Phase 1/2 Study of Amcenestrant (SAR439859) Single Agent and in Combination With Other Anti-cancer Therapies in Postmenopausal Women With Estrogen Receptor Positive Advanced Breast Cancer (AMEERA-1)

A Phase 1/2 Study for the Safety, Efficacy, Pharmacokinetic and Pharmacodynamics Evaluation of Amcenestrant (SAR439859), Administered Orally as Monotherapy, Then in Combination With Other Anti-cancer Therapies in Postmenopausal Women With Estrogen Receptor-positive Advanced Breast Cancer

Primary Objectives:

Dose Escalation:

• To assess the incidence rate of dose-limiting toxicity (DLT) and to determine the maximum tolerated dose (MTD) as well as the recommended dose (RD) of amcenestrant administered as monotherapy and in combination with palbociclib
• To assess the incidence rate of DLT and determine the RD of everolimus or abemaciclib in combination with the selected amcenestrant dose for the combination therapy

Safety Run-In:

- To confirm the RD of amcenestrant in combination with alpelisib

Dose Expansion:

• Antitumor activity using objective response rate (ORR)
• Overall safety profile of amcenestrant administered in combination with palbociclib, alpelisib, everolimus, and abemaciclib

Secondary Objectives:

• Overall safety profile of amcenestrant monotherapy and in combination
• Pharmacokinetic (PK) profile of amcenestrant administered as monotherapy or in combination and PK profile of palbociclib, alpelisib, everolimus and abemaciclib
• Antitumor activity using ORR, the clinical benefit rate (CBR) and progression free survival (PFS)
• Time to first tumor response
• Residual ER availability with positron emission tomography (PET) scan [(18)F] fluoroestradiol (18F-FES) uptake with increasing doses of amcenestrant
• Food effect on PK of amcenestrant
• Potential induction/inhibition effect of amcenestrant on cytochrome P450 (CYP) 3A using 4b-OH cholesterol

Study Overview

• Status: Active, not recruiting
• Conditions: Breast Cancer
• Intervention / Treatment: Drug: Amcenestrant; Drug: Palbociclib; Drug: Alpelisib; Drug: Everolimus; Drug: Abemaciclib

Detailed Description

Duration of the study, per participant, will include eligibility period (screening period) of up to 4 weeks (28 days), treatment period (at least 1 cycle [28 days] of study treatment), and end of treatment (EOT) visit at least 22 to 30 days (or until the participant receives another anticancer therapy, whichever is earlier) following the last study treatment administration. The expected enrollment period is approximately 60 months.

• Study Type: Interventional
• Enrollment (Actual): 136
• Phase: Phase 2; Phase 1

Contacts and Locations

Study Locations

• Belgium
  • Leuven, Belgium, 3000
    • Investigational Site Number : 0560001
• Canada
  • Alberta
    • Edmonton, Alberta, Canada, T6G 1Z2
      • Investigational Site Number : 1240004
  • British Columbia
    • Vancouver, British Columbia, Canada, V5Z 4E6
      • Investigational Site Number : 1240003
  • Ontario
    • Toronto, Ontario, Canada, M4N 3M5
      • Investigational Site Number : 1240002
• Czechia
  • Brno, Czechia, 65653
    • Investigational Site Number : 2030002
  • Praha 2, Czechia, 12808
    • Investigational Site Number : 2030001
  • Praha 4, Czechia, 14059
    • Investigational Site Number : 2030003
• France
  • Bordeaux Cedex, France, 33076
    • Investigational Site Number : 2500002
  • Lille, France, 59020
    • Investigational Site Number : 2500005
  • Lyon, France, 69373
    • Investigational Site Number : 2500003
  • Saint-Herblain, France, 44805
    • Investigational Site Number : 2500001
  • Villejuif, France, 94800
    • Investigational Site Number : 2500004
• Italy
  • Milano, Italy, 20141
    • Investigational Site Number : 3800003
• Poland
  • Pomorskie
    • Gdynia, Pomorskie, Poland, 81-519
      • Investigational Site Number : 6160004
• Portugal
  • Lisboa, Portugal, 1649-035
    • Investigational Site Number : 6200001
  • Lisboa, Portugal, 1998-018
    • Investigational Site Number : 6200002
• Spain
  • Madrid, Spain, 28041
    • Investigational Site Number : 7240001
  • Madrid, Comunidad De
    • Madrid, Madrid, Comunidad De, Spain, 28034
      • Investigational Site Number : 7240007
    • Madrid, Madrid, Comunidad De, Spain, 28050
      • Investigational Site Number : 7240002
• United Kingdom
  • Oxfordshire
    • Oxford, Oxfordshire, United Kingdom, OX3 7LE
      • Investigational Site Number : 8260003
  • Vale Of Glamorgan, The
    • Cardiff, Vale Of Glamorgan, The, United Kingdom, CF14 2TL
      • Investigational Site Number : 8260002
• United States
  • Colorado
    • Denver, Colorado, United States, 80262
      • University of Colorado Site Number : 8400005
  • Massachusetts
    • Boston, Massachusetts, United States, 02114
      • Massachusetts General Hospital Site Number : 8400002
  • New York
    • New York, New York, United States, 10065
      • Memorial Sloan Kettering Cancer Center Site Number : 8400003
  • Washington
    • Seattle, Washington, United States, 98109
      • Seattle Cancer Care Alliance Site Number : 8400001

