A Study Evaluating the Efficacy and Safety of GDC-9545 Combined With Palbociclib Compared With Letrozole Combined With Palbociclib in Participants With Estrogen Receptor-Positive, HER2-Negative Locally Advanced or Metastatic Breast Cancer

  • Cancer
  • Breast Cancer
  • Breast Cancer Er-Positive
  • Breast Cancer HER-2 Negative
  • Locally Advanced or Metastatic Breast Cancer
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:

Active, not recruiting

This trial runs in
Cities
  • Barrie
  • Brampton
  • Calgary
  • Montréal
  • Ottawa
  • Québec
  • Surrey
  • Toronto
Trial Identifier:

NCT04546009 2020-000119-66 BO41843

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      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

      Results Disclaimer

      Trial Summary

      This Phase III, randomized, double-blind, placebo-controlled, multicenter study will evaluate the efficacy and safety of giredestrant combined with palbociclib compared with letrozole combined with palbociclib in patients with estrogen receptor (ER)-positive, human epidermal growth factor receptor-2 (HER2)-negative locally advanced (recurrent or progressed) or metastatic breast cancer.

       

      We are able to provide travel reimbursement or travel services for patients located in remote locations or in areas that do not have trial locations. For more information about the trial, please contact Andrea Bickerton at andrea.bickerton@roche.com.

      Hoffmann-La Roche Sponsor
      Phase 3 Phase
      NCT04546009,BO41843,2020-000119-66 Trial Identifier
      Giredestrant, Giredestrant-matched Placebo, Letrozole, Letrozole-matched Placebo, Palbociclib, LHRH Agonist Treatments
      Estrogen Receptor-Positive, HER2-Negative Locally Advanced or Metastatic Breast Cancer Condition
      Official Title

      A Phase III Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Evaluating the Efficacy and Safety of GDC-9545 Combined With Palbociclib Compared With Letrozole Combined With Palbociclib in Patients With Estrogen Receptor-Positive, HER2-Negative Locally Advanced or Metastatic Breast Cancer

      Eligibility Criteria

      All Gender
      ≥18 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • For women who are premenopausal or perimenopausal and for men: treatment with approved LHRH agonist therapy for the duration of study treatment
      • Locally advanced (recurrent or progressed) or metastatic adenocarcinoma of the breast, not amenable to treatment with curative intent
      • Documented ER-positive tumor and HER2-negative tumor, assessed locally
      • Patients who have bilateral breast cancers which are both ER-positive and HER2-negative can be included in the study because the metastases are suitably targeted by the study treatments. If patients have bilateral tumors which are of different biomarker status, then proof of the ER and HER2 status of the metastases is required for study entry
      • No history of systemic anti-cancer therapy for locally advanced (recurrent or progressed) or metastatic disease
      • Disease recurrence from early-stage breast cancer after standard adjuvant endocrine therapy meeting the protocol-defined criteria of having received at least 24 months of treatment without disease progression during treatment and a disease-free interval since the completion of treatment that was greater than 12 months
      • Measurable disease as defined per RECIST v.1.1 or bone only disease which must have at least one predominantly lytic bone lesion confirmed by CT or MRI which can be followed
      • Eastern Cooperative Oncology Group Performance Status 0-1
      • Adequate organ function
      Exclusion Criteria
      • Disease recurrence during or within 12 months of completing prior neoadjuvant or adjuvant treatment with any CDK4/6 inhibitor
      • Prior treatment with a selective estrogen receptor degrader (SERD)
      • Treatment with any investigational therapy within 28 days prior to study treatment
      • Treatment with strong CYP3A inhibitors or inducers within 14 days or 5 drug elimination half-lives (whichever is longer) prior to randomization
      • Advanced, symptomatic, visceral spread that is at risk of life-threatening complications in the short term
      • Known active uncontrolled or symptomatic CNS metastases, carcinomatous meningitis, or leptomeningeal disease
      • Active cardiac disease or history of cardiac dysfunction, as defined in the protocol
      • Pregnant or breastfeeding

      For the latest version of this information please go to www.forpatients.roche.com

       

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