| Titre |
An Open Label Randomized Phase 2 Trial of SAR439859, Versus Endocrine Monotherapy as Per Physician's Choice in Patients With Estrogen Receptor-positive, HER2-Negative Locally Advanced or Metastatic Breast Cancer With Prior Exposure to Hormonal Therapies |
| Protocole ID |
AMEERA-3 |
| ClinicalTrials.gov ID |
NCT04059484 |
| Type(s) de cancer |
Sein |
| Phase |
Phase II |
| Stade |
Maladie avancée ou métastatique |
| Type étude |
Traitement |
| Médicament |
SAR439859 |
| Institution |
CIUSSS DU CENTRE-OUEST-DE-L'ILE-DE-MONTREAL
 HOPITAL GENERAL JUIF SIR MORTIMER B.DAVIS
3755 rue de la Côte Ste. Catherine, Montréal, QC, H3T 1E2
|
| Ville |
Montréal |
| Investigateur(trice) principal(e) |
Dr Cristiano Ferrario
|
| Coordonnateur(trice) |
Heather Gregory
514-340-8222 poste 24596
|
| Statut |
![]() Fermé |
| Critètes d'éligibilité |
- 18 years or older
- Histological or cytological diagnosis of adenocarcinoma of the breast.
- Locally advanced not amenable to radiation therapy or surgery in a curative intent, and/or metastatic disease.
- ER positive status
- HER2 negative status
- For patients with tumor accessible for paired biopsy at study entry: baseline samples, formalin fixed paraffin embedded (FFPE) archived biopsy samples (within 3 months prior initiation of study treatment) can be used, but preferably fresh biopsies from primary tumor or recurrence or metastasis, will be collected.
- Participants must have received no more than 1 prior chemotherapeutic or 1 targeted therapy regimen for advanced/metastatic disease.
- Participants must have progressed after at least 6 months of a continuous prior endocrine therapy for advanced breast cancer
|
| Critètes d'exclusion |
- Eastern Cooperative Oncology Group performance status ≥2.
- Medical history or ongoing gastrointestinal disorders potentially affecting the absorption of SAR439859. Participants unable to swallow normally and to take capsules.
- Participant with any other cancer. Adequately treated basal cell or squamous cell skin cancer or in situ cervical cancer or any other cancer from which the participant has been disease free for >3 years are allowed.
- Severe uncontrolled systemic disease at screening .
- Participants with known brain metastases that are untreated, symptomatic or require therapy to control symptoms.
- Prior treatment with mammalian target of rapamycin inhibitors or any other selective estrogen receptor degrader (SERD) compound, except fulvestrant if stopped for at least3 months before randomization.
- Treatment with drugs that have the potential to inhibit UGT less than 2 weeks before randomization .
- Treatment with strong or moderate CYP3A/CYP2C8 inducers within 2 weeks before randomization.
- Ongoing treatment with drugs that are substrate of P-glycoprotein (P gp) (dabigatran, digoxin, fexofenadine).
- Treatment with anticancer agents (including investigational drugs) less than 3 weeks before randomization.
- Inadequate hematological, coagulation, renal and liver functions.
- The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
|
Groupe d'étude en oncologie du Québec