Viewing Study NCT05253651


Ignite Creation Date: 2025-12-24 @ 11:39 PM
Ignite Modification Date: 2025-12-25 @ 9:29 PM
Study NCT ID: NCT05253651
Status: RECRUITING
Last Update Posted: 2025-12-17
First Post: 2022-02-14
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Study of Tucatinib With Trastuzumab and mFOLFOX6 Versus Standard of Care Treatment in First-line HER2+ Metastatic Colorectal Cancer
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'removedCountries': ['Hungary']}, 'conditionBrowseModule': {'meshes': [{'id': 'D015179', 'term': 'Colorectal Neoplasms'}], 'ancestors': [{'id': 'D007414', 'term': 'Intestinal Neoplasms'}, {'id': 'D005770', 'term': 'Gastrointestinal Neoplasms'}, {'id': 'D004067', 'term': 'Digestive System Neoplasms'}, {'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D004066', 'term': 'Digestive System Diseases'}, {'id': 'D005767', 'term': 'Gastrointestinal Diseases'}, {'id': 'D003108', 'term': 'Colonic Diseases'}, {'id': 'D007410', 'term': 'Intestinal Diseases'}, {'id': 'D012002', 'term': 'Rectal Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C000705452', 'term': 'tucatinib'}, {'id': 'D000068878', 'term': 'Trastuzumab'}, {'id': 'D000068258', 'term': 'Bevacizumab'}, {'id': 'D000068818', 'term': 'Cetuximab'}, {'id': 'D000077150', 'term': 'Oxaliplatin'}, {'id': 'D002955', 'term': 'Leucovorin'}, {'id': 'D058766', 'term': 'Levoleucovorin'}, {'id': 'D005472', 'term': 'Fluorouracil'}], 'ancestors': [{'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': 'D056831', 'term': 'Coordination Complexes'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D005575', 'term': 'Formyltetrahydrofolates'}, {'id': 'D013763', 'term': 'Tetrahydrofolates'}, {'id': 'D005492', 'term': 'Folic Acid'}, {'id': 'D011622', 'term': 'Pterins'}, {'id': 'D011621', 'term': 'Pteridines'}, {'id': 'D006574', 'term': 'Heterocyclic Compounds, 2-Ring'}, {'id': 'D000072471', 'term': 'Heterocyclic Compounds, Fused-Ring'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}, {'id': 'D003067', 'term': 'Coenzymes'}, {'id': 'D045762', 'term': 'Enzymes and Coenzymes'}, {'id': 'D014498', 'term': 'Uracil'}, {'id': 'D011744', 'term': 'Pyrimidinones'}, {'id': 'D011743', 'term': 'Pyrimidines'}, {'id': 'D006573', 'term': 'Heterocyclic Compounds, 1-Ring'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 400}}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2022-10-24', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-12', 'completionDateStruct': {'date': '2029-07-27', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-12-10', 'studyFirstSubmitDate': '2022-02-14', 'studyFirstSubmitQcDate': '2022-02-14', 'lastUpdatePostDateStruct': {'date': '2025-12-17', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2022-02-24', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2026-04-03', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) by Blinded Independent Central Review (BICR)', 'timeFrame': 'Up to approximately 3 years', 'description': 'The time from the date of randomization to the BICR assessment of disease progression according to RECIST v1.1 or death from any cause'}], 'secondaryOutcomes': [{'measure': 'Overall survival (OS)', 'timeFrame': 'Up to approximately 6 years', 'description': 'The time from randomization to death from any cause'}, {'measure': 'Confirmed objective response rate (cORR) per RECIST v1.1 by BICR', 'timeFrame': 'Up to approximately 3 years', 'description': 'The proportion of participants with confirmed complete response (CR) or partial response (PR) according to RECIST v1.1, as assessed by BICR'}, {'measure': 'PFS per RECIST v1.1 by investigator assessment', 'timeFrame': 'Up to approximately 3 years', 'description': 'The time from the date of randomization to the investigator assessment of disease progression according to RECIST v1.1 or death from any cause'}, {'measure': 'cORR per RECIST v1.1 by investigator assessment', 'timeFrame': 'Up to approximately 3 years', 'description': 'The proportion of participants with confirmed CR or PR according to RECIST v1.1, as assessed by investigators'}, {'measure': 'Duration of response (DOR) per RECIST v1.1 by BICR', 'timeFrame': 'Up to approximately 3 years', 'description': 'The time from first