Study of AMG 386 in Combination With Paclitaxel and Carboplatin in Subjects With Ovarian Cancer
2015年10月13日 更新者:Amgen
A Phase 1b Open-Label, Multi-Center Study of AMG 386 in Combination With Paclitaxel and Carboplatin in Subjects With High-Risk Stage I and Stages II-IV Epithelial Ovarian, Primary Peritoneal or Fallopian Tube Cancers
To evaluate whether AMG 386 in combination with paclitaxel and carboplatin is safe and well tolerated in the first-line treatment of high-risk stage I and stages II-IV epithelial ovarian, primary peritoneal and fallopian tube cancers.
The hypothesis is that AMG 386 in combination with carboplatin and paclitaxel is safe and well tolerated.
調査の概要
詳細な説明
To evaluate whether AMG 386 in combination with paclitaxel and carboplatin is safe and well tolerated in the first-line treatment of high-risk stage I and stages II-IV epithelial ovarian, primary peritoneal and fallopian tube cancers.
The hypothesis is that AMG 386 in combination with carboplatin and paclitaxel is safe and well tolerated.
研究の種類
介入
入学 (実際)
27
段階
- 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
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Victoria
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Footscray、Victoria、オーストラリア、3011
- Research Site
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Malvern、Victoria、オーストラリア、3144
- Research Site
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Parkville、Victoria、オーストラリア、3052
- Research Site
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Madrid、スペイン、28040
- Research Site
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Cataluña
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Barcelona、Cataluña、スペイン、08035
- Research Site
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Brussels、ベルギー、1000
- Research Site
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Bruxelles、ベルギー、1200
- Research Site
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Leuven、ベルギー、3000
- Research Site
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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
女性
説明
Inclusion Criteria:
- Female subjects more than 18 years of age with newly diagnosed high-risk FIGO Stage I (grade 3, or aneuploid grade 1 or 2) or Stages II-IV epithelial ovarian, primary peritoneal and fallopian tube cancer with an indication for first-line treatment with paclitaxel and carboplatin x 6 cycles. Subjects with pseudomyxoma, mesothelioma, adenocarcinoma of unknown primary tumor, sarcoma, or neuroendocrine histology are excluded.
- Subjects with high-risk stage I, stage II, or stage IIIA-B must have had prior primary debulking surgery that occurred no less than 4 weeks, and no more than 12 weeks, prior to enrollment. Subjects must have recovered fully from surgery in the opinion of the investigator
- Subjects with Stage IIIC or IV disease who have not had primary debulking surgery must have planned interval debulking surgery following 3 cycles of AMG 386, paclitaxel and carboplatin
- Female 18 years of age or older at the time the written informed consent is obtained
- Subjects of child-bearing potential who have not undergone a bilateral salpingo-oophorectomy and are sexually active must consent to use an accepted and effective non-hormonal method of contraception (i.e, double barrier method (eg, condom plus diaphragm) from signing the informed consent through 6 months after last dose of study drug
- GOG Performance Status of 0 or 1
- Life expectancy ≥ 3 months (per investigator opinion)
- Subject plans to begin protocol-directed therapy within 7 days from enrollment
- Adequate organ and hematological function as evidenced by the following laboratory studies prior to enrollment:
Hematological function, as follows:
- Hemoglobin ≥ 9 g/dL
- Absolute neutrophil count (ANC) ≥ 1.5 x 10x9/L
- Platelet count ≥ 100 x 10x9/L and ≤ 850 x 10x9/L
- PTT or aPTT ≤ 1.5 x ULN per institutional laboratory range and INR ≤ 1.5
Renal function, as follows:
- Urinary protein quantitative value of ≤ 30 mg/dL in urinalysis or ≤ 1+ on dipstick, unless quantitative protein is < 1000 mg in a 24 hour urine sample
- Creatinine clearance > 40 mL/min per 24-hr urine collection or calculated according to the Cockcroft-Gault formula
Hepatic function, as follows:
- AST and ALT ≤ 2.5 x ULN per institutional laboratory range (or ≤ 5 x ULN if liver metastases are present)
- Total bilirubin ≤ 1.5x institutions' ULN Nutritional
- Albumin ≥ 2.8 g/dL
Exclusion Criteria:
- Prior use of anticancer therapy or experimental therapy for epithelial ovarian, primary peritoneal or fallopian tube cancers
- Previous abdominal and/or pelvic external beam radiotherapy
- Subjects believed to be a higher than average risk of bowel perforation. This includes current symptoms of partial or complete bowel obstruction, recent (within 6 months) history of fistula or bowel perforation, subjects requiring total parenteral nutrition and continuous hydration
- History of arterial or venous thromboembolism within 12 months prior to enrollment
- History of clinically significant bleeding within 6 months prior to enrollment
- History of central nervous system metastasis
- Known active or ongoing infection (except uncomplicated urinary tract infection) within 14 days prior to enrollment
- Currently or previously treated with AMG 386, or other molecules that inhibit the angiopoietins or Tie2 receptor
- Current or within 30 days prior to enrollment treatment with immune modulators such as systemic cyclosporine or tacrolimus
- Prior myeloablative high-dose chemotherapy with allogeneic or autologous stem cell (or bone marrow) transplant