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion criteria:

• Participants must be postmenopausal women
• Histological diagnosis of breast adenocarcinoma
• Locally advanced or metastatic disease
• Either primary tumor or any metastatic site to be positive for Estrogen Receptors (ER+) and negative for HER2 (HER2-) receptor
• Participants must have been previously treated with at least 6 months of endocrine therapy for advanced disease:
• Dose Escalation study parts:

Arm #3 - Part F and Arm #5 - Part J: up to 2 prior lines of either single endocrine therapy and/or endocrine-based therapy Arm #4 -H: up to 2 prior lines of either single endocrine therapy and/or endocrine-based therapy (exemestane not allowed)

- Dose Expansion study parts: Arm #2: - Part D: no more than 2 prior lines of advanced endocrine therapy for advanced disease are allowed Arm #3, - Part G: patients must have received and progressed on the combination of Aromatase Inhibitors (AI) + CDK4/6 inhibitor as the first line (1L) treatment for advanced disease Arm #4 - Part I: participants must have received and progressed on the combination of Aromatase Inhibitors (AI) +CDK4/6 Inhibitor as the first line (1L) treatment for advanced disease (exemestane not allowed) Arm#5: - Part K: up to 1 prior line of a single endocrine therapy for advanced disease Note: Additional patients who relapsed while on previous adjuvant endocrine therapy that was initiated ≥24 months ago, or relapsed < 12 months after completion of adjuvant endocrine therapy are also allowed for Arms #2, #3, #4, and #5 (Parts C, D, F, G, H, I, J and K).

• Participants previously treated with chemotherapy for advanced disease: no more than 3 prior chemotherapeutic regimens in Arm #1 Part A, and no more than 1 prior chemotherapeutic regimen in Arms #1, #2, #3, #4, and #5 (Parts B, C, D, F, H and J respectively); prior chemotherapy for advanced disease is not allowed in dose expansion of Arms #3, #4, and #5 (Part G, I and K respectively).
• Measurable lesion

Exclusion criteria:

