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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)

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ClinicalTrials.gov Identifier: NCT03284957
Recruitment Status : Recruiting
First Posted : September 15, 2017
Last Update Posted : July 22, 2021
Sponsor:
Information provided by (Responsible Party):
Sanofi

Brief Summary:

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

Condition or disease Intervention/treatment Phase
Breast Cancer Drug: Amcenestrant Drug: Palbociclib Drug: Alpelisib Drug: Everolimus Drug: Abemaciclib Phase 1 Phase 2

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 42 months.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 251 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: 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
Actual Study Start Date : September 20, 2017
Estimated Primary Completion Date : January 2024
Estimated Study Completion Date : January 2024

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer
Drug Information available for: Palbociclib

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 Name: 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 Name: SAR439859

Drug: Palbociclib

Pharmaceutical form: capsule

Route of administration: oral

Other Name: 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 Name: SAR439859

Drug: Alpelisib

Pharmaceutical form: tablet

Route of administration: oral


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 Name: 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 Name: SAR439859

Drug: Abemaciclib
Pharmaceutical form: tablet




Primary Outcome Measures :
  1. Dose Limiting Toxicities (DLTs) [ Time Frame: Cycle 1, Day 28 for each treated participant (each cycle is 28 days) ]
    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)

  2. Objective Response Rate (ORR) [ Time Frame: Baseline to date of first documentation of progression, assessed up to approximately 6 months after the last entered participant ]
    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)

  3. Adverse Events [ Time Frame: Up to 30 days after last dose of amcenestrant ]
    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)


Secondary Outcome Measures :
  1. Adverse Events [ Time Frame: Up to 30 days after last dose of amcenestrant ]
    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

  2. ORR [ Time Frame: Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant ]
    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

  3. Time to First Response (TTR) [ Time Frame: Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant ]
    Time from the start of treatment to the first objective tumor response observed for participants who achieved CR or PR in all treatment arms

  4. Clinical Benefit Rate (CBR) [ Time Frame: Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant ]
    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

  5. Duration of response [ Time Frame: Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant ]
    Time from initial response to the first documented tumor progression in all treatment arms

  6. tlag of amcenestrant after single dose [ Time Frame: Cycle 1, Day 1 and Day 3 (each cycle is 28 days) ]
    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)

  7. tmax of amcenestrant after single dose [ Time Frame: Cycle 1, Day 1 and Day 3 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arms #1, #2, #4, and #5)

  8. Cmax of amcenestrant after single dose [ Time Frame: Cycle 1, Day 1 and Day 3 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arms #1, #2, #4, and #5)

  9. AUC0-24 of amcenestrant after single dose [ Time Frame: Cycle 1, Day 1 and Day 3 (each cycle is 28 days) ]
    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)

  10. tmax of amcenestrant after repeated dose administration [ Time Frame: Cycle 1, Day 21 or 22 (each cycle is 28 days) ]
    tmax is time to reach Cmax in all treatment arms

  11. Cmax of amcenestrant after repeated dose administration [ Time Frame: Cycle 1, Day 21 or 22 (each cycle is 28 days) ]
    Cmax is maximum concentration observed in all treatment arms

  12. AUC0-24 of amcenestrant after repeated dose administration [ Time Frame: Cycle 1, Day 21 or 22 (each cycle is 28 days) ]
    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

  13. Ctrough of amcenestrant during repeated dose administration [ Time Frame: Cycle 1, Day 8, Day 21 or 22 and Cycle 2, Day 1 (each cycle is 28 days) ]
    Ctrough is plasma concentration observed just before treatment administration during repeated dosing in all treatment arms

  14. tmax of palbociclib after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arm #2)

  15. Cmax of palbociclib after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arm #2)

  16. AUC0-24 of palbociclib after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #2)

  17. tmax of palbociclib after repeated dose administration [ Time Frame: Cycle 1, Day 21 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arm #2)

  18. Cmax of palbociclib after repeated dose administration [ Time Frame: Cycle 1, Day 21 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arm #2)

  19. AUC0-24 of palbociclib after repeated dose administration [ Time Frame: Cycle 1, Day 21 (each cycle is 28 days) ]
    AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #2)

  20. Urine excretion of amcenestrant [ Time Frame: Cycle 1, Day 21 (each cycle is 28 days) ]
    Urine excretion of amcenestrant during the monotherapy expansion phase (Arm #1 Part B)

  21. Cholesterol concentration ratios [ Time Frame: Up to Cycle 2 (each cycle is 28 days) ]
    Plasma 4B hydroxy/total cholesterol concentration ratios (Arm #1)

  22. ER occupancy at 18F-FES-PET imaging [ Time Frame: Baseline and one assessment in Cycle 1 on Day 11 to 15 (each cycle is 28 days) ]
    Inhibition of ER occupancy at 18F-FES-PET imaging (signal extinction) (Arm #1 Part A)

  23. Progression free survival [ Time Frame: Baseline to the date of first documentation of progression, assessed approximately up to 6 months after the last entered participant ]
    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 Arm #1 Part B) per RECIST 1.1, or death (due to any cause), whichever comes first.

