Breast CancerPhase 2NCT00371254
A Study of Dasatinib (BMS-354825) in Patients With Advanced 'Triple-negative' Breast Cancer
A Phase 2 study testing Dasatinib in people with Breast Cancer and Metastasis, run by Bristol-Myers Squibb at 10 sites in 4 countries.
Trial summary
This study will determine whether the investigational drug dasatinib is effective in treatment of women with progressive advanced triple-negative breast cancer. Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Breast Cancer, Metastasis
- What is being tested?
- Dasatinib
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 55 participants
- Where
- 10 sitesin 4 countries
- Study dates
- Dec 2006to Sep 2008
- 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
- females, 18 or older
- recurrent or progressive locally advanced, or 'triple negative' metastatic breast cancer
- paraffin-embedded tissue block must be available
- measurable disease
- prior chemotherapy with an anthracycline, a taxane, or both (neoadjuvant, adjuvant, or metastatic setting)
- 0, 1 or 2 chemotherapies in the metastatic setting
- adequate organ function
Who cannot join
- Metastatic disease confined to bone only
- Symptomatic CNS metastasis
- Concurrent medical condition which may increase the risk of toxicity
- Unable to take oral medication
Trial locations and contacts
10 sites in 4 countries.
10 sites in 4 countries
United States5 sites
Dana-Farber Cancer Inst
Boston, Massachusetts, 02115
University Of Texas Md Anderson Cancer Ctr
Houston, Texas, 77030
Mayo Clinic Jacksonville
Jacksonville, Florida, 32224
Ucsf-Comprehensive Cancer Center
San Francisco, California, 94143
Montefiore Medical Center
The Bronx, New York, 10461
About this study
Official title: Phase II Study of Dasatinib (BMS-354825) for Advanced 'Triple-negative' Breast Cancer
This study will determine whether the investigational drug dasatinib is effective in treatment of women with progressive advanced triple-negative breast cancer.
- Conditions
- Breast Cancer, Metastasis
- Being tested
- Dasatinib
- Keywords
- Recurrent, locally-advanced, or 'triple negative' metastatic breast cancer
- Medical subject headings
- Breast Neoplasms, Neoplasm Metastasis, Recurrence
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
DasatinibDrug
Also called Sprycel, BMS-354825
Tablets, Oral, 100 mg, twice daily as long as the patient benefits (avg <6 months)
DasatinibDrug
Tablets, Oral, 70 mg, twice daily as long as the patient benefits (avg <6 months)
| Study group | Role | What they receive |
|---|---|---|
| 1 | Experimental | Not described Receives: Drug: Dasatinib |
| 2 | Experimental | Not described Receives: Drug: Dasatinib |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Participants With Complete Response (CR) or Partial Response (PR)
Tumor response was defined as the number of participants whose best response was CR or PR, per the Response Evaluation Criteria in Solid Tumor (RECIST): CR: disappearance of all target/non-target lesions; PR: >= 30% decrease in the sum of the LDs of target lesions relative to the baseline sum LD.
Measured: Baseline to end of study drug therapy (up to 65 weeks).
Percentage of Participants With Complete Response (CR) or Partial Response (PR)
The percentage of participants whose best response was CR or PR, per the RECIST: CR: disappearance of all target/non-target lesions; PR: >= 30% decrease in the sum of the LDs of target lesions relative to the baseline sum LD.
Measured: Baseline to end of study drug therapy (up to 65 weeks).
Secondary outcomes (21)
Number of Participants With Complete Response (CR), Partial Response (PR) or Stable Disease (SD) at or After 16 Weeks on Study
The number of participants whose best response was CR, PR or SD (per the RECIST) at or after 16 weeks on study: CR: disappearance of all target/non-target lesions; PR: >=30% decrease in the sum of the LDs of target lesions relative to baseline sum LD; SD: neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD; PD: appearance of new lesion/s, or >=20% increase in the sum of the LD of target lesions, relative to the smallest sum LD recorded since treatment start, or unequivocal progression of existing non-target lesions.
Measured: Baseline to 16 weeks.
