Breast NeoplasmsPhase 2NCT02258451
Study of Radium-223 Dichloride in Combination With Exemestane and Everolimus Versus Placebo in Combination With Exemestane and Everolimus in Subjects With Bone Predominant HER2 Negative Hormone Receptor Positive Metastatic Breast Cancer
A Phase 2 study testing Radium-223 dichloride (Xofigo, BAY88-8223), Exemestane and Everolimus in people with Breast Neoplasms, run by Bayer at 92 sites in 17 countries.
Trial summary
The objective of this study is to assess efficacy and safety of radium 223 dichloride in subjects with human epidermal growth factor receptor 2 (HER2) negative hormone receptor positive breast cancer with bone metastases treated with exemestane and everolimus After implementation of CSP Amendment 10, only a limited… Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Breast Neoplasms
- What is being tested?
- Radium-223 dichloride (Xofigo, BAY88-8223), Exemestane and Everolimus
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 283 participants
- Where
- 92 sitesin 17 countries
- Study dates
- 4 Jun 2015to 28 Oct 2022
- 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
- Women (≥18 years of age) with metastatic breast cancer not amenable to curative treatment by surgery or radiotherapy.
- Documentation of histological or cytological confirmation of estrogen receptor positive (ER+) and HER2 negative adenocarcinoma of the breast must be available.
- Documentation of menopausal status: postmenopausal subjects or pre-menopausal subjects with ovarian radiation or concomitant therapy with a luteinizing hormone-releasing hormone (LH-RH) agonist/antagonist are eligible.
- Subjects with bone dominant disease with at least 2 skeletal metastases identified at baseline by bone scintigraphy and confirmed by computed tomography (CT)/magnetic resonance imaging (MRI).
- Subjects must have received at least one line of hormonal therapy in the metastatic setting.
- Subjects who are eligible as per the Investigator's assessment and according to the local label for treatment with exemestane and everolimus as a second line or greater of hormone therapy in a metastatic setting.
Show all 10Show fewer
- Subjects must have experienced recurrent/progressive disease following treatment with a non-steroidal aromatase inhibitor (letrozole or anastrozole) in an adjuvant or metastatic setting
- Subjects must have experienced no more than two skeletal-related events (SREs) prior to study entry defined as: need for external beam radiotherapy (EBRT) to bone pain, pathological bone fracture (excluding major trauma), spinal cord compression and/or orthopedic surgical procedure. Subjects with no prior SREs are not permitted.
- Subjects must be on therapy with bisphosphonates or denosumab for at least 1 month before start of study treatment.
- Adequate hematological, liver and kidney function.
Who cannot join
- Subjects with Inflammatory breast cancer.
- Patients with immediately life-threatening visceral disease for whom chemotherapy is preferred treatment option.
- Subjects who have either received chemotherapy for metastatic disease or are considered by the treating investigator to be appropriate candidates for chemotherapy as current treatment for metastatic breast cancer are excluded. Chemotherapy administered for adjuvant/neo adjuvant disease is acceptable provided it was administered at least 1 year prior to study entry.
- Subjects who received prior treatment or are already receiving everolimus treatment prior to study entry are not eligible.
- Subjects with known or history of brain metastases or leptomeningeal disease: subjects with neurological symptoms must undergo a contrast CT scan or MRI of the brain within 28 days prior to randomization to exclude active brain metastasis. Imaging of the central nervous system (CNS) is otherwise not required.
Trial locations and contacts
92 sites in 17 countries.
