Breast Cancer Clinical Trial

Assessment of the Efficacy and Safety of Olaparib Monotherapy Versus Physicians Choice Chemotherapy in the Treatment of Metastatic Breast Cancer Patients With Germline BRCA1/2 Mutations.

Summary

This open label, randomised, controlled, multi-centre phase III study will assess the efficacy and safety of single agent olaparib vs standard of care based on physician's choice of capecitabine, vinorelbine or eribulin in metastatic breast cancer patients with gBRCA 1/2 mutations.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Germline mutation in BRCA1 or BRCA2 that is predicted to be deleterious or suspected deleterious.
Histologically or cytologically confirmed breast cancer with evidence of metastatic disease.
Prior therapy with an anthracycline and a taxane in either an adjuvant or metastatic setting.
Prior platinum allowed as long as no breast cancer progression occurred on treatment or if given in adjuvant/neoadjuvant setting at least 12 months from last dose to study entry elapsed.
ER/PR breast cancer positive patients must have received and progressed on at least one endocrine therapy (adjuvant or metastatic), or have disease that the treating physician believes to be inappropriate for endocrine therapy.
ECOG performance status 0-1.
Adequate bone marrow, kidney and liver function.

Exclusion Criteria:

Prior treatment with PARP inhibitor.
Patients with HER2 positive disease.
More than 2 prior lines of chemotherapy for metastatic breast cancer.
Untreated and/or uncontrolled brain metastases.
Prior malignancy unless curatively treated and disease-free for > 5 years prior to study entry. Prior adequately treated non-melanoma skin cancer, in situ cancer of the cervix, DCIS or stage I grade 1 endometrial cancer allowed.
Known HIV (Human Immunodeficiency Virus) infection.
Pregnant or breast-feeding women.

Study is for people with:

Breast Cancer

Phase:

Phase 3

Estimated Enrollment:

302

Study ID:

NCT02000622

Recruitment Status:

Active, not recruiting

Sponsor:

AstraZeneca

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There are 166 Locations for this study