  24. Observation of tumor changes by FES PET and FDG PET scans [ Time Frame: Baseline and approximately at Day 15 of Cycle 1 in Part A (each cycle is 28 days) ]
    To correlate the changes observed in FES PET scan with the changes in glucose metabolism seen on FDG PET (Arm #1 Part A)

  25. tmax of alpelisib after third dose [ Time Frame: Cycle 1, Day 3 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arm #3)

  26. Cmax of alpelisib after third dose [ Time Frame: Cycle 1, Day 3 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arm #3)

  27. AUC0-24 of alpelisib after third dose [ Time Frame: Cycle 1, Day 3 (each cycle is 28 days) ]
    AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #3)

  28. tmax of alpelisib after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arm #3)

  29. Cmax of alpelisib after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arm #3)

  30. AUC0-24 of alpelisib after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #3)

  31. tmax of everolimus after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arm #4)

  32. Cmax of everolimus after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arm #4)

  33. AUC0-24 of everolimus after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #4)

  34. tmax of everolimus after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arm #4)

  35. Cmax of everolimus after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arm #4)

  36. AUC0-24 of everolimus after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #4)

  37. tmax of abemaciclib after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arm #5)

  38. Cmax of abemaciclib after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arm #5)

  39. AUC0-24 of abemaciclib after single dose [ Time Frame: Cycle 1, Day 1 (each cycle is 28 days) ]
    AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #5)

  40. tmax of abemaciclib after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    tmax is time to reach Cmax (Arm #5)

  41. Cmax of abemaciclib after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    Cmax is maximum concentration observed (Arm #5)

  42. AUC0-24 of abemaciclib after repeated dose administration [ Time Frame: Cycle 1, Day 22 (each cycle is 28 days) ]
    AUC0-24 is area under the plasma concentration versus time curve calculated using the trapezoidal method over the dosing interval (24 hours) (Arm #5)



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

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 previously treated with endocrine therapy for advanced disease: at least 6 months exposure to endocrine therapy (Participants with early relapse while on adjuvant endocrine therapy that was initiated ≥24 months ago, or who relapsed < 12 months after completion of adjuvant endocrine therapy are eligible); in Arm #2 Part D, no more than 2 prior lines of endocrine therapy are allowed; in Arm #3 Parts F and G, participants must have received and progressed on Aromatase Inhibitor (AI) in combination with CDK4/6 Inhibitor as the first line (1L) treatment for advanced disease prior to receiving the study treatment, and not followed by additional endocrine therapy for advanced disease before entering the study; for Arm #4 (Parts H and I) and Arm #5 (J and K): no more than 1 prior line of a single endocrine therapy for advanced disease is allowed or for Arm #4 Parts H and I: participants must have received and progressed on a non-steroidal Aromatase Inhibitor (AI) in combination with a CDK4/6 Inhibitor as the first line (1L) treatment for advanced disease prior to receiving the study treatment; For Arms #2, #3,#4, and #5 (Parts C, D, F, G, H, I, J and K) participants who relapsed while on adjuvant endocrine therapy that was initiated ≥24 months ago, or relapsed < 12 months after completion of adjuvant endocrine therapy are eligible.
  • 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), except fulvestrant with a washout of at least 6 weeks prior to the first study drug administration. In Arms #3, #4, and #5 (Parts F, G, H, I, J 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 and moderate cytochrome P450 (CYP) 3A or CYP2C8 inducers within 2 weeks before first study treatment
  • 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 (Parts A and B), Arm #2 (Part C), and Arm #3 (Parts F and G)
  • 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) 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.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03284957


Contacts
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Contact: Trial Transparency email recommended (Toll free number for US & Canada) 800-633-1610 ext 1 then # Contact-Us@sanofi.com

Locations
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Sponsors and Collaborators
Sanofi
Investigators
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Study Director: Clinical Sciences & Operations Sanofi
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Responsible Party: Sanofi
ClinicalTrials.gov Identifier: NCT03284957    
Other Study ID Numbers: TED14856
2017-000690-36 ( EudraCT Number )
U1111-1189-4896 ( Other Identifier: UTN )
First Posted: September 15, 2017    Key Record Dates
Last Update Posted: July 22, 2021
Last Verified: July 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: Individual participant data (IPD) and supporting clinical documents are available for request at clinicalstudydatarequest.com. While making information available Sanofi continues to protect the privacy of the participants in clinical trials and to remove commercially confidential information (CCI). Details on Data Sharing criteria and process for requesting access can be found at this web address: clinicalstudydatarequest.com

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Breast Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases
Everolimus
Palbociclib
Antineoplastic Agents
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs
Protein Kinase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action