Percentage of Participants With Complete Response (CR), Partial Response (PR) or Stable Disease (SD) at or After 16 Weeks on Study
The percentage of participants whose best response was CR, PR or SD (per the RECIST) at or after 16 weeks on study: CR: disappearance of all target/non-target lesions; PR: >=30% decrease in the sum of the LDs of target lesions relative to baseline sum LD; SD: neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD; PD: appearance of new lesion/s, or >=20% increase in the sum of the LD of target lesions, relative to the smallest sum LD recorded since treatment start, or unequivocal progression of existing non-target lesions.
Measured: Baseline to 16 weeks
Proportion of Participants With Progression-Free Survival (PFS) at Weeks 9, 17, and 25
PFS:time from first dose until the date that progressive disease (PD) or clinical PD (cPD) observed,per RECIST criteria.PD:appearance of new lesion/s,or >=20% increase in the sum of the LD of target lesions,relative to smallest sum LD recorded since treatment start,or unequivocal progression of existing non-target lesions;cPD:deterioration related to disease requiring treatment discontinuation,but without radiographic PD.Participants who died without PD were considered to have PD on the date of death.For participants who neither progressed nor died,date of the last tumor assessment was used.
Measured: Weeks 9, 17, and 25
Mean Number of Weeks of Complete Response (CR) or Partial Response (PR)
Mean number of weeks of CR/PR (time from first date of CR/PR until first date PD observed. Tumor response defined per RECIST: CR: disappearance of all target/non-target lesions; PR: >=30% decrease in sum of LDs of target lesions relative to baseline sum LD; PD: appearance of new lesion or >=20% increase in sum of LD of target lesions relative to smallest sum LD or unequivocal progression of existing non-target lesions. Participants who died without reported PD were considered to have PD on date of death. For participants who neither progressed nor died, date of last tumor assessment used.
Measured: Baseline to end of study drug therapy (up to 53.86 weeks)
Mean Plasma Concentration at Week 3
Mean plasma concentration was obtained directly from the concentration-time data.
Measured: At pre-dose and 1, 3, 6 and 12 hours after each dose administration
Mean Plasma Concentration at Week 7
Mean plasma concentration was obtained directly from the concentration-time data.
Measured: At pre-dose and 1, 3, 6 and 12 hours after each dose administration
Mean Change in Concentration of Collagen Type IV From Baseline
Collagen Type IV is a measure of anti-angiogenic activity. Plasma samples for assessment of change in concentration of Collagen Type IV were obtained and analyzed by enzyme-linked immunosorbent assay.
Measured: Baseline, Week 3 and Week 5
Mean Change in Concentration of Vascular Endothelial Growth Factor Receptor-2 (VEGFR2) From Baseline
VEGFR2 is a measure of anti-angiogenic activity. Plasma samples for assessment of change in concentration of VEGFR2 were obtained and analyzed by enzyme-linked immunosorbent assay.
Measured: Baseline, Week 3 and Week 5
Percentage Change in Tumor Biomarkers
Tumor markers are indicators of tumor activity which may be used to predict clinical benefit and circulating biomarkers may reveal key mechanisms of action. Tissue staining was performed for caveolin, phospho-caveolin, EphA2 and insulin-like growth factor binding protein 2 (IGFBP2) markers using immunohistochemistry assays.
Measured: Baseline
Profiling of Messenger-ribonucleic Acid (mRNA) Expression: mRNA Signal Intensity
Pharmacogenomic analysis included the assessment of the relationship between clinical benefit and mRNA expression levels and between clinical benefit and protein phosphorylation. Tumor mRNA expression was analyzed in all available tissues. mRNA was extracted from 96 formalin-fixed paraffin-embedded tissue (FFPET) samples, amplified, and fluorescently labeled. Gene expression profiling was conducted using Affymetrix Human Genome U133A 2.0 DNA microarrays. mRNA expression is reported as quantile normalized RMA values.
Measured: Baseline
Number of Participants Who Died, Experienced Other Serious Adverse Events (SAEs) or Adverse Events (AEs)
An AE was defined as any new untoward medical occurrence or worsening of a pre-existing medical condition (even if not caused by the study drug). An SAE was defined as an AE that resulted in death, was life-threatening, required hospitalization (or prolongation of existing hospitalization), or was an important medical event.