- Clinically significant cardiac disease within 12 months prior to enrollment, including myocardial infarction, unstable angina, grade 2 or greater peripheral vascular disease, cerebrovascular accident, transient ischemic attack, congestive heart failure, or arrhythmias not controlled by outpatient medication or placement of percutaneous transluminal coronary angioplasty/stent
- Uncontrolled hypertension as defined as diastolic blood pressure > 90 mmHg OR systolic blood pressure > 140 mmHg. The use of anti-hypertensive medications to control hypertension is permitted
- Subjects with a history of prior malignancy, except:
Malignancy treated with curative intent and with no known active disease present for ≥ 3 years prior to enrollment and felt to be at low risk for recurrence by treating physician, Adequately treated non-melanomatous skin cancer or lentigo maligna without evidence of disease Adequately treated cervical carcinoma in situ without evidence of disease
- Major surgery within 28 days prior to enrollment or still recovering from prior surgery
- Minor surgical procedures, including placement of tunneled central venous access device, within 3 days prior to enrollment
- History of allergic reactions to bacterially-produced proteins
- Hypersensitivity to paclitaxel or drugs using the vehicle cremophor
- Pregnant (ie, positive beta-human chorionic gonadotropin test) or is breast feeding or planning to become pregnant within 6 months after the end of treatment
- Subject has known positive test(s) for human immunodeficiency virus (HIV) infection, hepatitis C virus, acute or chronic active hepatitis B infection
- Any condition which in the investigator's opinion makes the subject unsuitable for study participation
- Any uncontrolled concurrent illness or history of any medical condition that may interfere with the interpretation of the study results
- Non-healing wound, ulcer (including gastrointestinal) or fracture
- Subject has previously been enrolled onto this study
- Subject will not be available for follow-up assessment
- Subject has known sensitivity to any of the products to be administered during dosing
- Subject has any kind of disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures
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: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:AMG 386, paclitaxel and carboplatin
15 mg/Kg AMG 386 IV (intravenous) weekly plus paclitaxel and carboplatin IV Q3W for 18 weeks, followed by 15mg/Kg AMG 386 IV (intravenous) weekly alone for an additional 18 months.
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15 mg/Kg AMG 386 IV (intravenous) weekly plus paclitaxel and carboplatin IV Q3W for 18 weeks, followed by 15mg/Kg AMG 386 IV (intravenous) weekly alone for an additional 18 months.
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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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To evaluate whether AMG 386 in combination with paclitaxel and carboplatin is safe and well tolerated in the first-line treatment of high-risk stage I and stages II-IV epithelial ovarian, primary peritoneal and fallopian tube cancers.
時間枠:18 weeks of combination therapy
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18 weeks of combination therapy
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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To evaluate the pharmacokinetics (Cmax, AUC and Cmin) of AMG 386 in combination with carboplatin and paclitaxel
時間枠:Week 1 until Week 7
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Week 1 until Week 7
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To estimate the incidence of anti-AMG 386 antibody formation
時間枠:Week 1 until maximum of 1 year following first dose
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Week 1 until maximum of 1 year following first dose
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To evaluate the objective response rate (ORR) among subjects receiving AMG 386 in combination with carboplatin and paclitaxel
時間枠:From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
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From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
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To evaluate the duration of response (DOR) among subjects receiving AMG 386 in combination with carboplatin and paclitaxel
時間枠:From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
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From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
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To evaluate progression-free survival (PFS) among subjects receiving AMG 386 in combination with carboplatin and paclitaxel
時間枠:From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
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From date of first dose until the subject reaches End of Study. This will continue until 36 months after the last subject has been enrolled.
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To evaluate the number of participants with adverse events and clinical laboratory abnormalities
時間枠:96 weeks
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96 weeks
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To evaluate the effect of AMG 386 on the pharmacokinetics (Cmax, AUC and Cmin) of carboplatin and paclitaxel
時間枠:Week 1 until Week 7
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Week 1 until Week 7
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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。
スポンサー
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。
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
2010年11月1日
一次修了 (実際)
2012年10月1日
研究の完了 (実際)
2015年1月1日
試験登録日
最初に提出
2010年10月21日
QC基準を満たした最初の提出物
2010年12月2日
最初の投稿 (見積もり)
2010年12月3日
学習記録の更新
投稿された最後の更新 (見積もり)
2015年10月14日
QC基準を満たした最後の更新が送信されました
2015年10月13日
最終確認日
2015年10月1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。