Ignite Creation Date:
2025-12-24 @ 3:04 PM
Ignite Modification Date:
2026-01-01 @ 3:34 AM
Study NCT ID:
NCT00807859
Status:
COMPLETED
Last Update Posted:
2022-11-08
First Post:
2008-12-11
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Safety Study of AMG 386 to Treat HER2-positive Locally Recurrent or Metastatic Breast Cancer
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D001943', 'term': 'Breast Neoplasms'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D009362', 'term': 'Neoplasm Metastasis'}], 'ancestors': [{'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D001941', 'term': 'Breast Diseases'}, {'id': 'D012871', 'term': 'Skin Diseases'}, {'id': 'D017437', 'term': 'Skin and Connective Tissue Diseases'}, {'id': 'D009385', 'term': 'Neoplastic Processes'}, {'id': 'D010335', 'term': 'Pathologic Processes'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C551398', 'term': 'trebananib'}, {'id': 'D017239', 'term': 'Paclitaxel'}, {'id': 'D000068878', 'term': 'Trastuzumab'}, {'id': 'D000069287', 'term': 'Capecitabine'}, {'id': 'D000077341', 'term': 'Lapatinib'}], 'ancestors': [{'id': 'D043823', 'term': 'Taxoids'}, {'id': 'D043822', 'term': 'Cyclodecanes'}, {'id': 'D003516', 'term': 'Cycloparaffins'}, {'id': 'D006840', 'term': 'Hydrocarbons, Alicyclic'}, {'id': 'D006844', 'term': 'Hydrocarbons, Cyclic'}, {'id': 'D006838', 'term': 'Hydrocarbons'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D004224', 'term': 'Diterpenes'}, {'id': 'D013729', 'term': 'Terpenes'}, {'id': 'D061067', 'term': 'Antibodies, Monoclonal, Humanized'}, {'id': 'D000911', 'term': 'Antibodies, Monoclonal'}, {'id': 'D000906', 'term': 'Antibodies'}, {'id': 'D007136', 'term': 'Immunoglobulins'}, {'id': 'D007162', 'term': 'Immunoproteins'}, {'id': 'D001798', 'term': 'Blood Proteins'}, {'id': 'D011506', 'term': 'Proteins'}, {'id': 'D000602', 'term': 'Amino Acids, Peptides, and Proteins'}, {'id': 'D012712', 'term': 'Serum Globulins'}, {'id': 'D005916', 'term': 'Globulins'}, {'id': 'D003841', 'term': 'Deoxycytidine'}, {'id': 'D003562', 'term': 'Cytidine'}, {'id': 'D011741', 'term': 'Pyrimidine Nucleosides'}, {'id': 'D011743', 'term': 'Pyrimidines'}, {'id': 'D006573', 'term': 'Heterocyclic Compounds, 1-Ring'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}, {'id': 'D005472', 'term': 'Fluorouracil'}, {'id': 'D014498', 'term': 'Uracil'}, {'id': 'D011744', 'term': 'Pyrimidinones'}, {'id': 'D003853', 'term': 'Deoxyribonucleosides'}, {'id': 'D009705', 'term': 'Nucleosides'}, {'id': 'D009706', 'term': 'Nucleic Acids, Nucleotides, and Nucleosides'}, {'id': 'D011799', 'term': 'Quinazolines'}, {'id': 'D006574', 'term': 'Heterocyclic Compounds, 2-Ring'}, {'id': 'D000072471', 'term': 'Heterocyclic Compounds, Fused-Ring'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 65}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2009-03-09', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2022-11', 'completionDateStruct': {'date': '2015-10-19', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2022-11-04', 'studyFirstSubmitDate': '2008-12-11', 'studyFirstSubmitQcDate': '2008-12-11', 'lastUpdatePostDateStruct': {'date': '2022-11-08', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2008-12-12', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2014-02-27', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Primary objective is to identify the incidence of adverse events and clinical laboratory abnormalities defined as a dose limiting toxicity in subjects treated with AMG 386 plus paclitaxel and trastuzumab or with AMG 386 plus capecitabine and lapatinib', 'timeFrame': '24 months'}], 'secondaryOutcomes': [{'measure': 'To evaluate the incidence of adverse events and