documentation of objective response (CR or PR that is subsequently confirmed) to the first documentation of disease progression per RECIST v1.1 or death from any cause'}, {'measure': 'DOR per RECIST v1.1 by investigator assessment', 'timeFrame': 'Up to approximately 3 years', 'description': 'The time from first documentation of objective response (CR or PR that is subsequently confirmed) to the first documentation of disease progression per RECIST v1.1 or death from any cause'}, {'measure': 'Time to second progression or death (PFS2)', 'timeFrame': 'Up to approximately 3 years', 'description': 'The time from randomization to disease progression on the next-line of therapy, or death from any cause'}, {'measure': 'Incidence of adverse events (AEs)', 'timeFrame': 'Through 30 days after the last study treatment; approximately 1 year', 'description': 'Any untoward medical occurrence in a clinical investigational participant administered a medicinal product and which does not necessarily have a causal relationship with this treatment.'}, {'measure': 'Incidence of dose alterations', 'timeFrame': 'Through 30 days after the last study treatment; approximately 1 year'}, {'measure': 'Trough concentration (Ctrough)', 'timeFrame': 'Approximately 4 months', 'description': 'PK parameter'}, {'measure': 'Change from baseline in European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30 (EORTC QLQC30) score', 'timeFrame': 'Through 30-37 days after the last study treatment; approximately 1 year', 'description': 'Change from baseline in European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) scores. Scale scores range from 0-100. For functioning and global health status/quality of life (QoL) scales, higher scores indicate better functioning or global health status/quality of life (QoL). For symptom scales, higher scores indicate greater symptom burden.'}, {'measure': 'Time to meaningful change in EORTC QLQ30 score', 'timeFrame': 'Through 30-37 days after the last study treatment; approximately 1 year', 'description': 'The time from baseline to the first onset of a ≥10-point changes in European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) scores. Scale scores range from 0-100.\n\nFor functioning and global health status/QoL scales, higher scores indicate better functioning or global health status/QoL. For symptom scales, higher scores indicate greater symptom burden.'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Colorectal Cancer', 'CRC', 'Seattle Genetics'], 'conditions': ['Colorectal Neoplasms']}, 'referencesModule': {'references': [{'pmid': '39723627', 'type': 'DERIVED', 'citation': 'Strickler JH, Bekaii-Saab T, Cercek A, Heinemann V, Nakamura Y, Raghav K, Siena S, Tabernero J, Van Cutsem E, Yoshino T, Ramos J, Guan X, Andre T. MOUNTAINEER-03 phase III study design: first-line mFOLFOX6 + tucatinib + trastuzumab for HER2+ metastatic colorectal cancer. Future Oncol. 2025 Feb;21(3):303-311. doi: 10.1080/14796694.2024.2441101. Epub 2024 Dec 26.'}], 'seeAlsoLinks': [{'url': 'https://pmiform.com/clinical-trial-info-request?StudyID=SGNTUC-029', 'label': 'To obtain contact information for a study center near you, click here.'}]}, 'descriptionModule': {'briefSummary': 'This study is being done to find out if tucatinib with other cancer drugs works better than standard of care to treat participants with HER2 positive colorectal cancer. This study will also determine what side effects happen when participants take this combination of drugs. A side effect is anything a drug does to the body besides treating your disease.\n\nParticipants in this study have colorectal cancer that has spread through the body (metastatic) and/or cannot be removed with surgery (unresectable).\n\nParticipants will be assigned randomly to the tucatinib group or standard of care group. The tucatinib group will get tucatinib, trastuzumab, and mFOLFOX6. The standard of care group will get either:\n\n* mFOLFOX6 alone,\n* mFOLFOX6 with bevacizumab, or\n* mFOLFOX6 with cetuximab mFOLFOX6 is a combination of multiple drugs. All of the drugs given in this study are used to treat this type of cancer.