Measured: From start of study drug therapy up to 30 days after the last dose.
Number of Participants Who Experienced Drug-related SAEs, Drug-related AEs, Drug-related Grade 3 AEs and Discontinuations Due to Drug-related AEs
AE=any new untoward medical occurrence/worsening of pre-existing medical condition.SAE=AE that resulted in death, was life-threatening, required hospitalization (or prolongation of existing hospitalization), or was an important medical event. Drug-related SAEs or AEs are those events with relationship to study therapy of certain, probable or possible.AEs were graded using the National Cancer Institute (NCI) Common Toxicity Criteria (CTC), v3: Grade 1=mild, 2=moderate, 3=severe, 4=life threatening, 5=death.Participants who discontinued the study due to any drug-related AEs were also recorded.
Measured: From start of study drug therapy up to 30 days after the last dose.
Most Frequent Drug-related Adverse Events (AEs)
Most frequent drug-related AEs are those AEs with frequency >=25% in either group. Drug-related AEs are those events with relationship to study therapy of certain, probable or possible.
Measured: From start of study drug therapy up to 30 days after the last dose.
Number of Participants With Grade 3 or 4 Abnormalities in Hematology Measurements
Abnormalities were graded according to the NCI CTC, version 3.0: Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = life threatening. Grades 3 and 4 criteria are defined as follows: Granulocytes: Grade 3 <1.0 - 0.5 x 10^9/L; Grade 4, <0.5 x 10^9/L. Hemoglobin: Grade 3, <8.0 - 6.5 g/dL; Grade 4, <6.5 g/dL. Platelets: Grade 3, <50.0 - 25.0 x 10^9/L; Grade 4, <25.0 x 10^9/L. Leukocytes: Grade 3, <2.0 - 1.0 x 10^9/L; Grade 4, <1.0 x 10^9/L.
Measured: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Abnormalities (Grade 1 or 2) in Prothrombin Time (PT)
PT is a measure of the clotting ability of the blood. Abnormalities were graded according to the NCI CTC, version 3.0: Grade 1=mild, Grade 2=moderate, Grade 3=severe, Grade 4=life-threatening and 5=death.
Measured: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Abnormalities (Grade 1 or 2) in Partial Thromboplastin Time (PTT)
PTT is a measure of the clotting ability of the blood. Abnormalities were graded according to the NCI CTC, version 3.0: Grade 1=mild, Grade 2=moderate, Grade 3=severe, Grade 4=life-threatening and 5=death.
Measured: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Grade 3 or 4 Serum Chemistry Abnormalities in Alanine Aminotransferase (ALT), Aspartate Aminotransferase (AST) and Alkaline Phosphatase
Abnormalities were graded according to the NCI CTC, version 3.0: Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = life threatening. Grade 3 and 4 criteria are defined as follows: ALT, AST and alkaline phosphatase: Grade 3: >5-20 x upper limit of normal (ULN), Grade 4: >20 x ULN.
Measured: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Grade 3 or 4 Serum Chemistry Abnormalities in Calcium, Potassium, Magnesium and Sodium
Abnormalities were graded according to the NCI CTC, version 3.0: Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = life threatening. Grade 3 and 4 criteria are defined as follows: Calcium: Grade 3-4 : <6.0 - <7.0 or >12.5 - >13.5 mg/dL, Potassium: Grade 3-4 : <2.5 - <3.0 or >6.0 - >7.0 mEq/L, Magnesium: Grade 3-4 : <0.6 - <0.8 or >2.46 - >6.6 mEq/L, Sodium:< 120- 130 or >155 - >160 mEq/L.
Measured: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Grade 3 or 4 Serum Chemistry Abnormalities in Creatinine, Bicarbonate, Inorganic Phosphorous and Bilirubin (Total).