92 sites in 17 countries
United States15 sites
Study site
Ann Arbor, Michigan, 48109
Study site
Ashland, Kentucky, 41101
Study site
Detroit, Michigan, 48202
Study site
Hollywood, Florida, 33021
Study site
Jamaica, New York, 11432
Study site
La Jolla, California, 92093
Study site
Los Angeles, California, 90033
Study site
New Haven, Connecticut, 6510
Study site
Newark, New Jersey, 07103
Study site
Pontiac, Michigan, 48341
Study site
Rochester, Minnesota, 55905
Study site
Rockville, Maryland, 20850
Study site
Spokane, Washington, 99208-1129
Study site
St Louis, Missouri, 63110
Study site
Watertown, South Dakota, 57201
Spain11 sites
Study site
Barcelona, 08023
Study site
Barcelona, 08041
Study site
Barcelona, 8036
Study site
Madrid, 28033
Study site
Madrid, 28041
Study site
Madrid, 28046
Study site
Madrid, 28050
Study site
Palma de Mallorca, Illes Baleares, 07120
Study site
Pamplona, 31008
Study site
Seville, 41013
Study site
Seville, 41071
Italy10 sites
Study site
Bari, Apulia, 70124
Study site
Bologna, Emilia-Romagna, 40138
Study site
Cremona, Lombardy, 26100
Study site
Forlì Cesena, Emilia-Romagna, 47014
Study site
Genoa, Liguria, 16128
Study site
Milan, Lombardy, 20132
Study site
Modena, Emilia-Romagna, 41124
Study site
Pisa, Tuscany, 56126
Study site
Rome, Lazio, 00149
Study site
Rome, Lazio, 00161
Israel9 sites
Study site
Afula, 1834111
Study site
Beersheba, 8410101
Study site
Haifa, 3109601
Study site
Holon, 5822012
Study site
Jerusalem, 9103102
Study site
Jerusalem, 9112001
Study site
Ramat Gan, 5262000
Study site
Tel Aviv, 64239
Study site
Zrifin, 7030000
Japan8 sites
Study site
Hidaka, Saitama, 350-1298
Study site
Kagoshima, 892-0833
Study site
Kita-Adachigun, Saitama, 362-0806
Study site
Koto-ku, Tokyo, 135-8550
Study site
Nagoya, Aichi-ken, 464-8681
Study site
Osaka, 540-0006
Study site
Sapporo, Hokkaido, 060-8648
Study site
Sayama, Osaka, 589-8511
South Korea6 sites
Study site
Busan, 49241
Study site
Daegu, 42601
Study site
Incheon
Study site
Seoul, Seoul Teugbyeolsi, 03080
Study site
Seoul, 05505
Study site
Suwon, Gyeonggido, 442-723
France5 sites
Study site
Angers, 49055
Study site
Nantes, 44805
Study site
Nîmes, 30029
Study site
Saint-Cloud, 92210
Study site
Tours, 37044
Poland5 sites
Study site
Bialystok, 15-027
Study site
Gdansk, 80-952
Study site
Gdynia, 81-519
Study site
Poznan, 61-485
Study site
Warsaw, 02-781
United Kingdom5 sites
Study site
Bristol, BS2 8ED
Study site
Nottingham, Nottinghamshire, NG5 1PB
Study site
Plymouth, Devon, PL6 8DH
Study site
Taunton, Somerset, TA1 5DA
Study site
Truro, Cornwall, TR1 3LJ
Belgium4 sites
Study site
Brussels, 1070
Study site
Edegem, 2650
Study site
Kortrijk, 8500
Study site
Leuven, 3000
Taiwan4 sites
Study site
Kaohsiung City, 813414
Study site
Taichung, 40705
Study site
Taipei, 114
Study site
Taipei
Singapore3 sites
Study site
Singapore, 119074
Study site
Singapore, 168583
Study site
Singapore, 258499
About this study
Official title: A Phase II Randomized, Double-blind, Placebo-controlled Trial of Radium-223 Dichloride in Combination With Exemestane and Everolimus Versus Placebo in Combination With Exemestane and Everolimus When Administered to Metastatic HER2 Negative Hormone Receptor Positive Breast Cancer Subjects With Bone Metastases
The objective of this study is to assess efficacy and safety of radium 223 dichloride in subjects with human epidermal growth factor receptor 2 (HER2) negative hormone receptor positive breast cancer with bone metastases treated with exemestane and everolimus
After implementation of CSP Amendment 10, only a limited number of subjects will remain in this study, in order to reduce the burden to study subjects, collection of data will be reduced and will focus mainly on acute safety, SSE, and OS. Once subjects are rolled over, the long-term safety will be collected and assessed entirely in the separate extended safety follow-up study.
