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Breast CancerPhase 2NCT01225172

Study of BMS-754807 Combined With Letrozole or BMS-754807 Alone in Patients With Hormone Receptor-Positive Breast Cancer and Resistance to Non-Steroidal Aromatase Inhibitors

A Phase 2 study testing BMS-754807 and letrozole in people with Breast Cancer, run by Bristol-Myers Squibb at 21 sites in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

The purpose of this study is to evaluate oral doses of BMS-754807 in combination with letrozole or BMS-754807 alone are safe and efficacious in locally advanced or metastatic hormone receptor positive breast cancer subjects who have progressed with prior non-steroidal aromatase inhibitor treatment. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Breast Cancer
What is being tested?
BMS-754807 and letrozole
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
77 participants
Where
21 sitesUnited States
Study dates
31 Dec 2010to 30 Nov 2014
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Postmenopausal women with hormone receptor-positive and HER-2 negative breast cancer
  • Disease progression following non-steroidal aromatase inhibitor treatment

Who cannot join

  • Known symptomatic brain metastasis
  • Medical condition requiring chronic steroids
  • History of Type 1 or 2 Diabetes
  • Uncontrolled or significant cardiovascular (CV) disease
  • Concomitant second malignancies

Trial locations and contacts

21 sites in 1 country.

21 sites in 1 country

United States21 sites
  • Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

    Baltimore, Maryland, 21231-1000

  • Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins

    Baltimore, Maryland, 21231

  • Univ Of Al At Birmingham

    Birmingham, Alabama, 35294

  • Unv. Of Nc At Chapel Hill

    Chapel Hill, North Carolina, 27599-7305

  • Unv. Of Nc At Chapel Hill

    Chapel Hill, North Carolina, 27599

  • Presbyterian Hospital Cancer Research

    Charlotte, North Carolina, 28204

  • University Of Virginia Health System

    Charlottesville, Virginia, 22908

  • University Of Chicago Medical Center

    Chicago, Illinois, 60637

  • Duke University Medical Center-Dept Of Medicine

    Durham, North Carolina, 27710

  • Indiana University Health Goshen Center For Cancer Care

    Goshen, Indiana, 46526

  • Ut Md Anderson Can Ctr.

    Houston, Texas, 77030-4009

  • Ut Md Anderson Can Ctr.

    Houston, Texas, 77030

  • Mayo Clinic

    Jacksonville, Florida, 32224

  • University Of Wisconsin

    Madison, Wisconsin, 53792-6164

  • University Of Wisconsin

    Madison, Wisconsin, 53792

  • Masonic Cancer Ctr, University Of Minnesota

    Minneapolis, Minnesota, 55455

  • Illinois Cancercare, Pc

    Peoria, Illinois, 61615

  • Mayo Clinic

    Rochester, Minnesota, 55905

  • Sharp Clinical Oncology Research

    San Diego, California, 92123

  • Mayo Clinic Arizona

    Scottsdale, Arizona, 85259

  • Oncology Care Associates, P.A.

    Wheaton, Maryland, 20902

Other trials in United States

About this study

Official title: A Phase 2 Study of BMS-754807 Combined With Letrozole or BMS-754807 Alone in Hormone Receptor-Positive Breast Cancer Subjects With Acquired Resistance to Non-Steroidal Aromatase Inhibitors

The purpose of this study is to evaluate oral doses of BMS-754807 in combination with letrozole or BMS-754807 alone are safe and efficacious in locally advanced or metastatic hormone receptor positive breast cancer subjects who have progressed with prior non-steroidal aromatase inhibitor treatment.

Conditions
Breast Cancer
Being tested
BMS-754807, letrozole
Medical subject headings
Breast Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BMS-754807Drug

    Tablet, Oral, 100 mg, Daily, Until disease progression or unacceptable toxicity

  • letrozoleDrug

    Also called Femara®

    Tablets, Oral, 2.5 mg, Daily, Until disease progression or unacceptable toxicity

Study groups in NCT01225172
Study groupRoleWhat they receive
BMS-754807ExperimentalNot described
Receives: Drug: BMS-754807
BMS-754807 + letrozoleExperimentalNot described
Receives: Drug: BMS-754807; Drug: letrozole

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Progression Free Survival Rate at 24 Weeks

    Progression free survival (PFS) rate at 24 weeks after treatment with BMS 754807/letrozole was to be calculated as the total number of subjects neither progressed nor died after 24 weeks of treatment divided by the total number of subjects (with measurable or non-measurable disease) randomized/assigned to combination treatment arm and treated. In participants with measurable disease Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) criteria was to be used to assess disease progression.This outcome was not measured due to early termination of the study.

    Measured: 24 weeks after initiation of study treatment

Secondary outcomes (7)
  1. The Objective Response Rate (ORR) in Participants With Measurable Disease

    ORR is defined as the number of participants with best overall response (OR) of confirmed complete response (CR) or partial response (PR) divided by the number of participants who received treatment.