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San Diego California, 92123, United States
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Santa Rosa California, 95403, United States
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Whittier California, 90602, United States
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Denver Colorado, 80204, United States
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New Haven Connecticut, 06510, United States
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Washington District of Columbia, 20007, United States
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Jacksonville Florida, 32224, United States
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Orlando Florida, 32804, United States
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Plantation Florida, 33324, United States
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Columbus Georgia, 31904, United States
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Marietta Georgia, 30060, United States
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Chicago Illinois, 60612, United States
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Niles Illinois, 60714, United States
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Wichita Kansas, 67214, United States
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Lafayette Louisiana, 70506, United States
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Boston Massachusetts, 02114, United States
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Boston Massachusetts, 02118, United States
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Boston Massachusetts, 02215, United States
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Detroit Michigan, 48201, United States
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Grand Rapids Michigan, 49503, United States
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Rochester Minnesota, 55905, United States
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Saint Louis Park Minnesota, 55416, United States
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Jackson Mississippi, 39202, United States
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Columbia Missouri, 65212, United States
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Saint Louis Missouri, 63131, United States
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Lebanon New Hampshire, 03756, United States
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Commack New York, 11725, United States
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Harrison New York, 10604, United States
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New York New York, 10021, United States
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New York New York, 10065, United States
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Rockville Centre New York, 11570, United States
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Syracuse New York, 13210, United States
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Cincinnati Ohio, 45267, United States
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Cleveland Ohio, 44106, United States
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Cleveland Ohio, 44195, United States
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Portland Oregon, 97213, United States
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Philadelphia Pennsylvania, 19104, United States
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Sayre Pennsylvania, 18840, United States
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Germantown Tennessee, 38138, United States
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Houston Texas, 77030, United States
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Tyler Texas, 75701, United States
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Burlington Vermont, 05401, United States
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Plovdiv , 4000, Bulgaria
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Plovdiv , 4004, Bulgaria
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Sofia , 1233, Bulgaria
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Sofia , 1303, Bulgaria
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Sofia , 1330, Bulgaria
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Sofia , 1504, Bulgaria
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Varna , 9010, Bulgaria
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Vratza , 3000, Bulgaria
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Beijing , 10000, China
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Beijing , 10002, China
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Beijing , 10014, China
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Changchun , 13006, China
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Changsha , 41001, China
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Chengdu , 61004, China
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Dalian , 11601, China
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Guangzhou , 51006, China
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Hangzhou , 31002, China
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Harbin , 15008, China
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Nanjing , 21000, China
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Shanghai , 20002, China
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Shanghai , 20003, China
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Shenyang , 11001, China
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Tianjin , 30006, China
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Brno , 656 5, Czechia
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Olomouc , 775 2, Czechia
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Praha 2 , 128 0, Czechia
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Caen Cedex , 14076, France
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Montpellier , 34298, France
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Rouen , 76038, France
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Strasbourg Cedex , 67065, France
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Villejuif , 94800, France
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Budapest , 1032, Hungary
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Budapest , 1083, Hungary
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Budapest , 1115, Hungary
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Budapest , 1122, Hungary
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Budapest , 1145, Hungary
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Nyíregyháza , 4400, Hungary
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Veszprém , 8200, Hungary
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Bologna , 40138, Italy
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Napoli , 80131, Italy
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Padova , 35128, Italy
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Roma , 00144, Italy
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Roma , 00168, Italy
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Rozzano , 20089, Italy
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Chuo-ku , 104-0, Japan
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Chuo-ku , 104-8, Japan
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Fukuoka-shi , 811-1, Japan
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Kagoshima-shi , 892-0, Japan
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Nagoya-shi , 464-8, Japan
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Osaka-city , 540-0, Japan
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Sapporo-shi , 003-0, Japan
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Shinagawa-ku , 142-8, Japan
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Suita-city , 565-0, Japan
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Cheongju-si , 28644, Korea, Republic of
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Daegu , 41404, Korea, Republic of
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Incheon , 21565, Korea, Republic of
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Seongnam-si , 13620, Korea, Republic of
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Seoul , 03080, Korea, Republic of
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Seoul , 03722, Korea, Republic of
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Seoul , 135-7, Korea, Republic of
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Seoul , 158-7, Korea, Republic of
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Estado de México , 50080, Mexico
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Merida , 97000, Mexico
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Merida , 97133, Mexico
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Mexico , 6760, Mexico
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Mérida , 97070, Mexico
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San Juan del Rio , 76800, Mexico
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Cusco , CUSCO, Peru
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Lima , LIMA , Peru
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Lima , Lima , Peru
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Lima , LIMA , Peru
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Lima , LIMA , Peru
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Lima , LIMA , Peru
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San Borja , LIMA , Peru
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ElblÄ…g , 82-30, Poland
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Gdańsk , 80-21, Poland
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Grzepnica , 72-00, Poland
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Tarnobrzeg , 39-40, Poland
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Warszawa , 01-74, Poland
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Warszawa , 03-29, Poland
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Łódź , 93-51, Poland
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Bucharest , 01381, Romania
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Bucuresti , 01117, Romania
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Bucuresti , 03017, Romania
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Cluj Napoca , 40001, Romania
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Cluj-Napoca , 40001, Romania
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Arkhangelsk , 16304, Russian Federation
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Ivanovo , 15304, Russian Federation
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Moscow , 11547, Russian Federation
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Omsk , 64401, Russian Federation
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Saint Petersburg , 19525, Russian Federation
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Saint Petersburg , 19527, Russian Federation
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Saint Petersburg , 19702, Russian Federation
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Saransk , 43000, Russian Federation
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St-Petersburg , 19775, Russian Federation
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St.Petersburg , 19101, Russian Federation
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Yaroslavl , 15005, Russian Federation
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Barcelona , 08003, Spain
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Córdoba , 14004, Spain
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Granada , 18014, Spain
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Madrid , 28034, Spain
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Majadahonda , 28222, Spain
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Oviedo , 33011, Spain
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Sevilla , 41013, Spain
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Valencia , 46026, Spain
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Zaragoza , 50009, Spain
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Bern , CH-30, Switzerland
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Lausanne , CH-10, Switzerland
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Zürich , 8055, Switzerland
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Kaohsiung , 80756, Taiwan
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Taichung , 407, Taiwan
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Taipei , 10048, Taiwan
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Taipei , 10449, Taiwan
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Taipei , 11217, Taiwan
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Taoyuan , 333, Taiwan
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Adana , 1260, Turkey
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Ankara , 06230, Turkey
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Edirne , 22030, Turkey
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Gaziantep , 27310, Turkey
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Istanbul , 34390, Turkey
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Izmir , 35100, Turkey
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Kayseri , 38039, Turkey
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Konya , 42080, Turkey
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Mersin , 33110, Turkey
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Aberdeen , AB25 , United Kingdom
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Colchester , CO4 5, United Kingdom
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Coventry , CV2 2, United Kingdom
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London , W6 8R, United Kingdom
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Manchester , M20 4, United Kingdom
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Plymouth , PL6 8, United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 3

Estimated Enrollment:

302

Study ID:

NCT02000622

Recruitment Status:

Active, not recruiting

Sponsor:


AstraZeneca

How clear is this clinincal trial information?

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