- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01253681
Study of AMG 386 in Combination With Paclitaxel and Carboplatin in Subjects With Ovarian Cancer
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
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Phase 1
Kontakte und Standorte
Studienorte
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Victoria
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Footscray, Victoria, Australien, 3011
- Research Site
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Malvern, Victoria, Australien, 3144
- Research Site
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Parkville, Victoria, Australien, 3052
- Research Site
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Brussels, Belgien, 1000
- Research Site
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Bruxelles, Belgien, 1200
- Research Site
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Leuven, Belgien, 3000
- Research Site
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Madrid, Spanien, 28040
- Research Site
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Cataluña
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Barcelona, Cataluña, Spanien, 08035
- Research Site
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: 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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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
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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.
Zeitfenster: 18 weeks of combination therapy
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18 weeks of combination therapy
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
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To evaluate the pharmacokinetics (Cmax, AUC and Cmin) of AMG 386 in combination with carboplatin and paclitaxel
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: Week 1 until Week 7
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Week 1 until Week 7
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Mitarbeiter und Ermittler
Sponsor
Publikationen und hilfreiche Links
Nützliche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Neubildungen nach histologischem Typ
- Neubildungen
- Urogenitale Neoplasmen
- Neubildungen nach Standort
- Karzinom
- Neubildungen, Drüsen und Epithelien
- Genitale Neubildungen, weiblich
- Erkrankungen des endokrinen Systems
- Eierstockerkrankungen
- Adnexerkrankungen
- Gonadenstörungen
- Neoplasmen der endokrinen Drüse
- Eileitererkrankungen
- Eierstocktumoren
- Eileiterneoplasmen
- Karzinom, Eierstockepithel
- Physiologische Wirkungen von Arzneimitteln
- Molekulare Mechanismen der pharmakologischen Wirkung
- Antineoplastische Mittel
- Tubulin-Modulatoren
- Antimitotische Mittel
- Mitose-Modulatoren
- Antineoplastische Mittel, Phytogen
- Angiogenese-Inhibitoren
- Angiogenese-modulierende Mittel
- Wuchsstoffe
- Wachstumshemmer
- Carboplatin
- Paclitaxel
- Trebananib
Andere Studien-ID-Nummern
- 20090155
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