- Trials with a EudraCT protocol (213)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
213 result(s) found for: Letrozole.
Displaying page 1 of 11.
EudraCT Number: 2013-001219-57 | Sponsor Protocol Number: CLEE011X2107 | Start Date*: 2013-11-12 |
Sponsor Name:Novartis Farmacéutica, S.A. | ||
Full Title: A phase Ib/II, multicenter, study of the combination of LEE011 and BYL719 with letrozole in adult patients with advanced ER+ breast cancer | ||
Medical condition: advanced ER+ breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Temporarily Halted) IT (Completed) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002588-24 | Sponsor Protocol Number: CLEE011A2201 | Start Date*: 2013-12-30 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A randomized pre-surgical pharmacodynamics study to assess the biological activity of LEE011 plus letrozole versus single agent letrozole in primary breast cancer | ||
Medical condition: HR+, HER2- early breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) ES (Prematurely Ended) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001806-17 | Sponsor Protocol Number: AS1402-C-201 | Start Date*: 2008-11-17 | |||||||||||
Sponsor Name:Antisoma Research Limited | |||||||||||||
Full Title: A Phase II, Randomised, Open-Label, Multicentre Study of AS1402 in Combination with Letrozole as First Line Treatment in Postmenopausal Women with Locally Advanced or Metastatic Breast Cancer. | |||||||||||||
Medical condition: Locally Advanced or Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005067-33 | Sponsor Protocol Number: DBCG 07-REAL | Start Date*: 2009-02-09 |
Sponsor Name:DBCG | ||
Full Title: Randomized trial of endocrine therapy against locoregional therapy first. A DBCG trial in postmenopausal patients with operable hormone receptor positive tumors larger than 1 cm. | ||
Medical condition: Women age 60 or older with operable and hormone receptor positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004149-40 | Sponsor Protocol Number: PH2/053 | Start Date*: 2007-06-12 | |||||||||||
Sponsor Name:Cancer Research UK | |||||||||||||
Full Title: A Cancer Research UK randomised phase II trial of ATN-224 (copper binding agent) in combination with letrozole versus letrozole alone in post-menopausal women with recurrent, oestrogen and/or proge... | |||||||||||||
Medical condition: recurrent oestrogen and/or progesterone receptor positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001862-41 | Sponsor Protocol Number: CBYL719A2201 | Start Date*: 2013-11-26 |
Sponsor Name:Novartis Farmacéutica , S.A. | ||
Full Title: A phase II randomized, double-blind placebo controlled, study of letrozole with or without BYL719 or buparlisib, for the neoadjuvant treatment of postmenopausal women with hormone receptor-positive... | ||
Medical condition: neoadjuvant hormone-receptor positive HER2-negative breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) IT (Completed) AT (Completed) BE (Completed) DE (Completed) NL (Completed) CZ (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003065-17 | Sponsor Protocol Number: CRAD001Y24135 | Start Date*: 2013-05-16 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label, phase II, single-arm study of everolimus in combination with letrozole in the treatment of postmenopausal women with estrogen receptor positive HER2 negative metastatic or locally ad... | |||||||||||||
Medical condition: Estrogen receptor positive metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) FR (Completed) NL (Completed) PT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004601-27 | Sponsor Protocol Number: A5481008 | Start Date*: 2013-07-17 |
Sponsor Name:Pfizer Inc | ||
Full Title: A RANDOMIZED, MULTICENTER, DOUBLE-BLIND PHASE 3 STUDY OF PD-0332991 (ORAL CDK 4/6 INHIBITOR) PLUS LETROZOLE VERSUS PLACEBO PLUS LETROZOLE FOR THE TREATMENT OF POSTMENOPAUSAL WOMEN WITH ER (+), HER2... | ||
Medical condition: "Estrogen receptor-positive (ER+), HER2 negative (HER2-) Advanced Breast Cancer (ABC)" | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) BE (Completed) IE (Completed) FR (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) HU (Completed) IT (Completed) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006514-15 | Sponsor Protocol Number: RD-5103-015-06 | Start Date*: 2007-11-26 | |||||||||||
Sponsor Name:The University of Nottingham [...] | |||||||||||||
Full Title: Double blind crossover randomised controlled trial comparing letrozole versus clomifene citrate for ovulation induction in women with polycystic ovarian syndrome | |||||||||||||
Medical condition: Infertility due to polycycstic ovarian syndrome | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003044-53 | Sponsor Protocol Number: B1271003 | Start Date*: 2012-01-30 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 US | |||||||||||||
Full Title: AN OPEN-LABEL, RANDOMISED PHASE 1B/2 STUDY OF PF-04691502 IN COMBINATION WITH LETROZOLE COMPARED WITH LETROZOLE ALONE IN PATIENTS WITH ESTROGEN RECEPTOR POSITIVE, HER-2 NEGATIVE EARLY BREAST CANCER | |||||||||||||
Medical condition: ESTROGEN RECEPTOR POSITIVE, HER-2 NEGATIVE EARLY BREAST CANCER WITH KI-67 HIGHER THAN 10% AND ESTROGEN RECEPTOR POSITIVE, HER-2 NEGATIVE ADVANCED BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Prematurely Ended) SE (Prematurely Ended) ES (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003752-79 | Sponsor Protocol Number: PIONEER | Start Date*: 2017-05-24 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | |||||||||||||