• Medical history or ongoing gastrointestinal disorders that could affect absorption of oral study drugs (including difficulties with swallowing capsules)
• Participants with any other cancer (except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer or any other cancer from which the participant has been disease free for >3 years)
• Participants with known brain metastases
• Treatment with anticancer agents (including investigational drugs) less than 2 weeks before first study treatment starts (less than 4 weeks if the anticancer agents were antibodies)
• Prior treatment with another selective ER down-regulator (SERD)
• Dose Escalation study parts (Parts F, H and J): SERDs are not allowed except for fulvestrant which will need a washout of at least 6 weeks prior to the first study drug administration
• Dose Expansion study parts (Parts G, I and K): prior (last) treatment with any SERD including fulvestrant will not be allowed
• Inadequate hematological and biochemical lab tests
• Participants with Gilbert disease
• Treatment with HIV-antiviral, antifungal and antioxidant agents less than 2 weeks before study treatment starts
• Treatment with strong P450 (CYP) 3A inducers within 2 weeks before first study treatment
• Treatment with OATP1B1/B3 sensitive substrates and which cannot be replaced
• Arm#2 Treatment with strong CYP3A inhibitors within 2 weeks before first study treatment starts
• More than one prior advanced cyclin-dependent kinase (CDK) 4/6 inhibitor-based therapy in Arm #1, Arm #2 (Part C), Arm #3 (Parts F and G), and Arm#4 (Part H).
• Arm #2, #3, #4 and #5 (Parts C, D, F, G, H, I, J and K) only: participants with concurrent or history of pneumonitis
• Arm #3, #4 and #5 (Parts F, G, H, I, J and K) only: prior treatment therapies that target the PI3K axis (mTOR inhibitors, AKT inhibitors, PI3K inhibitors)
• Arm #3 and #4 (Parts F, G, H and I) only: participants with diabetes mellitus type-I or uncontrolled diabetes mellitus type-II: ie, fasting plasma glucose ≥ 140mg/dl (7.7 mmol/l) or HbA1C > 6.2%
• Arm #3 and #4 (Parts F, G, H and I) only: history of severe cutaneous reaction (eg. Stevens-Johnson syndrome [SJS], erythema multiforme [EM]), toxic epidermal necrolysis (TEN), and drug reaction with eosinophilia and systemic symptoms [DRESS].
• Arm #3 (Parts F and G) only: ongoing osteonecrosis of jaw
• Arm #4 (Parts H and I) only: any active, untreated or uncontrolled infection (e.g. viral, bacterial, fungal etc.)
• Arm #4 (Parts H and I) only: participants with active and uncontrolled stomatitis, angioedema due to concomitant treatment with ACE inhibitors, impaired wounds
• Arm #4 (Parts H and I) only: uncontrolled hypercholesterolemia, hypertriglyceridemia and hyperglycemia in non-diabetic participants
• Arm #4 (Parts H and I) only: treatment with strong or moderate CYP3A4 inhibitors, strong CYP3A4 inducers and/or P-gp inhibitors within 2 weeks before the first study treatment administration or 5 elimination half-lives, whichever is the longest
• Arm #5 (Parts J and K) only: history or current (controlled/not controlled) venous thromboembolism (i.e. deep vein thrombosis (DVT), pulmonary embolism (PE), cerebral venous sinus thrombosis (CVST)