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Histologically and/or cytologically confirmed adenocarcinoma of the colon or rectum which is locally advanced unresectable or metastatic\n* Able to provide the most recently available formalin-fixed paraffin-embedded (FFPE) tumor tissue blocks (or freshly sectioned slides) obtained prior to treatment initiation to a central laboratory\n\n * If archival tissue is not available, a newly-obtained baseline biopsy of an accessible tumor lesion is required within 35 days prior to start of study treatment\n* HER2+ disease as determined by a tissue based assay performed at a central laboratory.\n* Participant has rat sarcoma viral oncogene homolog wild-type (RAS WT) disease as determined by local or central testing. For central RAS analysis, tissue sample must be analyzed within 1 year of biopsy date.\n* Radiographically measurable disease per RECIST v1.1 with:\n\n * At least one site of disease that is measurable and that has not been previously irradiated, or\n * If the participant has had previous radiation to the target lesion(s), there must be evidence of progression since the radiation\n* Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1\n* CNS Inclusion - based on contrast brain magnetic resonance imaging, participants may have any of the following:\n\n * No evidence of brain metastases\n * Previously treated brain metastases which are asymptomatic\n\nExclusion Criteria:\n\n* Prior systemic anticancer therapy for colorectal cancer (CRC) in the locally advanced unresectable or metastatic setting; note that participants may have received a maximum of 2 doses of mFOLFOX6 in the locally advanced/unresectable or metastatic setting prior to randomization.\n\n * Note: May have received chemotherapy for CRC in the adjuvant setting if it was completed \\>6 months prior to enrollment\n* Radiation therapy within 14 days prior to enrollment (or within 7 days in the setting of stereotactic radiosurgery)\n* Previous treatment with anti-HER2 therapy\n* Ongoing Grade 3 or higher neuropathy\n* Active or untreated gastrointestinal (GI) perforation at the time of screening.'}, 'identificationModule': {'nctId': 'NCT05253651', 'acronym': 'MOUNTAINEER-03', 'briefTitle': 'A Study of Tucatinib With Trastuzumab and mFOLFOX6 Versus Standard of Care Treatment in First-line HER2+ Metastatic Colorectal Cancer', 'organization': {'class': 'INDUSTRY', 'fullName': 'Seagen Inc.'}, 'officialTitle': 'An Open-label Randomized Phase 3 Study of Tucatinib in Combination With Trastuzumab and mFOLFOX6 Versus mFOLFOX6 Given With or Without Either Cetuximab or Bevacizumab as First-line Treatment for Subjects With HER2+ Metastatic Colorectal Cancer', 'orgStudyIdInfo': {'id': 'SGNTUC-029'}, 'secondaryIdInfos': [{'id': 'C4251008', 'type': 'OTHER', 'domain': 'Alias Study Number'}, {'id': '2024-514180-25-00', 'type': 'REGISTRY', 'domain': 'CTIS (EU)'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Tucatinib Arm', 'description': 'Tucatinib + trastuzumab + mFOLFOX6', 'interventionNames': ['Drug: tucatinib', 'Drug: trastuzumab', 'Drug: oxaliplatin', 'Drug: leucovorin', 'Drug: levoleucovorin', 'Drug: fluorouracil']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Standard of Care Arm', 'description': 'Either (1) mFOLFOX6, (2) mFOLFOX6 and bevacizumab, or (3) mFOLFOX6 and cetuximab', 'interventionNames': ['Drug: bevacizumab', 'Drug: cetuximab', 'Drug: oxaliplatin', 'Drug: leucovorin', 'Drug: levoleucovorin', 'Drug: fluorouracil']}], 'interventions': [{'name': 'tucatinib', 'type': 'DRUG', 'otherNames': ['TUKYSA, ONT-380, ARRY-380, PF-07265792'], 'description': '300mg given by mouth (orally) twice daily', 'armGroupLabels': ['Tucatinib Arm']}, {'name': 'trastuzumab', 'type': 'DRUG', 'otherNames': ['Herceptin'], 'description': '8mg/kg loading dose will be given into the vein (IV; intravenously) on Cycle 1 day 1, followed by 6mg/kg given by IV every 3 weeks thereafter.', 'armGroupLabels': ['Tucatinib Arm']}, {'name': 'bevacizumab', 'type': 'DRUG', 'otherNames': ['Avastin'], 'description': '5mg/kg given by IV every 2 weeks', 'armGroupLabels': ['Standard of Care Arm']}, {'name': 'cetuximab', 'type': 'DRUG', 'otherNames': ['Erbitux'], 'description': '400mg/m2 loading dose will be given by IV on Cycle 1 day 1, followed by 250mg/m2 given by IV weekly', 