clinical laboratory abnormalities not defined as DLTs', 'timeFrame': '24 months'}, {'measure': 'To evaluate the pharmacokinetics (PK) of AMG 386, trastuzumab, and paclitaxel (cohort A) or AMG 386, lapatinib, and capecitabine (and its active metabolite, 5-FU; cohort B) when administered in combination', 'timeFrame': '24 months'}, {'measure': 'To estimate the incidence of anti AMG 386 antibody formation', 'timeFrame': '24 months'}, {'measure': 'To evaluate the treatment effect as measured by the following: objective response rate (ORR), duration of response (DOR), change in tumor burden and progression-free survival (PFS)', 'timeFrame': '23 months'}]}, 'conditionsModule': {'keywords': ['AMG 386', 'Paclitaxel', 'Trastuzumab', 'Capecitabine', 'Lapatinib', 'HER2-positive', 'metastatic breast cancer', 'locally recurrent breast cancer', 'Taxol', 'Herceptin', 'Xeloda', 'Tykerb', 'anti-angiogenic therapy'], 'conditions': ['Breast Cancer', 'Breast Neoplasms', 'Breast Tumors', 'Cancer', 'Locally Recurrent and Metastatic Breast Cancer', 'Metastases', 'Metastatic Cancer', 'Oncology', 'Solid Tumors', 'Tumors']}, 'referencesModule': {'references': [{'pmid': '30420181', 'type': 'BACKGROUND', 'citation': 'Kaufman PA, Wildiers H, Freyer G, Kemeny M, Goncalves A, Jerusalem G, Stopeck A, Vrindavanam N, Dalenc F, Nanayakkara N, Wu B, Pickett CA. Phase 1b Study of Trebananib Plus Paclitaxel and Trastuzumab in Patients With HER2-Positive Locally Recurrent or Metastatic Breast Cancer. Clin Breast Cancer. 2019 Feb;19(1):47-57. doi: 10.1016/j.clbc.2018.09.012. Epub 2018 Oct 9.'}], 'seeAlsoLinks': [{'url': 'http://www.amgentrials.com', 'label': 'AmgenTrials clinical trials website'}]}, 'descriptionModule': {'briefSummary': 'The purpose of this study is to determine if AMG 386 in combination with either paclitaxel and trastuzumab or capecitabine and lapatinib is safe and well tolerated in subjects with HER2-positive locally recurrent or metastatic breast cancer.\n\nThis is an open-label phase 1b trial and has 2 study parts. Study part 1 is a dose escalation study to determine a tolerable dose of AMG 386 in combination with paclitaxel and trastuzumab (cohort A) or with capecitabine and lapatinib (cohort B). Study part 2 is cohort expansion of the tolerable doses determined in part 1.'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* histologically or cytologically confirmed adenocarcinoma of the breast with locally recurrent or metastatic disease not amenable to any local treatment with curative intent.\n* HER2-positive by FISH, CISH, or IHC 3+\n* ECOG performance status 0 or 1\n* Left ventricular ejection fraction greater than or equal to institutional lower limit of normal\n* Adequate laboratory studies (hematological, chemistries and urinalysis)\n* Life expectancy greater than or equal to 3 months\n* Cohort A only:\n* Trastuzumab naïve or trastuzumab in the neo-adjuvant setting\n* No clinically significant drop in cardiac function prior exposure to trastuzumab\n* No prior chemotherapy for metastatic or locally recurrent breast cancer\n* No prior lapatinib therapy\n* At least 3 weeks from enrollment since prior chemotherapeutic agents, including taxanes, in the neoadjuvant or adjuvant setting\n* At least 3 months from enrollment since prior trastuzumab in the neoadjuvant or adjuvant setting\n* Cohort B only:\n* Must have failed trastuzumab in the first-line metastatic setting. Trastuzumab must be discontinued for at least 3 weeks prior to enrollment\n* Must have received prior chemotherapy as adjuvant therapy or for metastatic disease\n* Prior chemotherapy treatment must be discontinued for at least 3 weeks prior to enrollment\n* No prior capecitabine\n* No prior lapatinib\n\nExclusion Criteria:\n\n* Inflammatory breast cancer\n* Central nervous system metastasis\n* Clinically significant cardiovascular disease\n* Radiation therapy ≤ 14 days prior to enrollment.