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

5

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Amcenestrant Monotherapy: Arm #1 Part A Dose Escalation, Part B Dose Expansion; Part A: Amcenestrant will be administered orally once daily (QD). Treatment will begin with an identified starting dose. Administration of higher doses to subsequent participants is based on occurrence of DLTs and evaluation of target saturation and PK parameters at initial and subsequent doses, until maximum administered dose (MAD) is reached. Drug will be administered in a 28-day cycle. Part B: When the dose escalation phase ends, the recommended dose will be administered for the expansion cohort. Drug will be administered in a 28-day cycle.	Drug: Amcenestrant; Pharmaceutical form: capsule Route of administration: oral; Other Names: SAR439859
Experimental: Amcenestrant/Palbociclib: Arm #2 Part C Dose Escalation, Part D Dose Expansion; Part C: Amcenestrant will be administered in combination with palbociclib: amcenestrant starting oral daily dose will be one dose level below monotherapy RD and palbociclib will be dosed at fixed standard dose. Administration of higher dose of amcenestrant (with standard palbociclib dose) to subsequent participants will be based on occurrence of DLTs at initial and subsequent doses, until MAD of amcenestrant is reached. Drugs will be administered in a 28-day cycle (palbociclib will be administered for 21 days of cycle). Part D: Based on the results in Part C, participants will be administered either: 1) a determined amcenestrant dose (RD) with standard dose of palbociclib in combination therapy, or 2) one of two randomized dose levels of amcenestrant with standard dose of palbociclib in combination therapy. Drugs will be administered in a 28-day cycle (palbociclib will be administered for 21 days of cycle).	Drug: Amcenestrant; Pharmaceutical form: capsule Route of administration: oral; Other Names: SAR439859; Drug: Palbociclib; Pharmaceutical form: capsule Route of administration: oral; Other Names: Ibrance®
Experimental: Amcenestrant/Alpelisib: Arm #3 Part F Safety Run-In, Part G Dose Expansion; Part F: Amcenestrant will be administered in combination with alpelisib at a fixed standard dose. Additional dose levels of amcenestrant with alpelisib could be explored if needed based on the safety and PK results. Lower dose of alpelisib could be explored based on the PK results and safety profile from the initial combination administration. Both amcenestrant and alpelisib will be administered in a 28-day cycle. Part G: Based on the conclusion in Part F, participants will be administered the determined RD of amcenestrant and alpelisib given in the combination in an expansion cohort. Both study drugs will be administered in a 28-day cycle.	Drug: Amcenestrant; Pharmaceutical form: capsule Route of administration: oral; Other Names: SAR439859; Drug: Alpelisib; Pharmaceutical form: tablet Route of administration: oral; Other Names: Piqray®
Experimental: Amcenestrant/Everolimus: Arm #4 Part H Dose Escalation, Part I Dose Expansion; Part H: Amcenestrant will be administered at the determined RD in combination with 2 dose levels of everolimus. Additional dose levels of amcenestrant with everolimus could be explored if needed based on the safety and PK results. Both amcenestrant and everolimus will be administered in a 28-day cycle. Part I: Based on the conclusion in Part H, participants will be administered the determined RD of amcenestrant and RD of everolimus given in the combination in an expansion cohort. Both study drugs will be administered in a 28-day cycle.	Drug: Amcenestrant; Pharmaceutical form: capsule Route of administration: oral; Other Names: SAR439859; Drug: Everolimus; Pharmaceutical form: tablet
Experimental: Amcenestrant/Abemaciclib: Arm #5 Part J Dose Escalation, Part K Dose Expansion; Part J: Amcenestrant will be administered at the determined RD in combination with 2 dose levels of abemaciclib. Additional dose levels of amcenestrant with abemaciclib could be explored if needed based on the safety and PK results. Both amcenestrant and abemaciclib will be administered in a 28-day cycle. Part K: Based on the conclusion in Part J, participants will be administered the determined RD of amcenestrant and RD of abemaciclib given in the combination in an expansion cohort. Both study drugs will be administered in a 28-day cycle.	Drug: Amcenestrant; Pharmaceutical form: capsule Route of administration: oral; Other Names: SAR439859; Drug: Abemaciclib; Pharmaceutical form: tablet; Other Names: Verzenio®

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Dose Limiting Toxicities (DLTs)	Incidence of study treatment-related DLTs at Cycle 1 (Arm #1 Part A, Arm #2 Part C, Arm #3 Part D, Arm #4 Part H, and Arm #5 Part J)	Cycle 1, Day 28 for each treated participant (each cycle is 28 days)
Objective Response Rate (ORR)	Proportion of participants with confirmed CR or PR according to RECIST 1.1 assessed by independent central reviewer relative to the total number of treated participants (Arm #1 Part B)	Baseline to date of first documentation of progression, assessed up to approximately 6 months after the last entered participant
Adverse Events	Number of participants with adverse events according to the National Cancer Institute - Common Toxicity Criteria (NCI-CTC) version 4.03 grade scaling; incidence of adverse events, including laboratory test results and electrocardiogram (ECG) findings that were adverse events (Arm #2 Part D, Arm #3 Part G, Arm #4 Part I, Arm #5 Part K)	Up to 30 days after last dose of amcenestrant

