Trial of Anti-PSMA Designer T Cells in Advanced Prostate Cancer After Non-Myeloablative Conditioning
Phase Ia/Ib Trial of Anti-PSMA Designer T Cells in Prostate Cancer After Non-Myeloablative Conditioning
調査の概要
研究の種類
入学 (予想される)
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究場所
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Rhode Island
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Providence、Rhode Island、アメリカ、02908
- Roger Williams Medical Center
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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:
5.2.1 Patient with histologically confirmed diagnosis of prostate cancer.
5.2.2 Patient with rising serum PSA,(prostate specific antigen).
5.2.3 Tumor is hormone refractory, as documented by rising PSA with two values separated in time. Patients may enroll if they have a rising PSA after withdrawal of androgen therapy but if enrolled onto this protocol on androgen ablation therapy, they must remain on the androgen therapy for the duration of this protocol. Patients may enroll if tumor is not hormone refractory only if they refuse hormone therapy at this time, and that they understand that hormone therapy is standard treatment for their disease at this stage.
5.2.4 Patient must be at least 18 years of age.
5.2.5 Patient able to understand and sign informed consent.
5.2.6 Patient with a life expectancy of greater than four months.
5.2.7 Patient with performance status of 0 to 1. (http://www.ecog.org/general/perf_stat.html).
5.2.8 Patient with adequate organ function as defined by:
5.2.8.1 ANC 1.0, platelets 50,000, Hgb 8.0; patient may be transfused to achieve Hgb 8.0 to satisfy enrollment criteria, or as otherwise indicated by symptoms for Hgb >8.0.
5.2.8.2 Creatinine 1.5mg/dl or creatinine clearance 60cc/min.
5.2.8.3 Direct bilirubin 1.5 mg/dl.
5.2.8.4 No evidence of congestive heart failure, symptoms of coronary artery disease, serious cardiac arrhythmias, including atrial fibrillation/atrial flutter, evidence of prior myocardial infarction by history or EKG. A normal cardiac stress test for inducible ischemia or arrhythmia within 12 weeks prior to enrollment for all patients over 50 years old or those with abnormal EKG or any history or symptoms suggestive of cardiac disease.
5.2.8.5 No serious, symptomatic obstructive or emphysema¬tous lung disease, or asthma requiring intravenous medications within the past 12 months; no serious lung disease associated with dyspnea at normal activity levels (grade III) or at rest (grade IV), due to any cause (including cancer metastases and pleural effusions). The patient will be ineligible if PFTs show an FEV1 <1.3 liters or a DLCO <50% within 12 weeks of study entry.
For patients enrolling in cohorts IIA, IIB, and III:
5.2.9 Patients with disease in the bone or other site(s) have biopsy-able tumor (at radiologically- or externally-accessible site), and willing to undergo biopsy as specified in 6.3.6. For these groups, patients with >5 lesions bone scan positive lesions will be preferred to increase the yield of blind bone marrow biopsies.
Alternatively, patients with bone or extra-skeletal lesions may be biopsied by CT guided or open procedure.
Exclusion Criteria:
5.3.1 Patients with serious or unstable renal, hepatic, pulmonary, cardiovascular, endocrine, rheumatologic, or allergic disease based on history, physical exam and laboratory tests will be excluded, as outlined in section 5.2.9.
5.3.2 Patients with active clinical disease caused by CMV, hepatitis B or C, HIV or tuberculosis will be excluded from the study.
5.3.3 Patients who have had cytotoxic and/or radiation therapy in the four weeks prior to entry or who have initiated anti-androgen therapy less than six weeks prior to entry will be excluded.
5.3.4 Patients with other concurrent malignancies will be excluded.
5.3.5 Patients requiring systemic steroids will be excluded.
5.3.6 Patients with prior investigational therapies within the 4 weeks prior to entry will be excluded.
5.3.7 Patients previously exposed to mouse antibody will be excluded, unless proven by ELISA to have a negative baseline human anti-mouse antibody (HAMA) titer.
5.3.8 Patients who have had irradiation to whole pelvis or to more than 25% of total marrow will be excluded.
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
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- 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 |
|---|---|
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実験的:Anti PSMA Designer T Cells
Open Label, subjects receive anti PSMA designer T cells, plus IL2, low or moderate dose.
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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 |
時間枠 |
|---|---|
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有害事象のある参加者の数
時間枠:30日
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30日
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協力者と研究者
研究記録日
主要日程の研究
研究開始
一次修了 (予想される)
研究の完了 (予想される)
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
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
Anti-PSMA Designer T Cellsの臨床試験
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Cancer Institute and Hospital, Chinese Academy...募集
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Cancer Institute and Hospital, Chinese Academy...募集
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Ankara UniversityOncosia Scientific GmbH; EDH Nukleer Tip ve Saglik Hizmetleri Ltd. Sti.まだ募集していません
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Shenzhen Geno-Immune Medical InstituteThe Seventh Affiliated Hospital of Sun Yat-sen University; Shenzhen Children's Hospital; Shenzhen...募集
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Shanghai Changzheng HospitalBioray Laboratories積極的、募集していない
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Fusion Pharmaceuticals Inc.積極的、募集していない
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Nanjing First Hospital, Nanjing Medical Universityわからない
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Peter MacCallum Cancer Centre, Australia積極的、募集していない前立腺がん | 転移性去勢抵抗性前立腺がん | MCRPCオーストラリア