Breast Cancer Clinical Trial

A Study of Giredestrant (GDC-9545) in Postmenopausal Women With Stage I-III Operable, Estrogen Receptor-Positive Breast Cancer

Summary

This study will evaluate the pharmacodynamics, pharmacokinetics, safety, and biologic activity of giredestrant in participants with Stage I-III operable estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative, untreated breast cancer.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Ability to comply with the study protocol, in the investigator's judgment
Histologically confirmed invasive breast carcinoma, with all of the following characteristics: Primary tumor greater than or equal to (≥)1.5 centimeters (cm) in largest diameter by ultrasound; Stage I-III operable breast cancer; Documentation confirming the absence of distant metastasis (M0) as determined by institutional practice.
ER-positive tumor and HER2-negative breast cancer as per local laboratory testing
Postmenopausal status
Breast cancer eligible for primary surgery
Submission of a representative tumor tissue specimen
Eastern Cooperative Oncology Group (ECOG) Performance Status less than or equal to (≤)1
Adequate organ function

Exclusion Criteria:

Diagnosis of inflammatory breast cancer
Diagnosis of bilateral breast cancer
Concurrent use of hormone replacement therapies
Previous systemic or local treatment for the primary breast cancer currently under investigation
Concurrent treatment with other experimental drugs or participation in another clinical trial with any investigational drug within 30 days prior to study entry
Current treatment with any systemic anti-cancer therapies
Major surgery within 4 weeks prior to enrollment
Radiation therapy within 2 weeks prior to enrollment
Diagnosis of any secondary malignancy within 3 years prior to enrollment, except for appropriately treated carcinoma in situ of the cervix, non-melanoma skin carcinoma, or Stage I uterine cancer
Active inflammatory bowel disease or chronic diarrhea, short bowel syndrome, or upper gastrointestinal surgery including gastric resection
Known HIV infection
Known clinically significant history of liver disease consistent with Child-Pugh Class B or C, including active viral or other hepatitis, current alcohol abuse, or cirrhosis
Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study
History of allergy to giredestrant or any of its excipients
Any condition requiring anti-coagulants, such as warfarin, heparin, or thrombolytic drugs
History of documented hemorrhagic diathesis or coagulopathy
History or presence of symptomatic bradycardia or sick sinus syndrome
Baseline heart rate ≤55 beats per minute (bpm) prior to enrollment
History or presence of an abnormal electrocardiogram (ECG) that is clinically significant in the investigator's opinion, including complete left bundle branch block, second- or third-degree heart block, or evidence of prior myocardial infarction
QT interval corrected through use of Fridericia's formula (QTcF) >470 milliseconds demonstrated by at least two ECGs >30 minutes apart
History of ventricular dysrhythmias or risk factors for ventricular dysrhythmias such as structural heart disease, coronary heart disease, clinically significant electrolyte abnormalities, or family history of sudden unexplained death or long QT syndrome
Current treatment with medications that are well known to prolong the QT interval
History or presence of uncontrolled hypothyroidism
Any other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding that, in the investigator's opinion, gives reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect the interpretation of the results or render the patient at high risk from treatment complications

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

75

Study ID:

NCT03916744

Recruitment Status:

Completed

Sponsor:

Genentech, Inc.

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There are 15 Locations for this study

See Locations Near You

University of Colorado
Aurora Colorado, 80045, United States
Massachusetts General Hospital
Boston Massachusetts, 02114, United States
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States
St Vincent's Hospital Sydney
Darlinghurst New South Wales, 2010, Australia
Sunshine Hospital
St Albans Victoria, 3021, Australia
Clinique Edith Cavell; Pharmacie
Auderghem , 1160, Belgium
UZ Antwerpen
Edegem , 2650, Belgium
Clinique Sainte-Elisabeth; Oncologie
Namur , 5000, Belgium
Onkologikoa - Instituto Oncológico de Donostia
San Sebastian Guipuzcoa, 20014, Spain
Hospital Universitari Vall d'Hebron
Barcelona , 08035, Spain
Hospital Ruber Internacional;Servicio de Oncologia
Madrid , 28034, Spain
HM Sanchinarro ? CIOCC
Madrid , 28050, Spain
Hospital Clinico Universitario de Valencia
Valencia , 46010, Spain
Barts Health NHS Trust; William Harvey Heart Centre, QMUL School of Medicine & Dentistry
London , EC1M , United Kingdom
Royal Cornwall Hospital
Truro , TR1 3, United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

75

Study ID:

NCT03916744

Recruitment Status:

Completed

Sponsor:


Genentech, Inc.

How clear is this clinincal trial information?

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