'armGroupLabels': ['Standard of Care Arm']}, {'name': 'oxaliplatin', 'type': 'DRUG', 'description': '85mg/m2 given by IV every 2 weeks. Component of mFOLFOX6.', 'armGroupLabels': ['Standard of Care Arm', 'Tucatinib Arm']}, {'name': 'leucovorin', 'type': 'DRUG', 'description': '400mg/ m2 given by IV every 2 weeks. Component of mFOLFOX6.', 'armGroupLabels': ['Standard of Care Arm', 'Tucatinib Arm']}, {'name': 'levoleucovorin', 'type': 'DRUG', 'description': '200mg/ m2 given by IV every 2 weeks. May be given in place of leucovorin. Component of mFOLFOX6.', 'armGroupLabels': ['Standard of Care Arm', 'Tucatinib Arm']}, {'name': 'fluorouracil', 'type': 'DRUG', 'description': '400mg/m2 given by IV bolus then 2400mg/m2 given by continuous IV infusion (over 46-48 hours) every 2 weeks. Component of mFOLFOX6.', 'armGroupLabels': ['Standard of Care Arm', 'Tucatinib Arm']}]}, 'contactsLocationsModule': {'locations': [{'zip': '85304', 'city': 'Glendale', 'state': 'Arizona', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Palo Verde Hematology Oncology', 'geoPoint': {'lat': 33.53865, 'lon': -112.18599}}, {'zip': '85054', 'city': 'Phoenix', 'state': 'Arizona', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Mayo Clinic Building - Phoenix', 'geoPoint': {'lat': 33.44838, 'lon': -112.07404}}, {'zip': '85054', 'city': 'Phoenix', 'state': 'Arizona', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Mayo Clinic Hospital', 'geoPoint': {'lat': 33.44838, 'lon': -112.07404}}, {'zip': '85259', 'city': 'Scottsdale', 'state': 'Arizona', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Mayo Clinic', 'geoPoint': {'lat': 33.50921, 'lon': -111.89903}}, {'zip': '92801', 'city': 'Anaheim', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Los Angeles Cancer Network - Anaheim', 'geoPoint': {'lat': 33.83529, 'lon': -117.9145}}, {'zip': '92806', 'city': 'Anaheim', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Anaheim Kraemer Medical Offices', 'geoPoint': {'lat': 33.83529, 'lon': -117.9145}}, {'zip': '91706', 'city': 'Baldwin Park', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Baldwin Park Medical Center', 'geoPoint': {'lat': 34.08529, 'lon': -117.9609}}, {'zip': '90706', 'city': 'Bellflower', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Bellflower Medical Offices', 'geoPoint': {'lat': 33.88168, 'lon': -118.11701}}, {'zip': '92335', 'city': 'Fontana', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Fontana Medical Center', 'geoPoint': {'lat': 34.09223, 'lon': -117.43505}}, {'zip': '92708', 'city': 'Fountain Valley', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Los Angeles Cancer Network - Fountain Vally', 'geoPoint': {'lat': 33.70918, 'lon': -117.95367}}, {'zip': '91204', 'city': 'Glendale', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Los Angeles Hematology Oncology Medical Group', 'geoPoint': {'lat': 34.14251, 'lon': -118.25508}}, {'zip': '91206', 'city': 'Glendale', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Los Angeles Hematology Oncology Medical Group', 'geoPoint': {'lat': 34.14251, 'lon': -118.25508}}, {'zip': '90710', 'city': 'Harbor City', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente South Bay Medical center', 'geoPoint': {'lat': 33.79002, 'lon': -118.29785}}, {'zip': '92618', 'city': 'Irvine', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Alton/Sand Canyon Medical Offices', 'geoPoint': {'lat': 33.66946, 'lon': -117.82311}}, {'zip': '90017', 'city': 'Los Angeles', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Los Angeles Hematology Oncology Medical Group', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '90020', 'city': 'Los Angeles', 'state': 'California', 'status': 'TERMINATED', 'country': 'United States', 'facility': 'USC Norris Koreatown - Medical Oncology', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '90027', 'city': 'Los Angeles', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Los Angeles Medical Offices', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '90033', 'city': 'Los Angeles', 'state': 'California', 'status': 'TERMINATED', 'country': 'United States', 'facility': 'Keck Hospital of USC', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '90033', 'city': 'Los Angeles', 