- Conditions
- Breast Neoplasms
- Being tested
- Radium-223 dichloride (Xofigo, BAY88-8223), Placebo (saline), Exemestane, Everolimus
- Keywords
- Breast Cancer
- Medical subject headings
- Breast Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Radium-223 dichloride (Xofigo, BAY88-8223)Drug
Up to 6 cycles of radium-223 dichloride 50kBq/kg body (55 kBq/kg after implementation of NIST update)
Placebo (saline)Drug
Up to 6 cycles of saline injection
ExemestaneDrug
One 25 mg tablet once daily after a meal.
EverolimusDrug
The recommended dose of everolimus administered in the study is 10 mg once daily with or without food.
Starting dose, dose modifications, and administration of exemestane and everolimus must be in compliance with the local labels in each of the participating countries and/or in line with local standard of practice.
| Study group | Role | What they receive |
|---|---|---|
| Radium-223 dichloride + exemestane/everolimus | Experimental | Up to 6 cycles of radium-223 dichloride 50kBq/kg body weight (55 kBq/kg after implementation of National Institute of Standards and Technology [NIST] update) (randomized). Participants will also receive exemestane, 25-mg tablet once daily (after a meal), and everolimus, 10 mg once daily (with or without food), and supportive care as per the local or institutional standard of practice. Receives: Drug: Radium-223 dichloride (Xofigo, BAY88-8223); Drug: Exemestane; Drug: Everolimus |
| Placebo + exemestane/everolimus | Placebo comparator | Up to 6 cycles of saline injection (placebo) (randomized). Participants will also receive exemestane, 25-mg tablet once daily (after a meal), and everolimus, 10 mg once daily (with or without food), and supportive care as per the local or institutional standard of practice. Receives: Drug: Placebo (saline); Drug: Exemestane; Drug: Everolimus |
What is being measured
The primary outcome is the main question the study is designed to answer.
Symptomatic Skeletal Event-free Survival (SSE-FS)
Time from date of randomization to occurrence of one of the following, whichever happened earlier: 1) an on study SSE, which was defined as the use of external beam radiotherapy (EBRT) to relieve skeletal symptoms, the occurrence of new symptomatic pathological bone fractures (vertebral or nonvertebral), the occurrence of spinal cord compression, a tumor related orthopedic surgical intervention; or 2) death from any cause. Per Protocol Amendment 10, following primary analysis completion, further assessments were focused on safety, and only limited efficacy data including SSE and survival were collected and not designed to support reconsideration of the primary analysis efficacy conclusions. Accordingly, no formal statistical analyses were performed for primary and secondary efficacy outcomes in the final analysis. All primary and secondary efficacy outcome measures presented in this document came from the primary completion analysis.
Measured: Up to 55 months
Secondary outcomes (10)
Overall Survival
The time from the date of randomization to the date of death due to any cause. Per Protocol Amendment 10, following primary analysis completion, further assessments were focused on safety, and only limited efficacy data including SSE and survival were collected and not designed to support reconsideration of the primary analysis efficacy conclusions. Accordingly, no formal statistical analyses were performed for primary and secondary efficacy outcomes in the final analysis. All primary and secondary efficacy outcome measures presented in this document came from the primary completion analysis.
Measured: Up to 55 months
Time to Opiate Use for Cancer Pain
Interval from the date of randomization to the date of opiate use
Measured: Up to 55 months
Time to Pain Progression
Time from randomization to the first date a participant experienced pain progression based on WPS. Pain progression was defined as an increase of 2 or more points in the BPI-SF "Worst pain in 24 hours" score from baseline observed at 2 consecutive evaluations ≥4 weeks apart or an increase in pain management (IPM) with respect to baseline, whichever occurred first. An IPM is defined as the initiation of any opioid in participants not taking opioids at baseline, the initiation of a strong opioid in participants taking a weak opioid at baseline, or the initiation of an additional strong opioid in participants taking a strong opioid at baseline.