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Adverse Events	Number of participants with adverse events according to the National Cancer Institute - Common Toxicity Criteria (NCI-CTC) version 4.03 grade scaling; incidence of adverse events, including laboratory test results and electrocardiogram (ECG) findings that were adverse events in all treatment arms	Up to 30 days after last dose of amcenestrant
ORR	Proportion of participants with complete response (CR) or partial response (PR) according to RECIST 1.1 assessed by investigator/local radiologist relative to the total number of treated participants in all treatment arms	Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant
Time to First Response (TTR)	Time from the start of treatment to the first objective tumor response observed for participants who achieved CR or PR in all treatment arms	Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant
Clinical Benefit Rate (CBR)	Proportion of participants with CR or PR or SD ≥24 weeks according to RECIST v.1.1 relative to the total number of treated participants by investigators/local radiologists in all treatment arms and by independent central reviewer in Arm #1 Part B	Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant
Duration of response	Time from initial response to the first documented tumor progression in all treatment arms	Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant
tlag of amcenestrant after single dose	tlag is interval between administration time and the sampling time preceding the first concentration above the lower limit of quantification of amcenestrant (Arms #1, #2, #4, and #5)	Cycle 1, Day 1 and Day 3 (each cycle is 28 days)
tmax of amcenestrant after single dose	tmax is time to reach Cmax (Arms #1, #2, #4, and #5)	Cycle 1, Day 1 and Day 3 (each cycle is 28 days)
Cmax of amcenestrant after single dose	Cmax is maximum concentration observed (Arms #1, #2, #4, and #5)	Cycle 1, Day 1 and Day 3 (each cycle is 28 days)
AUC0-24 of amcenestrant after single dose	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arms #1, #2, #4, and #5)	Cycle 1, Day 1 and Day 3 (each cycle is 28 days)
tmax of amcenestrant after repeated dose administration	tmax is time to reach Cmax in all treatment arms	Cycle 1, Day 21 or 22 (each cycle is 28 days)
Cmax of amcenestrant after repeated dose administration	Cmax is maximum concentration observed in all treatment arms	Cycle 1, Day 21 or 22 (each cycle is 28 days)
AUC0-24 of amcenestrant after repeated dose administration	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) in all treatment arms	Cycle 1, Day 21 or 22 (each cycle is 28 days)
Ctrough of amcenestrant during repeated dose administration	Ctrough is plasma concentration observed just before treatment administration during repeated dosing in all treatment arms	Cycle 1, Day 8, Day 21 or 22 and Cycle 2, Day 1 (each cycle is 28 days)
tmax of palbociclib after single dose	tmax is time to reach Cmax (Arm #2)	Cycle 1, Day 1 (each cycle is 28 days)
Cmax of palbociclib after single dose	Cmax is maximum concentration observed (Arm #2)	Cycle 1, Day 1 (each cycle is 28 days)
AUC0-24 of palbociclib after single dose	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #2)	Cycle 1, Day 1 (each cycle is 28 days)
tmax of palbociclib after repeated dose administration	tmax is time to reach Cmax (Arm #2)	Cycle 1, Day 21 (each cycle is 28 days)
Cmax of palbociclib after repeated dose administration	Cmax is maximum concentration observed (Arm #2)	Cycle 1, Day 21 (each cycle is 28 days)
AUC0-24 of palbociclib after repeated dose administration	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #2)	Cycle 1, Day 21 (each cycle is 28 days)
Urine excretion of amcenestrant	Urine excretion of amcenestrant during the monotherapy expansion phase (Arm #1 Part B)	Cycle 1, Day 21 (each cycle is 28 days)
Cholesterol concentration ratios	Plasma 4B hydroxy/total cholesterol concentration ratios (Arm #1)	Up to Cycle 2 (each cycle is 28 days)
ER occupancy at 18F-FES-PET imaging	Inhibition of ER occupancy at 18F-FES-PET imaging (signal extinction) (Arm #1 Part A)	Baseline and one assessment in Cycle 1 on Day 11 to 15 (each cycle is 28 days)
Progression free survival	Time interval from the date of the first IMP intake to the date of the first tumor progression assessed by investigators/local radiologists in all treatment arms and (also by IRC in Part B) per RECIST 1.1, or death (due to any cause), whichever comes first.	Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant
Observation of tumor changes by FES PET and FDG PET scans	To correlate the changes observed in FES PET scan with the changes in glucose metabolism seen on FDG PET (Arm #1 Part A)	Baseline and approximately at Day 15 of Cycle 1 in Part A (each cycle is 28 days)
tmax of alpelisib after third dose	tmax is time to reach Cmax (Arm #3)	Cycle 1, Day 3 (each cycle is 28 days)
Cmax of alpelisib after third dose	Cmax is maximum concentration observed (Arm #3)	Cycle 1, Day 3 (each cycle is 28 days)
AUC0-24 of alpelisib after third dose	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #3)	Cycle 1, Day 3 (each cycle is 28 days)
tmax of alpelisib after repeated dose administration	tmax is time to reach Cmax (Arm #3)	Cycle 1, Day 22 (each cycle is 28 days)
Cmax of alpelisib after repeated dose administration	Cmax is maximum concentration observed (Arm #3)	Cycle 1, Day 22 (each cycle is 28 days)
AUC0-24 of alpelisib after repeated dose administration	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #3)	Cycle 1, Day 22 (each cycle is 28 days)
tmax of everolimus after single dose	tmax is time to reach Cmax (Arm #4)	Cycle 1, Day 1 (each cycle is 28 days)
Cmax of everolimus after single dose	Cmax is maximum concentration observed (Arm #4)	Cycle 1, Day 1 (each cycle is 28 days)
AUC0-24 of everolimus after single dose	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #4)	Cycle 1, Day 1 (each cycle is 28 days)
tmax of everolimus after repeated dose administration	tmax is time to reach Cmax (Arm #4)	Cycle 1, Day 22 (each cycle is 28 days)
Cmax of everolimus after repeated dose administration	Cmax is maximum concentration observed (Arm #4)	Cycle 1, Day 22 (each cycle is 28 days)
AUC0-24 of everolimus after repeated dose administration	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #4)	Cycle 1, Day 22 (each cycle is 28 days)
tmax of abemaciclib after single dose	tmax is time to reach Cmax (Arm #5)	Cycle 1, Day 1 (each cycle is 28 days)
Cmax of abemaciclib after single dose	Cmax is maximum concentration observed (Arm #5)	Cycle 1, Day 1 (each cycle is 28 days)
AUC0-24 of abemaciclib after single dose	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #5)	Cycle 1, Day 1 (each cycle is 28 days)
tmax of abemaciclib after repeated dose administration	tmax is time to reach Cmax (Arm #5)	Cycle 1, Day 22 (each cycle is 28 days)
Cmax of abemaciclib after repeated dose administration	Cmax is maximum concentration observed (Arm #5)	Cycle 1, Day 22 (each cycle is 28 days)
AUC0-24 of abemaciclib after repeated dose administration	AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #5)	Cycle 1, Day 22 (each cycle is 28 days)