Abnormalities were graded according to the NCI CTC, version 3.0: Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = life threatening. Grade 3 and 4 criteria are defined as follows: Creatinine: Grade 3-4 : > 3.0 -6.0 ULN (upper limit of normal),Bicarbonate: Grade 3-4: <16 -<22 mEq/L, Phosphorous: Grade 3-4 : <1.0 - <2.0 mg/dL, Bilirubin, total: Grade 3-4: >3.0 - >10.0 ULN.
Measured: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Identified Electrocardiogram (ECG) Abnormalities
ECGs were performed and all recordings were evaluated by the investigator. Abnormalities, if present at any study time point, were listed. The following ECG variables were collected: heart rate, PR interval, QRS width, and QT interval. Abnormalities in ECGs were defined by reference to institutional reports.
Measured: Baseline, Weeks 3, 9, 17 and 25, then every 8 weeks until the end of study treatment (up to 17 weeks).
Number of Participants With Abnormal Vital Signs Measurements
Vital signs included systolic and diastolic blood pressure and heart rate. The investigator used his or her judgement to decide whether or not the values were abnormal.
Measured: At each study visit (Week 3, 5, 7, 9, 13, 17 and 25) and end of treatment (up to 17 weeks)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Sep 2006 (estimated)
- Study startDec 2006
- Primary completionSep 2008
- Study completionSep 2008
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.
- Other trials for Breast CancerStudies of the same condition, open and under way.
- More trials run by Bristol-Myers SquibbThe 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
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 55 participants (actual)
Sponsor and investigators
- Lead sponsor
- Bristol-Myers Squibb
- Sponsor type
- Industry (pharma, biotech, devices)
- Investigators
- Bristol-Myers Squibb, Study director, Bristol-Myers Squibb
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00371254
- Sponsor's protocol ID
- CA180-059
- Status last verified
- Feb 2011
- First submitted
- 1 Sep 2006
- Last updated
- 15 Mar 2011
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 15 Mar 2011. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Phase II Study of Dasatinib (BMS-354825) for Advanced 'Triple-negative' Breast Cancer
- ClinicalTrials.gov ID
- NCT00371254
- Acronym / sponsor ID
- CA180-059
- Conditions
- Breast Cancer, Metastasis
- Keywords
- Recurrent, locally-advanced, or 'triple negative' metastatic breast cancer
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 55 participants (actual)
- Lead sponsor
- Bristol-Myers SquibbIndustry (pharma, biotech, devices)
- Study start
- Dec 2006
- Primary completion
- Sep 2008 (actual)
- Study completion
- Sep 2008 (actual)
- First posted
- 4 Sep 2006 (estimated)
- Results
- Posted 15 Mar 2011
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study will determine whether the investigational drug dasatinib is effective in treatment of women with progressive advanced triple-negative breast cancer.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 1 | Experimental | Drug: Dasatinib |
| 2 | Experimental | Drug: Dasatinib |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- females, 18 or older
- recurrent or progressive locally advanced, or 'triple negative' metastatic breast cancer
- paraffin-embedded tissue block must be available
- measurable disease
- prior chemotherapy with an anthracycline, a taxane, or both (neoadjuvant, adjuvant, or metastatic setting)
Key exclusion criteria (4 listed)
- Metastatic disease confined to bone only
- Symptomatic CNS metastasis
- Concurrent medical condition which may increase the risk of toxicity
- Unable to take oral medication
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 |
|---|---|---|
| DasatinibAlso: Sprycel, BMS-354825Tablets, Oral, 100 mg, twice daily as long as the patient benefits (avg <6 months) | Drug | 1 |
| DasatinibTablets, Oral, 70 mg, twice daily as long as the patient benefits (avg <6 months) | Drug | 2 |
Primary outcome
Number of Participants With Complete Response (CR) or Partial Response (PR)
Time frame: Baseline to end of study drug therapy (up to 65 weeks).
Tumor response was defined as the number of participants whose best response was CR or PR, per the Response Evaluation Criteria in Solid Tumor (RECIST): CR: disappearance of all target/non-target lesions; PR: >= 30% decrease in the sum of the LDs of target lesions relative to the baseline sum LD.
Percentage of Participants With Complete Response (CR) or Partial Response (PR)
Time frame: Baseline to end of study drug therapy (up to 65 weeks).