Measured: Up to 55 months
Time to Cytotoxic Chemotherapy
Time from the date of randomization to the date of the first cytotoxic chemotherapy
Measured: Up to 55 months
Radiological Progression-free Survival (rPFS)
Time from the date of randomization to the date of confirmed radiological progression in either soft tissue, viscera or bone, or death (if death occurs before progression). Progression is defined using the modified RECIST 1.1 criteria (the modification refers to bone lesions assessment). Progression is defined as a 20% increase in the sum of the longest diameter of target lesions, or an unequivocal increase in non-target lesions, or the appearance of new lesions. All bone lesions are considered non-measurable and new bone lesions identified by bone scan should be confirmed by further imaging (CT/MRI). If a new bone lesion or unequivocal increase in size of bone lesions is only visible on a CT/MRI and not visible on a technetium-99m bone scan, progression should be declared without further confirmation.
Measured: Up to 55 months
Percentage of Participants With Pain Improvement
In the percentage of participants with confirmed pain improvement. Confirmed pain improvement is defined a 2-point decrease or more in BPI-SF WPS from baseline over 2 consecutive measurements conducted at least 4 weeks apart, without an increase in pain management (IPM). An IPM is defined as the initiation of any opioid in participants not taking opioids at baseline, the initiation of a strong opioid in participants taking a weak opioid at baseline, or the initiation of an additional strong opioid in participants taking a strong opioid at baseline.
Measured: Up to 55 months
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
An AE was any untoward medical occurrence (i.e. any unfavorable and unintended sign [including abnormal laboratory findings], symptom or disease) in a patient or clinical investigation participant after providing written informed consent for participation in the study. AEs were considered to be treatment-emergent if they started or worsened after first application of study intervention up to 30 days after end of treatment with study intervention. A serious adverse event (SAE) was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening; persistent or significant disability/incapacity; congenital anomaly; another medical important serious event as judged by the investigator and an occurrence of any additional malignancies, including acute myelocytic leukemia or hematological conditions.
Measured: From first dosing up to 30 days after the last administration of study treatments, up to 72.6 months
Number of Participants With Post-treatment Chemotherapy Related Adverse Events
According to protocol amendment 10, all participants who completed the EOT visit will be transferred to a separate extended safety follow-up study for their remaining follow-up. Thus, no further post-treatment data were collected after protocol amendment 10.
Measured: From post-treatment till end of study, up to 45.8 months
Number of Participants With Hematological Toxicities: Worst Grade Under Treatment
Measured: From first dosing up to 30 days after the last administration of study treatments, up to 72.6 months
Number of Participants With New Primary Malignancies
Measured: From first dosing till end of study, up to 72.6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Oct 2014 (estimated)
- Study start4 Jun 2015
- Primary completion22 Jan 2020
- Study completion28 Oct 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Breast NeoplasmsStudies of the same condition, open and under way.
- More trials run by BayerThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 283 participants (actual)
Sponsor and investigators
- Lead sponsor
- Bayer
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Bayer Study Director, Study director, Bayer
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02258451
- Sponsor's protocol ID
- 17096
- Other IDs
- 2014-002114-23, 2014
- Status last verified
- Nov 2023
- First submitted
- 30 Sep 2014
- Last updated
- 24 Nov 2023
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
Publications
Rugo HS, Van Poznak CH, Neven P, Danielewicz I, Lee SC, Campone M, Chik JYK, Vega Alonso E, Naume B, Brain E, Siegel JM, Li R, Uema D, Wagner VJ, Coleman RE. Radium-223 in women with hormone receptor-positive bone-metastatic breast cancer receiving endocrine therapy: pooled analysis of two international, phase 2, randomized, double-blind, placebo-controlled trials. Breast Cancer Res Treat. 2024 Apr;204(2):249-259. doi: 10.1007/s10549-023-07147-z. Epub 2023 Dec 20.