    Participants were to be evaluated for tumor response per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions.: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR. This outcome measure was not met due to early termination of the study

    Measured: 24 weeks after initiation of study treatment

  2. Number of Participants With Adverse Events (AEs), Serious AEs, Non-serious AEs , Discontinuation Due to AEs and Deaths

    An Adverse Event (AE) is defined as any new untoward medical occurrence or worsening of a pre-existing medical condition in a patient or clinical investigation subject administered an investigational (medicinal) product and that does not necessarily have a causal relationship with this treatment.

    Measured: Non-SAEs: Day 1 to 7 days after the participant discontinues study medication or 7 days after the End of Treatment visit (up to 42 months), For SAEs: during the screening period and within 30 days of discontinuation of dosing ,up to 42 months

  3. Duration of Response (DOR) in Participants With Measurable Disease

    DOR was to be performed to further characterize the response rate at Week 24. Duration of response is defined as the time between the Week 25 date of response and the date of objectively documented disease progression as defined by modified RECIST 1.1 criteria or death, whichever occurs first. DOR could not be assessed due to early termination of the study.

    Measured: 24 weeks after initiation of study treatment

  4. Number of On-study Laboratory Abnormalities: Grade 1-2

    Blood and urine samples were obtained at specified times points for laboratory evaluations. Clinical Laboratory Sage Panels included: Hematology: Hemoglobin, Hematocrit, Red blood cell, Total leukocyte count, including differential, Platelet count. Serum Chemistry : Albumin, Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), Alkaline phosphatase (ALK-P), Bilirubin, total (TB). Reflex testing of direct (conjugated) and indirect (unconjugated) bilirubin will be ordered if total bilirubin > 5X ULN, Blood urea nitrogen (BUN or urea), Calcium, Chloride, Cholesterol, Creatinine, serum, Glucose, fasting plasma, Lactate dehydrogenase (LDH), Magnesium, Phosphorus, Potassium, Protein, total, Sodium, Triglycerides, Uric acid Urinalysis, Blood, Glucose, Ketones, Leukocyte esterase, pH, Protein. Laboratory tests were graded using the National Cancer Institute-Common Toxicity Criteria for Adverse Events (CTCAE), Version 4.0 criteria

    Measured: Assessed from day 1 up to within 30 days of last dose (Approximately 42 months)

  5. Number of On-study Laboratory Abnormalities: Grade 3-4

    Blood and urine samples were obtained at specified times points for laboratory evaluations. Clinical Laboratory Sage Panels included: Hematology: Hemoglobin, Hematocrit, Red blood cell, Total leukocyte count, including differential, Platelet count. Serum Chemistry : Albumin, Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), Alkaline phosphatase (ALK-P), Bilirubin, total (TB). Reflex testing of direct (conjugated) and indirect (unconjugated) bilirubin will be ordered if total bilirubin > 5X ULN, Blood urea nitrogen (BUN or urea), Calcium, Chloride, Cholesterol, Creatinine, serum, Glucose, fasting plasma, Lactate dehydrogenase (LDH), Magnesium, Phosphorus, Potassium, Protein, total, Sodium, Triglycerides, Uric acid Urinalysis, Blood, Glucose, Ketones, Leukocyte esterase, pH, Protein Laboratory tests were graded using the National Cancer Institute-Common Toxicity Criteria for Adverse Events (CTCAE), Version 4.0 criteria

    Measured: Assessed from day 1 up to within 30 days of last dose (Approximately 42 months)

  6. Treatment Failure Rate (TFR)

    The TFR was to be calculated as the total number of subjects who discontinued the treatment for any reason (including disease progression, treatment toxicity, and death) at 24 weeks divided by the total number of subjects randomized/assigned to the arm and treated. In the monotherapy arm, the TFR was to be assessed while subjects were on monotherapy.

    Measured: 24 weeks after initiation of study treatment

  7. Changes in Absolute Copy Numbers and Relative Expression of Insulin Receptor Isoform A (IR-A) in Tumor Tissue in Response to Treatment

    Absolute copy numbers and relative expression of insulin receptor isoforms (IR-A, IR-B) in pre- and posttreatment fresh tumor tissues were to be measured. This outcome was not measured due to early termination of the study.

    Measured: 24 weeks after initiation of study

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Oct 2010 (estimated)
  2. Study start31 Dec 2010
  3. Primary completion30 Nov 2014
  4. Study completion30 Nov 2014

Why it stopped: Business objectives have changed.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
77 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01225172
Sponsor's protocol ID
CA191-011
Status last verified
Aug 2020
First submitted
19 Oct 2010
Last updated
11 Aug 2020
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing BMS-754807 and letrozole in people with Breast Cancer, run by Bristol-Myers Squibb at 21 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 11 Aug 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 21 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 11 Jul 2019). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Progression Free Survival Rate at 24 Weeks (time frame: 24 weeks after initiation of study treatment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Aug 2020.

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