ABEMACICLIB for Breast cancer

Inclusion criteria

• {"criterion_text":"- Have a diagnosis of HR+, HER2- breast cancer\n- Have locally advanced disease not amenable to curative treatment by surgery or metastatic disease. In addition, participants must fulfill 1 of the following criteria: - relapsed with radiologic evidence of progression while receiving neoadjuvant or adjuvant endocrine therapy, with no subsequent endocrine therapy received following progression - relapsed with radiologic evidence of progression within 1 year from completion of adjuvant endocrine therapy, with no subsequent endocrine therapy received following progression - relapsed with radiologic evidence of progression more than 1 year from completion of adjuvant endocrine therapy and then subsequently relapsed with radiologic evidence of progression after receiving treatment with either an antiestrogen or an aromatase inhibitor as firstline endocrine therapy for metastatic disease. Patients may not have received more than 1 line of endocrine therapy or any prior chemotherapy for metastatic disease - presented de novo with metastatic disease and then relapsed with Radiologic evidence of progression after receiving treatment with either an antiestrogen or an aromatase inhibitor as first-line endocrine therapy for metastatic disease. Patients may not have received more than 1 line of endocrine therapy or any prior chemotherapy for metastatic disease\n- Have postmenopausal status due to either surgical/natural menopause or ovarian suppression (initiated at least 28 days prior to Day 1 of Cycle 1) with a gonadotropin-releasing hormone (GnRH) agonist such as goserelin\n- Have a negative serum pregnancy test at baseline (within 14 days prior to randomization) and agree to use medically approved precautions to prevent pregnancy during the study and for 12 weeks following the last dose of Abemaciclib if postmenopausal status is due to ovarian suppression with a GnRH agonist\n- Have either measurable disease or nonmeasurable bone only disease\n- Have a performance status ≤1 on the ECOG scale\n- Have discontinued previous therapies for cancer (including specifically, aromatase inhibitors, anti-estrogens, chemotherapy, radiotherapy, and immunotherapy) for at least 21 days for myelosuppressive agents or 14 days for nonmyelosuppressive agents prior to receiving study drug, and recovered from the acute effects of therapy (until the toxicity resolves to either baseline or at least Grade 1) except for residual alopecia or peripheral neuropathy"}

Exclusion criteria

• {"criterion_text":"- Are currently receiving an investigational drug in a clinical trial or participating in any other type of medical research judged not to be scientifically or medically compatible with this study\n- Have visceral crisis, lymphangitic spread, or leptomeningeal carcinomatosis visceral crisis is not the mere presence of visceral metastases but implies severe organ dysfunction as assessed by symptoms and signs, laboratory studies, and rapid progression of the disease\n- Have clinical evidence or history of central nervous system metastasis\n- Have received prior treatment with chemotherapy (except for neoadjuvant/ adjuvant chemotherapy), fulvestrant, everolimus, or any CDK4/6 inhibitor\n- Have received treatment with a drug that has not received regulatory approval for any indication within 14 or 21 days prior to randomization of study drug for a nonmyelosuppressive or myelosuppressive agent, respectively\n- Have received recent (within 28 days prior to randomization) yellow fever vaccination\n- Have had major surgery within 14 days prior to randomization of study drug to allow for post-operative healing of the surgical wound and site(s)\n- Have a personal history within the last 12 months of any of the following conditions: syncope of cardiovascular etiology, ventricular tachycardia, ventricular fibrillation, or sudden cardiac arrest\n- Have inflammatory breast cancer or a history of any other cancer (except nonmelanoma skin cancer or carcinoma in-situ of the cervix), unless in complete remission with no therapy for a minimum of 3 years\n- Have received an autologous or allogeneic stem-cell transplant\n- Have active bacterial or fungal infection, or detectable viral infection\n- Have initiated bisphosphonates or approved RANK ligand (RANK-L) targeted agents (for example, denosumab) <7 days prior to randomization"}

Primary endpoints

• {"endpoint_text":"- Progression-Free Survival (PFS)","definition_or_measurement_approach":""}