PubMed 38123789
Study at a glance
From the registry record, last updated by the sponsor on 24 Nov 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase II Randomized, Double-blind, Placebo-controlled Trial of Radium-223 Dichloride in Combination With Exemestane and Everolimus Versus Placebo in Combination With Exemestane and Everolimus When Administered to Metastatic HER2 Negative Hormone Receptor Positive Breast Cancer Subjects With Bone Metastases
- ClinicalTrials.gov ID
- NCT02258451
- Acronym / sponsor ID
- 17096
- Conditions
- Breast Neoplasms
- Keywords
- Breast Cancer
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 283 participants (actual)
- Lead sponsor
- BayerIndustry (pharma, biotech, devices)
- Study start
- 4 Jun 2015 (actual)
- Primary completion
- 22 Jan 2020 (actual)
- Study completion
- 28 Oct 2022 (actual)
- First posted
- 7 Oct 2014 (estimated)
- Results
- Posted 10 Mar 2022
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The objective of this study is to assess efficacy and safety of radium 223 dichloride in subjects with human epidermal growth factor receptor 2 (HER2) negative hormone receptor positive breast cancer with bone metastases treated with exemestane and everolimus
After implementation of CSP Amendment 10, only a limited number of subjects will remain in this study, in order to reduce the burden to study subjects, collection of data will be reduced and will focus mainly on acute safety, SSE, and OS. Once subjects are rolled over, the long-term safety will be collected and assessed entirely in the separate extended safety follow-up study.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Radium-223 dichloride + exemestane/everolimus | Experimental | Drug: Radium-223 dichloride (Xofigo, BAY88-8223), Drug: Exemestane, Drug: EverolimusUp to 6 cycles of radium-223 dichloride 50kBq/kg body weight (55 kBq/kg after implementation of National Institute of Standards and Technology [NIST] update) (randomized). Participants will also receive exemestane, 25-mg tablet once daily (after a meal), and everolimus, 10 mg once daily (with or without food), and supportive care as per the local or institutional standard of practice. |
| Placebo + exemestane/everolimus | Placebo comparator | Drug: Placebo (saline), Drug: Exemestane, Drug: EverolimusUp to 6 cycles of saline injection (placebo) (randomized). Participants will also receive exemestane, 25-mg tablet once daily (after a meal), and everolimus, 10 mg once daily (with or without food), and supportive care as per the local or institutional standard of practice. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- Women (≥18 years of age) with metastatic breast cancer not amenable to curative treatment by surgery or radiotherapy.
- Documentation of histological or cytological confirmation of estrogen receptor positive (ER+) and HER2 negative adenocarcinoma of the breast must be available.
- Documentation of menopausal status: postmenopausal subjects or pre-menopausal subjects with ovarian radiation or concomitant therapy with a luteinizing hormone-releasing hormone (LH-RH) agonist/antagonist are eligible.
- Subjects with bone dominant disease with at least 2 skeletal metastases identified at baseline by bone scintigraphy and confirmed by computed tomography (CT)/magnetic resonance imaging (MRI).
- Subjects must have received at least one line of hormonal therapy in the metastatic setting.
Key exclusion criteria (5 listed)
- Subjects with Inflammatory breast cancer.
- Patients with immediately life-threatening visceral disease for whom chemotherapy is preferred treatment option.
- Subjects who have either received chemotherapy for metastatic disease or are considered by the treating investigator to be appropriate candidates for chemotherapy as current treatment for metastatic breast cancer are excluded. Chemotherapy administered for adjuvant/neo adjuvant disease is acceptable provided it was administered at least 1 year prior to study entry.
- Subjects who received prior treatment or are already receiving everolimus treatment prior to study entry are not eligible.
