fail.
- Male or female patients age >=18 years
- A plasma HIV RNA viral load demonstrating a measure of <20 copies/mL within 30 days prior to study initiation.
- CD4 count >500 cells/mm3 within 30 days prior to study enrollment
- Females must have a negative pregnancy test prior to receiving the 1st dose of ixazomib and be postmenopausal for at least 1 year before the screen visit, or surgically sterile,
Male patients, even if surgically sterilized (ie, status post-vasectomy), must agree to one of the following:
- Agree to practice effective barrier contraception AND a second method of contraception for female partners of childbearing potential during the entire study treatment period and through 90 days after the last dose of ixazomib,
- OR
- Agree to practice true abstinence when this is in line with the preferred and usual lifestyle of the subject. (Periodic abstinence (eg, calendar, ovulation, symptothermal, post-ovulation methods] and withdrawal are not acceptable methods of contraception.)
- AND
- Agree to forego sperm donation for the same period as above.
Exclusion Criteria:
The following laboratory values obtained <=14 days prior to registration.
- ANC < LLN and >ULN, Hgb < LLN and >ULN, PLT < LLN and >ULN
- Total bilirubin >ULN or the direct bilirubin is > ULN; AST >1.5 x ULN or AST >1.5 x ULN
- Creatinine >=2.0 x ULN or an estimated creatinine clearance <=60mL/min
- Diagnosed and treated for a malignancy within 5 years before randomization, or previously diagnosed with a malignancy and have any evidence of residual disease. Patients with nonmelanoma skin cancer or carcinoma in situ of any type are not excluded if they have undergone complete resection
- Any infection except HIV (excluding benign conditions that is unlikely to be affected or modulated by treatment with ixazomib, e.g. stye or furuncle), or treatment with anti-infective agents within 14 days of enrollment.
- Pregnant women
- Women of childbearing potential and Nursing women
- Men who are unwilling to use a condom (even if they have undergone a prior vasectomy) while having intercourse, while taking the drug and for 90 days after stopping ixazomib.
- Any history of peripheral neuropathy, or peripheral neuropathy detected during the screening period.
- Major surgery within 14 days before study registration
- Systemic treatment with strong CYP3A inducers (rifampin, rifapentine, rifabutin,carbamazepine, phenytoin, phenobarbital), or use of St. John's wort.
- Evidence of current uncontrolled cardiovascular conditions, including serious cardiac arrhythmias, congestive heart failure, angina, or myocardial infarction within the past 6 months.
- QTc > 450 milliseconds (msec) for men and >470 milliseconds for women (83) on a 12 lead ECG obtained during the Screening period.
- Known hepatitis B DNA positive status and/or HBsAg positive and/or HBeAg positive, or active hepatitis C replication (HCV RNA positive) or currently on hepatitis C treatment.
- Known history of cirrhosis or active liver inflammation, including "fatty liver" or non-alcohol steatohepatitis (NASH).
- Any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of treatment according to this protocol.
- Known allergy to any of the study medications, their analogues or excipients in the various formulations.
- Any other recent or concurrent medical condition that, in the Investigator's opinion, would impose any risk to the patient
- Known GI disease or GI procedure that could interfere with the oral absorption or tolerance of ixazomib including difficulty swallowing.
- Participation in other clinical trials, including those with other investigational agents not included in this trial, within 30 days of the start of this trial and throughout the duration of this trial.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
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
- 割り当て:非ランダム化
- 介入モデル:順次割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Ixazomib 1 mg
Cohort A: Patients will receive ixazomib 1mg 3 times monthly for 12 weeks, then weekly for 12 weeks.
|
1 mg on days 1, 8 and 15 for three 28 days cycles, then be reviewed by DSMB and based upon their recommendation patients will receive ixazomib once weekly for 12 weeks or ixazomib 1 mg on days 1, 8 and 15 for three 28 days cycles.
Visits 3-15 will have a window of ± 3 days.
他の名前:
|
|
実験的:Ixazomib 2 mg
Cohort B: Patients will receive ixazomib 2mg 3 times monthly for 12 weeks, then weekly for 12 weeks.
|
2mg on days 1, 8 and 15 for three 28 days cycles, then be reviewed by DSMB and based upon their recommendation patients will receive ixazomib once weekly for 12 weeks or ixazomib 2 mg on days 1, 8 and 15 for three 28 days cycles.
Visits 3-15 will have a window of ± 3 days.
他の名前:
|
|
実験的:Ixazomib 3 mg
Cohort C: Patients will receive ixazomib 3 mg 3 times monthly for 12 weeks, then weekly for 12 weeks.
|
3 mg on days 1, 8 and 15 for three 28 days cycles, then be reviewed by DSMB and based upon their recommendation patients will receive ixazomib once weekly for 12 weeks or ixazomib 3 mg on days 1, 8 and 15 for three 28 days cycles.
Visits 3-15 will have a window of ± 3 days.
他の名前:
|
|
実験的:Ixazomib 4 mg
Cohort D: Patients will receive ixazomib 4mg 3 times monthly for 12 weeks, then weekly for 12 weeks.
|
4 mg on days 1, 8 and 15 for three 28 days cycles, then be reviewed by DSMB and based upon their recommendation patients will receive ixazomib once weekly for 12 weeks or ixazomib 4 mg on days 1, 8 and 15 for three 28 days cycles.
Visits 3-15 will have a window of ± 3 days.
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Incidence of Treatment-Emergent Adverse Events
時間枠:7 months
|
Number of treatment-emergent adverse events experienced by subjects as defined by NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.0
|
7 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Cell Associated HIV DNA in CD4 T Cell Subsets
時間枠:24 weeks
|
HIV copies per million CD4 T cells
|
24 weeks
|
|
Culturable HIV by Quantitative Viral Outgrowth Assay
時間枠:24 weeks
|
Infectious units per million CD4 T cells
|
24 weeks
|
|
Absolute CD4 T Cell Count
時間枠:24 weeks
|
Cells per microliter
|
24 weeks
|
|
Absolute CD8 T Cell Count
時間枠:24 weeks
|
Cells per microliter
|
24 weeks
|
|
CD4/CD8 Ratio
時間枠:24 weeks
|
CD4/CD8 T cell count ratio
|
24 weeks
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
便利なリンク
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2017年3月20日
一次修了 (実際)
2019年8月19日
研究の完了 (実際)
2019年8月19日
試験登録日
最初に提出
2016年10月24日
QC基準を満たした最初の提出物
2016年10月25日
最初の投稿 (見積もり)
2016年10月26日
学習記録の更新
投稿された最後の更新 (実際)
2022年1月6日
QC基準を満たした最後の更新が送信されました
2021年12月8日
最終確認日
2021年12月1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
- 16-001938
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
はい
米国FDA規制機器製品の研究
いいえ
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