Greece

Earliest CTIS Part Ii Submission Date

28-06-2024

Latest Decision Or Authorization Date

30-07-2024

Processing Time Days

32

Number Of Sites

1

Number Of Participants

14

Spain

Earliest CTIS Part Ii Submission Date

29-04-2024

Latest Decision Or Authorization Date

17-05-2024

Processing Time Days

18

Number Of Sites

2

Number Of Participants

3

Belgium

Earliest CTIS Part Ii Submission Date

29-04-2024

Latest Decision Or Authorization Date

22-05-2024

Processing Time Days

23

Number Of Sites

3

Number Of Participants

3

Italy

Earliest CTIS Part Ii Submission Date

29-04-2024

Latest Decision Or Authorization Date

24-05-2024

Processing Time Days

25

Number Of Sites

1

Number Of Participants

2

Poland

Earliest CTIS Part Ii Submission Date

29-04-2024

Latest Decision Or Authorization Date

31-05-2024

Processing Time Days

32

Number Of Sites

1

Number Of Participants

2

Primary sponsor

Full Name

Eli Lilly & Co.

Organisation Type

Pharmaceutical company

Country Of Registered Address

United States

Contract research organisations

Name

Syneos Health Inc.

Responsibilities

Codes: [6]

Name

Pharmaceutical Product Development LLC

Responsibilities

Codes: [10]

Name

Iqvia Rds Inc.

Responsibilities

Codes: [1,5]

Name

Icon Clinical Research Limited

Responsibilities

Codes: [1]

Name

Parexel International Corp.

Responsibilities

Codes: [1,5]

Name

Charles River Laboratories International Inc.

Responsibilities

Codes: [4]

Name

Biotel Research LLC

Responsibilities

Codes: [4]

Name

Q2 Solutions LLC

Responsibilities

Codes: [4]

Third parties

• {"country":"United States","full_name":"Syneos Health Inc.","duties_or_roles":"Codes: [6]","organisation_type":"Pharmaceutical company"}
• {"country":"United States","full_name":"Q2 Solutions LLC","duties_or_roles":"Codes: [4]","organisation_type":"Laboratory/Research/Testing facility"}
• {"country":"United States","full_name":"Biotel Research LLC","duties_or_roles":"Codes: [4]","organisation_type":"Pharmaceutical company"}
• {"country":"United States","full_name":"Pharmaceutical Product Development LLC","duties_or_roles":"Codes: [10]","organisation_type":"Pharmaceutical company"}
• {"country":"United States","full_name":"Iqvia Rds Inc.","duties_or_roles":"Codes: [1,5]","organisation_type":"Pharmaceutical company"}
• {"country":"Ireland","full_name":"Icon Clinical Research Limited","duties_or_roles":"Codes: [1]","organisation_type":"Pharmaceutical company"}
• {"country":"United States","full_name":"Charles River Laboratories International Inc.","duties_or_roles":"Codes: [4]","organisation_type":"Pharmaceutical company"}
• {"country":"United States","full_name":"Parexel International Corp.","duties_or_roles":"Codes: [1,5]","organisation_type":"Pharmaceutical company"}
• {"country":"Singapore","full_name":"Labcorp Development (Asia) Pte Ltd","duties_or_roles":"Codes: [4]","organisation_type":"Pharmaceutical company"}
• {"country":"Greece","full_name":"Pharmaserve Lilly S.A.C.I.","duties_or_roles":"Codes: [1,12,15,2,5]; includes: \"Negotiation and Execution of Clinical trial agreements with the participating sites, make study payments based on invoices\"","organisation_type":"Industry"}
• {"country":"United States","full_name":"Labcorp Central Laboratory Services LP","duties_or_roles":"Codes: [4]","organisation_type":"Pharmaceutical company"}
• {"country":"Switzerland","full_name":"Labcorp Central Laboratory Services SARL","duties_or_roles":"Codes: [4]","organisation_type":"Pharmaceutical company"}