- Subjects with known or history of brain metastases or leptomeningeal disease: subjects with neurological symptoms must undergo a contrast CT scan or MRI of the brain within 28 days prior to randomization to exclude active brain metastasis. Imaging of the central nervous system (CNS) is otherwise not required.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Radium-223 dichloride (Xofigo, BAY88-8223)Up to 6 cycles of radium-223 dichloride 50kBq/kg body (55 kBq/kg after implementation of NIST update) | Drug | Radium-223 dichloride + exemestane/everolimus |
| Placebo (saline)Up to 6 cycles of saline injection | Drug | Placebo + exemestane/everolimus |
| ExemestaneOne 25 mg tablet once daily after a meal. | Drug | Placebo + exemestane/everolimus, Radium-223 dichloride + exemestane/everolimus |
| EverolimusThe recommended dose of everolimus administered in the study is 10 mg once daily with or without food. Starting dose, dose modifications, and administration of exemestane and everolimus must be in compliance with the local labels in each of the participating countries and/or in line with local standard of practice. | Drug | Placebo + exemestane/everolimus, Radium-223 dichloride + exemestane/everolimus |
Primary outcome
Symptomatic Skeletal Event-free Survival (SSE-FS)
Time frame: Up to 55 months
Time from date of randomization to occurrence of one of the following, whichever happened earlier: 1) an on study SSE, which was defined as the use of external beam radiotherapy (EBRT) to relieve skeletal symptoms, the occurrence of new symptomatic pathological bone fractures (vertebral or nonvertebral), the occurrence of spinal cord compression, a tumor related orthopedic surgical intervention; or 2) death from any cause. Per Protocol Amendment 10, following primary analysis completion, further assessments were focused on safety, and only limited efficacy data including SSE and survival were collected and not designed to support reconsideration of the primary analysis efficacy conclusions. Accordingly, no formal statistical analyses were performed for primary and secondary efficacy outcomes in the final analysis. All primary and secondary efficacy outcome measures presented in this document came from the primary completion analysis.
10 secondary outcomes
Overall Survival
Time frame: Up to 55 months
Time to Opiate Use for Cancer Pain
Time frame: Up to 55 months
Time to Pain Progression
Time frame: Up to 55 months
Time to Cytotoxic Chemotherapy
Time frame: Up to 55 months
Radiological Progression-free Survival (rPFS)
Time frame: Up to 55 months
Percentage of Participants With Pain Improvement
Time frame: Up to 55 months
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
Time frame: From first dosing up to 30 days after the last administration of study treatments, up to 72.6 months
Number of Participants With Post-treatment Chemotherapy Related Adverse Events
Time frame: From post-treatment till end of study, up to 45.8 months
Number of Participants With Hematological Toxicities: Worst Grade Under Treatment
Time frame: From first dosing up to 30 days after the last administration of study treatments, up to 72.6 months
Number of Participants With New Primary Malignancies
Time frame: From first dosing till end of study, up to 72.6 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Nov 2023.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 38123789Rugo HS, Van Poznak CH, Neven P, Danielewicz I, Lee SC, Campone M, Chik JYK, Vega Alonso E, Naume B, Brain E, Siegel JM, Li R, Uema D, Wagner VJ, Coleman RE. Radium-223 in women with hormone receptor-positive bone-metastatic breast cancer receiving endocrine therapy: pooled analysis of two international, phase 2, randomized, double-blind, placebo-controlled trials. Breast Cancer Res Treat. 2024 Apr;204(2):249-259. doi: 10.1007/s10549-023-07147-z. Epub 2023 Dec 20.
- Click here to find information about studies related to Bayer Healthcare products conducted in EuropeLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Bayer Study Director study director
Bayer
92 sites in 17 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Radium-223 dichloride (Xofigo, BAY88-8223), Exemestane and Everolimus in people with Breast Neoplasms, run by Bayer at 92 sites in 17 countries.
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 10 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: finished, as of the sponsor's last update on 24 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 92 sites in United States, Spain, Italy, Israel, Japan and 12 more countries. 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. Some participants in this study may receive a placebo. 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 10 Mar 2022). 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?
Symptomatic Skeletal Event-free Survival (SSE-FS) (time frame: Up to 55 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02258451, which also lists 1 linked publication.
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 24 Nov 2023.