Full Title: Randomised Phase II clinical trial PIONEER- A Pre-operative wIndOw study of letrozole plus PR agonist (Megestrol Acetate) versus letrozole aloNE in post-menopausal patients with ER-positive breast ... | |||||||||||||
Medical condition: ER-positive, HER2-negative, invasive primary breast cancer of at least 1 cm size | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002304-33 | Sponsor Protocol Number: no sponsor | Start Date*: 2006-09-12 | |||||||||||
Sponsor Name:Rijnstate Hospital | |||||||||||||
Full Title: Letrozole Treatment to Normalize Serum Testosterone in Men with Hypogonadotropic Hypogonadism due to Pituitary Damage. | |||||||||||||
Medical condition: Hypogonadotropic hypogonadism in men with pituitary damage other than irradiation | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004266-40 | Sponsor Protocol Number: ICORG 06-32/NSABP B-42 | Start Date*: 2007-11-02 |
Sponsor Name:ICORG | ||
Full Title: A Clinical Trial to Determine the Efficacy of Five Years of Letrozole Compared to Placebo in Patients Completing Five Years of Hormonal Therapy Consisting of an Aromatase Inhibitor (AI) or Tamoxife... | ||
Medical condition: Hormone Receptor Positive Breast Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000454-32 | Sponsor Protocol Number: C/23/2011 | Start Date*: 2012-01-17 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A single arm phase IIa study (with combination safety run-in) to assess the safety and efficacy of AZD4547 in combination with either anastrozole or letrozole in ER positive breast cancer patients ... | |||||||||||||
Medical condition: ER Positive Progressing Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000568-28 | Sponsor Protocol Number: GO28888 | Start Date*: 2014-10-16 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A phase II randomized, double-blind study of neoadjuvant letrozole plus GDC-0032 versus letrozole plus placebo in postmenopausal women with ER-positive/HER2-negative, early stage breast cancer | |||||||||||||
Medical condition: WOMEN WITH ER-POSITIVE/HER2-NEGATIVE, EARLY STAGE BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) AT (Completed) CZ (Completed) PT (Completed) HU (Completed) IT (Completed) GB (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000887-16 | Sponsor Protocol Number: ICR-CTSU/2014/10044 | Start Date*: 2014-11-07 | |||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust [...] | |||||||||||||
Full Title: A phase II randomised study evaluating the biological and clinical effects of the combination of palbociclib with letrozole as neoadjuvant therapy in post-menopausal women with ER+ primary breast c... | |||||||||||||
Medical condition: ER positive, HER2 negative early invasive breast cancer | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002192-18 | Sponsor Protocol Number: TRIO020 | Start Date*: 2013-10-17 |
Sponsor Name:Translational Research In Oncology | ||
Full Title: A randomized open-label Phase II study of letrozole plus afatinib (BIBW2992) versus letrozole alone in first-line treatment of advanced ER+, HER2- postmenopausal breast cancer with low ER expression | ||
Medical condition: Advanced ER+, HER2- postmenopausal breast cancer with low ER expression | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003467-19 | Sponsor Protocol Number: CLEE011A2404 | Start Date*: 2016-12-08 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: COMPLEEMENT-1: An open-label, multicenter, Phase IIIb study to assess the safety and efficacy of ribociclib (LEE011) in combination with letrozole for the treatment of men and pre/postmenopausal wo... | |||||||||||||
Medical condition: hormone receptor-positive (HR+) HER2-negative (HER2-) advanced breast cancer (aBC) with no prior hormonal therapy for advanced disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) HU (Completed) BG (Completed) PT (Completed) GR (Completed) SK (Completed) IT (Completed) CZ (Completed) AT (Completed) ES (Completed) DK (Completed) NO (Completed) PL (Completed) FI (Completed) SI (Completed) RO (Ongoing) LU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000676-29 | Sponsor Protocol Number: BOOG-2017-01 | Start Date*: 2018-01-12 | |||||||||||
Sponsor Name:BOOG Study Center | |||||||||||||
Full Title: Tailoring neoadjuvant therapy in hormone receptor positive, HER2 negative, luminal breast cancer. | |||||||||||||
Medical condition: Mamma carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002418-12 | Sponsor Protocol Number: CFEM345D2407 | Start Date*: 2005-01-25 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An open-label, randomized, multicenter safety study to evaluate the skeletal and lipid profile effects of letrozole and tamoxifen in postmenopausal women with resected, receptor positive early brea... | ||
Medical condition: Bone loss attributed to cessation of ovarian estrogen production is common in postmenopausal women. In postmenopausal women with breast cancer, treatment with an aromatase inhibitor may further red... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) GB (Completed) | ||
Trial results: View results |
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