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Spots Global Cancer Trial Database for Abemaciclib and Letrozole in Patients With Estrogen Receptor-positive Rare Ovarian Cancer

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Trial Identification

Brief Title: Abemaciclib and Letrozole in Patients With Estrogen Receptor-positive Rare Ovarian Cancer

Official Title: A Phase II, Open-label, Multicenter Study of Abemaciclib and Letrozole in Patients With Estrogen Receptor-positive Rare Ovarian Cancer

Study ID: NCT05872204

Study Description

Brief Summary: The purpose of this study is to assess the efficacy and safety of abemaciclib and letrozole for treatment of estrogen receptor-positive rare ovarian cancer.

Detailed Description: Patients with recurrent, persistent and/or metastatic estrogen receptor-positive rare ovarian cancer, who failed one line of platinum based chemotherapy for advanced or recurrent disease, will be included in this study. One cohort will include low-grade serous or endometrioid epithelial ovarian cancer and another cohort will include adult type granulosa cell tumors. The results of large randomized phase 3 trials of the combination of an aromatase inhibitor combined with a CDK4/6 inhibitor in hormone sensitive, HER2 negative breast cancer can form the basis for a trial with this drug combination in hormone sensitive rare ovarian cancer. The aim is to increase the response rate to aromatase inhibitors and the duration of response in this study population with limited therapeutic options, monitor the quality of life and explore the (epi)genomic signatures that correlate with response or endocrine resistance. Abemaciclib will be supplied as capsules administered orally, 150 mg every 12 hours (Q12H) on Days 1 to 28 of a 28-day cycle, plus letrozole 2.5 mg OD Days 1 to 28 of a 28-day cycle.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

UZ Gent, Gent, Oost-Vlaanderen, Belgium

UZ Leuven, Leuven, Vlaams-Brabant, Belgium

CHU de Liège, Liège, , Belgium

Institut De Cancerologie Strasbourg Europe, Strasbourg, Bas-Rhin, France

Institut Bergonie, Bordeaux, Gironde, France

Institut Universitaire Du Cancer Toulouse-Oncopole, Toulouse, Haute-Garonne, France

Institut De Cancerologie De L'Ouest, Saint-Herblain, Loire-Atlantique, France

Centre Leon Berard, Lyon, Métropole De Lyon, France

Groupe Hospitalier Diaconesses Croix Saint Simon, Paris, Île-de-France, France

Erasmus Medical Center Rotterdam, Rotterdam, South Holland, Netherlands

University Medical Center Groningen, Groningen, , Netherlands

University Medical Center Utrecht, Utrecht, , Netherlands

Contact Details

Name: Els Van Nieuwenhuysen, MD PhD

Affiliation: UZ Leuven

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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