Collaborators and Investigators

• Sponsor: Sanofi
• Investigators: Study Director: Clinical Sciences & Operations, Sanofi

Publications and helpful links

General Publications

• Bardia A, Chandarlapaty S, Linden HM, Ulaner GA, Gosselin A, Cartot-Cotton S, Cohen P, Doroumian S, Paux G, Celanovic M, Pelekanou V, Ming JE, Ternes N, Bouaboula M, Lee JS, Bauchet AL, Campone M. AMEERA-1 phase 1/2 study of amcenestrant, SAR439859, in postmenopausal women with ER-positive/HER2-negative advanced breast cancer. Nat Commun. 2022 Jul 15;13(1):4116. doi: 10.1038/s41467-022-31668-8.

Study record dates

Study Major Dates

• Study Start (Actual): September 20, 2017
• Primary Completion (Estimated): December 29, 2027
• Study Completion (Estimated): December 29, 2027

Study Registration Dates

• First Submitted: September 13, 2017
• First Submitted That Met QC Criteria: September 13, 2017
• First Posted (Actual): September 15, 2017

Study Record Updates

• Last Update Posted (Actual): February 12, 2024
• Last Update Submitted That Met QC Criteria: February 8, 2024
• Last Verified: February 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Skin Diseases; Neoplasms; Neoplasms by Site; Breast Diseases; Breast Neoplasms; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Antineoplastic Agents; Immunosuppressive Agents; Immunologic Factors; Protein Kinase Inhibitors; MTOR Inhibitors; Palbociclib; Everolimus
• Other Study ID Numbers: TED14856; 2017-000690-36 (EudraCT Number); U1111-1189-4896 (Registry Identifier: ICTRP)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, blank case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Further details on Sanofi's data sharing criteria, eligible studies, and process for requesting access can be found at: https://vivli.org

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No