The percentage of participants whose best response was CR or PR, per the RECIST: CR: disappearance of all target/non-target lesions; PR: >= 30% decrease in the sum of the LDs of target lesions relative to the baseline sum LD.
21 secondary outcomes
Number of Participants With Complete Response (CR), Partial Response (PR) or Stable Disease (SD) at or After 16 Weeks on Study
Time frame: Baseline to 16 weeks.
Percentage of Participants With Complete Response (CR), Partial Response (PR) or Stable Disease (SD) at or After 16 Weeks on Study
Time frame: Baseline to 16 weeks
Proportion of Participants With Progression-Free Survival (PFS) at Weeks 9, 17, and 25
Time frame: Weeks 9, 17, and 25
Mean Number of Weeks of Complete Response (CR) or Partial Response (PR)
Time frame: Baseline to end of study drug therapy (up to 53.86 weeks)
Mean Plasma Concentration at Week 3
Time frame: At pre-dose and 1, 3, 6 and 12 hours after each dose administration
Mean Plasma Concentration at Week 7
Time frame: At pre-dose and 1, 3, 6 and 12 hours after each dose administration
Mean Change in Concentration of Collagen Type IV From Baseline
Time frame: Baseline, Week 3 and Week 5
Mean Change in Concentration of Vascular Endothelial Growth Factor Receptor-2 (VEGFR2) From Baseline
Time frame: Baseline, Week 3 and Week 5
Percentage Change in Tumor Biomarkers
Time frame: Baseline
Profiling of Messenger-ribonucleic Acid (mRNA) Expression: mRNA Signal Intensity
Time frame: Baseline
Number of Participants Who Died, Experienced Other Serious Adverse Events (SAEs) or Adverse Events (AEs)
Time frame: From start of study drug therapy up to 30 days after the last dose.
Number of Participants Who Experienced Drug-related SAEs, Drug-related AEs, Drug-related Grade 3 AEs and Discontinuations Due to Drug-related AEs
Time frame: From start of study drug therapy up to 30 days after the last dose.
Most Frequent Drug-related Adverse Events (AEs)
Time frame: From start of study drug therapy up to 30 days after the last dose.
Number of Participants With Grade 3 or 4 Abnormalities in Hematology Measurements
Time frame: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Abnormalities (Grade 1 or 2) in Prothrombin Time (PT)
Time frame: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Abnormalities (Grade 1 or 2) in Partial Thromboplastin Time (PTT)
Time frame: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Grade 3 or 4 Serum Chemistry Abnormalities in Alanine Aminotransferase (ALT), Aspartate Aminotransferase (AST) and Alkaline Phosphatase
Time frame: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Grade 3 or 4 Serum Chemistry Abnormalities in Calcium, Potassium, Magnesium and Sodium
Time frame: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Grade 3 or 4 Serum Chemistry Abnormalities in Creatinine, Bicarbonate, Inorganic Phosphorous and Bilirubin (Total).
Time frame: Throughout study, from start of study drug therapy up to 30 days after the last dose.
Number of Participants With Identified Electrocardiogram (ECG) Abnormalities
Time frame: Baseline, Weeks 3, 9, 17 and 25, then every 8 weeks until the end of study treatment (up to 17 weeks).
Number of Participants With Abnormal Vital Signs Measurements
Time frame: At each study visit (Week 3, 5, 7, 9, 13, 17 and 25) and end of treatment (up to 17 weeks)
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Mar 2011.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
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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.
Bristol-Myers Squibb study director
Bristol-Myers Squibb
10 sites in 4 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Dasatinib in people with Breast Cancer and Metastasis, run by Bristol-Myers Squibb at 10 sites in 4 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 7 inclusion and 4 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 15 Mar 2011. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 10 sites in United States, France, Spain, Italy. 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 15 Mar 2011). 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?
Number of Participants With Complete Response (CR) or Partial Response (PR) (time frame: Baseline to end of study drug therapy (up to 65 weeks).). The study lists 2 primary outcomes in all. 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 15 Mar 2011.