Ignite Creation Date:
2025-12-26 @ 2:39 PM
Ignite Modification Date:
2026-07-13 @ 12:47 AM
Study NCT ID:
NCT02489006
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-01-17
First Post:
2015-04-17
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
A Study of Olaparib Prior to Surgery and Chemotherapy in Ovarian, Primary Peritoneal, and Fallopian Tube Cancer
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D010051', 'term': 'Ovarian Neoplasms'}, {'id': 'D005185', 'term': 'Fallopian Tube Neoplasms'}], 'ancestors': [{'id': 'D004701', 'term': 'Endocrine Gland Neoplasms'}, {'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D010049', 'term': 'Ovarian Diseases'}, {'id': 'D000291', 'term': 'Adnexal Diseases'}, {'id': 'D005831', 'term': 'Genital Diseases, Female'}, {'id': 'D052776', 'term': 'Female Urogenital Diseases'}, {'id': 'D005261', 'term': 'Female Urogenital Diseases and Pregnancy Complications'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D005833', 'term': 'Genital Neoplasms, Female'}, {'id': 'D014565', 'term': 'Urogenital Neoplasms'}, {'id': 'D000091662', 'term': 'Genital Diseases'}, {'id': 'D004700', 'term': 'Endocrine System Diseases'}, {'id': 'D006058', 'term': 'Gonadal Disorders'}, {'id': 'D005184', 'term': 'Fallopian Tube Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C531550', 'term': 'olaparib'}, {'id': 'D017671', 'term': 'Platinum Compounds'}], 'ancestors': [{'id': 'D007287', 'term': 'Inorganic Chemicals'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 71}}, 'statusModule': {'overallStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2016-07-19', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2024-01', 'completionDateStruct': {'date': '2025-12-31', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2024-01-14', 'studyFirstSubmitDate': '2015-04-17', 'studyFirstSubmitQcDate': '2015-06-30', 'lastUpdatePostDateStruct': {'date': '2024-01-17', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2015-07-02', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2025-12-31', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Difference in levels of PAR or PARP-1 before and after study treatment', 'timeFrame': '4-8 weeks'}, {'measure': 'Mutations in BRCA1/2, RAD51B, RAD51C, RAD51D, PPM1D, FANCM, BRIP1, PALB2 and BARD1 in germline tissue compared to tumor tissue', 'timeFrame': '2.5 years'}], 'secondaryOutcomes': [{'measure': 'Frequency of adverse events, by description and grade', 'timeFrame': '2.5 years'}, {'measure': 'Response rate to olaparib in the neoadjuvant period', 'timeFrame': '6 weeks'}, {'measure': 'Duration of progression free survival with olaparib in comparison to platinum based chemotherapy', 'timeFrame': '2.5 years'}, {'measure': 'Levels of ctDNA compared to levels of CA125', 'timeFrame': '2.5 years'}, {'measure': 'Gene expression changes in tumour tissue before and after treatment with Olaparib', 'timeFrame': '2.5 years'}, {'measure': 'Secondary mutation rate in surgical tumour specimens following PARP therapy and at progression', 'timeFrame': '2.5 years', 'description': '2.5 years'}, {'measure': 'Changes in blood based biomarkers using ctDNA before, during and after treatment with Olaparib', 'timeFrame': '2.5 years'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'conditions': ['Ovarian Cancer', 'Fallopian Tube Cancer', 'Neoadjuvant Treatment', 'Debulking Surgical Procedures']}, 'descriptionModule': {'briefSummary': 'This is a study that will look at the effects and how useful investigational drug olaparib is as a neoadjuvant treatment (treatment given as to shrink a tumor before the main treatment) prior to surgery in patients with recurrent ovarian, primary peritoneal or fallopian tube cancer.', 'detailedDescription': 'Olaparib belongs to a class of anti-cancer agents known as poly ADP-ribose polymerase (PARP) inhibitors. Olaparib is a new type of drug for ovarian cancer. Laboratory tests show that it may help slow the growth of ovarian cancer.\n\nOlaparib works by blocking the PARP protein. PARP is an important protein which tries to fix damaged deoxyribonucleic acid (DNA, molecules that contain important instructions for the development of cells). Many cancers are thought to develop from damaged DNA. Research has shown that PARP inhibitors stop the PARP protein from working, and that sometimes that can cause cancer cells to stop growing or die.'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Histologically proven recurrent high grade serous ovarian/primary peritoneal or fallopian tube cancer.\n* Patients must have disease amenable to pre-operative biopsy.\n* Patients must have disease deemed suitable for surgical debulking.\n* Patients must have a progression free interval of at least 6 months prior to registration.\n* Patients must have had at least one line of platinum based therapy.\n* Patients must have shown platinum sensitivity to their last line of platinum therapy\n* Age \\>=18 years\n* ECOG performance status 0-1 within 7 days of registration\n* Life expectancy of greater than 3 months\n* Patients must have normal organ and marrow function\n* Women of child-bearing potential must agree to use adequate contraception prior to study entry and for the duration of study participation.\n* Ability to understand and the willingness to sign a written informed consent document.\n* Subject's willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.