'state': 'California', 'status': 'TERMINATED', 'country': 'United States', 'facility': 'Los Angeles General Medical Center', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '90033', 'city': 'Los Angeles', 'state': 'California', 'status': 'TERMINATED', 'country': 'United States', 'facility': 'University of Southern California', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '90033', 'city': 'Los Angeles', 'state': 'California', 'status': 'TERMINATED', 'country': 'United States', 'facility': 'USC/Norris Comprehensive Cancer Center', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '90034', 'city': 'Los Angeles', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente West Los Angeles Medical Center', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '92663', 'city': 'Newport Beach', 'state': 'California', 'status': 'TERMINATED', 'country': 'United States', 'facility': 'USC Norris Oncology/Hematology - Newport Beach', 'geoPoint': {'lat': 33.61891, 'lon': -117.92895}}, {'zip': '91761', 'city': 'Ontario', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Ontario Medical Center', 'geoPoint': {'lat': 34.06334, 'lon': -117.65089}}, {'zip': '91402', 'city': 'Panorama City', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Panorama City Medical Center', 'geoPoint': {'lat': 34.22473, 'lon': -118.44981}}, {'zip': '91105', 'city': 'Pasadena', 'state': 'California', 'status': 'TERMINATED', 'country': 'United States', 'facility': 'Keck Medical Center of USC Pasadena', 'geoPoint': {'lat': 34.14778, 'lon': -118.14452}}, {'zip': '91105', 'city': 'Pasadena', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Los Angeles Hematology Oncology Medical Group', 'geoPoint': {'lat': 34.14778, 'lon': -118.14452}}, {'zip': '92505', 'city': 'Riverside', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Riverside Medical Center', 'geoPoint': {'lat': 33.95335, 'lon': -117.39616}}, {'zip': '92108', 'city': 'San Diego', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente San Diego Mission Road (Regulatory and Lab Supplies)', 'geoPoint': {'lat': 32.71571, 'lon': -117.16472}}, {'zip': '92120', 'city': 'San Diego', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Zion Medical Center', 'geoPoint': {'lat': 32.71571, 'lon': -117.16472}}, {'zip': '92078', 'city': 'San Marcos', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente San Marcos Medical Offices', 'geoPoint': {'lat': 33.14337, 'lon': -117.16614}}, {'zip': '91405', 'city': 'Van Nuys', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Los Angeles Hematology Oncology Medical Group', 'geoPoint': {'lat': 34.18667, 'lon': -118.44897}}, {'zip': '91367', 'city': 'Woodland Hills', 'state': 'California', 'status': 'ACTIVE_NOT_RECRUITING', 'country': 'United States', 'facility': 'Kaiser Permanente Woodland Hills Medical Center', 'geoPoint': {'lat': 34.16834, 'lon': -118.60592}}, {'zip': '80012', 'city': 'Aurora', 'state': 'Colorado', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Rocky Mountain Cancer Centers, LLP', 'geoPoint': {'lat': 39.72943, 'lon': -104.83192}}, {'zip': '80303', 'city': 'Boulder', 'state': 'Colorado', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Rocky Mountain Cancer Centers, LLP', 'geoPoint': {'lat': 40.01499, 'lon': -105.27055}}, {'zip': '80907', 'city': 'Colorado Springs', 'state': 'Colorado', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Rocky Mountain Cancer Centers, LLP', 'geoPoint': {'lat': 38.83388, 'lon': -104.82136}}, {'zip': '80218', 'city': 'Denver', 'state': 'Colorado', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Rocky Mountain Cancer Centers, LLP', 'geoPoint': {'lat': 39.73915, 'lon': -104.9847}}, {'zip': '80220', 'city': 'Denver', 'state': 'Colorado', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Rocky Mountain Cancer Centers, LLP', 'geoPoint': {'lat': 39.73915, 'lon': -104.9847}}, {'zip': '80228', 'city': 'Lakewood', 'state': 'Colorado', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Rocky Mountain Cancer Centers, LLP', 'geoPoint': {'lat': 39.70471, 'lon': -105.08137}}, {'zip': '80120', 'city': 'Littleton', 'state': 'Colorado', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Rocky Mountain 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