\n* Concurrent anticoagulation therapy, excluding aspirin, anti-platelet agents, low molecular weight heparin or low dose warfarin per protocol.\n* Uncontrolled hypertension defined as diastolic blood pressure \\> 90 mmHg OR systolic blood pressure \\> 140 mmHg.\n* Subjects with a history of prior malignancy, except:\n* For Cohort B only:\n* Current or prior history of long QT syndrome\n* Baseline ECG report of QTc interval of \\> 480 milliseconds\n* Severe chronic liver disease (Child Pugh C)'}, 'identificationModule': {'nctId': 'NCT00807859', 'briefTitle': 'Safety Study of AMG 386 to Treat HER2-positive Locally Recurrent or Metastatic Breast Cancer', 'organization': {'class': 'INDUSTRY', 'fullName': 'Amgen'}, 'officialTitle': 'An Open-Label Study of AMG 386 in Combination With Either Paclitaxel and Trastuzumab or Capecitabine and Lapatinib in Subjects With HER2-positive Locally Recurrent or Metastatic Breast Cancer', 'orgStudyIdInfo': {'id': '20062042'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Cohort A1', 'interventionNames': ['Drug: AMG 386 10 mgkg, Paclitaxel and Trastuzumab']}, {'type': 'EXPERIMENTAL', 'label': 'Cohort A3', 'interventionNames': ['Drug: AMG 386 30 mg/kg, Paclitaxel and Trastuzumab']}, {'type': 'EXPERIMENTAL', 'label': 'Cohort B1', 'interventionNames': ['Drug: AMG 386 10 mg/kg, Capecitabine and Lapatinib']}, {'type': 'EXPERIMENTAL', 'label': 'Cohort B3', 'interventionNames': ['Drug: AMG 386 30 mg/kg, Capecitabine and Lapatinib']}], 'interventions': [{'name': 'AMG 386 30 mg/kg, Paclitaxel and Trastuzumab', 'type': 'DRUG', 'description': 'AMG 386 30 mg/kg IV QW, paclitaxel 80 mg/m2 IV QW, trastuzumab: initial dose 8 mg/kg IV week 1, then 6 mg/kg IV Q3W', 'armGroupLabels': ['Cohort A3']}, {'name': 'AMG 386 30 mg/kg, Capecitabine and Lapatinib', 'type': 'DRUG', 'description': 'AMG 386 30 mg/kg IV QW, capecitabine 2000 mg/m2 divided into 2 doses given PO Q12 hrs, days 1-14 every 21 days, lapatinib 1250 mg PO QD', 'armGroupLabels': ['Cohort B3']}, {'name': 'AMG 386 10 mgkg, Paclitaxel and Trastuzumab', 'type': 'DRUG', 'description': 'AMG 386 10 mg/kg IV QW, paclitaxel 80 mg/m2 IV QW, trastuzumab: initial dose 8 mg/kg IV week 1, then 6 mg/kg IV Q3W', 'armGroupLabels': ['Cohort A1']}, {'name': 'AMG 386 10 mg/kg, Capecitabine and Lapatinib', 'type': 'DRUG', 'description': 'AMG 386 10 mg/kg IV QW, capecitabine 2000 mg/m2 divided into 2 doses given PO Q12 hrs, days 1-14 every 21 days, lapatinib 1250 mg PO QD', 'armGroupLabels': ['Cohort B1']}]}, 'contactsLocationsModule': {'locations': [{'zip': '85724', 'city': 'Tucson', 'state': 'Arizona', 'country': 'United States', 'facility': 'Research Site', 'geoPoint': {'lat': 32.22174, 'lon': -110.92648}}, {'zip': '33428', 'city': 'Boca Raton', 'state': 'Florida', 'country': 'United States', 'facility': 'Research Site', 'geoPoint': {'lat': 26.35869, 'lon': -80.0831}}, {'zip': '52242', 'city': 'Iowa City', 'state': 'Iowa', 'country': 'United States', 'facility': 'Research Site', 'geoPoint': {'lat': 41.66113, 'lon': -91.53017}}, {'zip': '02111', 'city': 'Boston', 'state': 'Massachusetts', 'country': 'United States', 'facility': 'Research Site', 'geoPoint': {'lat': 42.35843, 'lon': -71.05977}}, {'zip': '55407', 'city': 'Minneapolis', 'state': 'Minnesota', 'country': 'United States', 'facility': 'Research Site', 'geoPoint': {'lat': 44.97997, 'lon': -93.26384}}, {'zip': '03756-0001', 'city': 'Lebanon', 'state': 'New Hampshire', 'country': 'United 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