\n\nExclusion Criteria:\n\n* History of allergic reactions attributed to compounds of similar chemical or biologic composition to olaparib.\n* History of allergic reactions attributed to platinum precluding further use.\n* Radiation therapy within 4 weeks of registration\n* Use of any other systemic, targeted, immunotherapy, chemotherapy, or investigational agents within 4 weeks of registration\n* Previously received a PARP inhibitor\n* Other malignancy within the last 2 years with exceptions\n* Patients considered a poor medical risk due to a serious, uncontrolled medical disorder, non-malignant systemic disease or active, uncontrolled infection.\n* Patients unable to swallow orally administered medication and patients with gastrointestinal disorders likely to interfere with absorption of the study medication.\n* Concomitant use of known potent CYP3A4 inhibitors\n* Concomitant use of known potent CYP3A4 inducers\n* Other anti-cancer therapy including immunotherapy, hormonal therapy, biological therapy, other novel agents or investigational agents\n* Persistent toxicities (CTCAE v 4.03 grade \\>2) caused by previous cancer therapy, excluding alopecia\n* Patients with myelodysplastic syndrome/acute myeloid leukemia\n* Patients with brain metastases\n* Immunocompromised patients, e.g., patients who are known to be serologically positive for human immunodeficiency virus (HIV)\n* Patients with known active hepatitis (i.e., hepatitis B or C) due to risk of transmitting the infection through blood or other body fluids\n* Pregnant or breastfeeding women\n* Receipt of live attenuated vaccine within 30 days prior to enrollment\n* Patients with \\> Grade 2 hearing impairment as per CTCAE v 4.03\n* Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results, and in the judgment of the investigator would make the subject inappropriate for entry into this study."}, 'identificationModule': {'nctId': 'NCT02489006', 'acronym': 'NEO', 'briefTitle': 'A Study of Olaparib Prior to Surgery and Chemotherapy in Ovarian, Primary Peritoneal, and Fallopian Tube Cancer', 'organization': {'class': 'OTHER', 'fullName': 'University Health Network, Toronto'}, 'officialTitle': 'A Phase II, Open-Label, Randomized, Multi-Centre Study, of Neoadjuvant Olaparib in Patients With Platinum Sensitive Recurrent High Grade Serous Ovarian/Primary Peritoneal or Fallopian Tube Cancer', 'orgStudyIdInfo': {'id': 'OZM-058'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Olaparib Prior to Surgery, Chemotherapy/Olaparib Post Surgery', 'description': 'Olaparib, orally, at 300 mg twice per day, for 6 weeks (+/- 2 weeks) prior to surgery.\n\nPlatinum-based chemotherapy chosen by the study doctor and per standard of care after surgery.\n\nOlaparib, orally, at 300 mg twice per day, continuously, after chemotherapy.', 'interventionNames': ['Drug: Olaparib', 'Drug: Platinum-based Chemotherapy']}, {'type': 'EXPERIMENTAL', 'label': 'Olaparib Prior to Surgery and Post Surgery', 'description': 'Olaparib, orally, at 300 mg twice per day, for 6 weeks (+/- 2 weeks) prior to surgery and after surgery.', 'interventionNames': ['Drug: Olaparib']}], 'interventions': [{'name': 'Olaparib', 'type': 'DRUG', 'otherNames': ['Lynparza'], 'armGroupLabels': ['Olaparib Prior to Surgery and Post Surgery', 'Olaparib Prior to Surgery, Chemotherapy/Olaparib Post Surgery']}, {'name': 'Platinum-based Chemotherapy', 'type': 'DRUG', 'description': 'Chosen by the study doctor, per standard of care.', 'armGroupLabels': ['Olaparib Prior to Surgery, Chemotherapy/Olaparib Post Surgery']}]}, 'contactsLocationsModule': {'locations': [{'zip': 'T2N 4N2', 'city': 'Calgary', 'state': 'Alberta', 'country': 'Canada', 'facility': 'Tom Baker Cancer Centre', 'geoPoint': {'lat': 51.05011, 'lon': -114.08529}}, {'zip': 'K1H 8L6', 'city': 'Ottawa', 'state': 'Ontario', 'country': 'Canada', 'facility': 'Ottawa Regional Cancer Centre', 'geoPoint': {'lat': 45.41117, 'lon': -75.69812}}, {'zip': 'M5G 2M9', 'city': 'Toronto', 'state': 'Ontario', 'country': 'Canada', 'facility': 'Princess Margaret Cancer Centre', 'geoPoint': {'lat': 43.70643, 'lon': -79.39864}}, {'zip': 'H2L 2W5', 'city': 'Montreal', 'state': 'Quebec', 'country': 'Canada', 'facility': "Centre hospitalier de l'Université de Montréal (CHUM", 'geoPoint': {'lat': 45.50884, 'lon': -73.58781}}, {'zip': 'H3T 1E2', 'city': 'Montreal', 'state': 'Quebec', 'country': 'Canada', 'facility': 'Jewish General Hospital', 'geoPoint': {'lat': 45.50884, 'lon': -73.58781}}, {'city': 'Grafton', 'state': 'Auckland', 'country': 'New Zealand', 'facility': 'Auckland City Hospital', 'geoPoint': {'lat': -36.86029, 'lon': 174.76566}}, {'zip': '08035', 'city': 'Barcelona', 'country': 'Spain', 'facility': "Vall d'Hebron University Hospital", 'geoPoint': {'lat': 41.38879, 'lon': 2.15899}}, {'zip': 'SW3 6JJ', 'city': 'London', 'country': 'United Kingdom', 'facility': 'Royal Marsden Hospital NHS Foundation Trust', 'geoPoint': {'lat': 51.50853, 'lon': -0.12574}}, {'city': 'London', 'country': 'United Kingdom', 'facility': 'Imperial College Healthcare NHS Trust', 'geoPoint': {'lat': 51.50853, 'lon': -0.12574}}], 'overallOfficials': [{'name': 'Amit Oza, M.D.', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Princess Margaret Cancer Centre/University Health Network'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University Health Network, Toronto', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR'}}}}