Rheumatoid ArthritisNCT01705730
A Non-Interventional Study of Rheumatoid Arthritis Patients Treated With RoActemra/Actemra (Tocilizumab) in Monotherapy
An observational study of Rheumatoid Arthritis, run by Hoffmann-La Roche at 17 sites in Belgium.
Trial summary
This observational study will evaluate the use and efficacy of RoActemra/Actemra (tocilizumab) in monotherapy in routine clinical practice in participants with rheumatoid arthritis. Eligible participants initiated on RoActemra/Actemra treatment according to the licensed label will be followed for 6 months. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Rheumatoid Arthritis
- What is being tested?
- tocilizumab
- How many people
- 71 participants
- Where
- 17 sitesBelgium
- Study dates
- 31 Jul 2012to 12 Dec 2014
- Phase
- Observational
- 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
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Participants with rheumatoid arthritis initiating treatment with RoActemra/Actemra in monotherapy
Who may be able to join
- Adult participants, >/= 18 years of age
- Moderate to severe rheumatoid arthritis according to the revised (1987) ACR criteria
- Participants in whom the treating physician has made the decision to commence RoActemra/Actemra treatment in monotherapy in accordance with the local label and the reimbursement criteria indicating that RoActemra/Actemra can be given in monotherapy in case of methotrexate intolerance or where continued treatment with methotrexate is inappropriate; this can include participants who have received RoActemra/Actemra treatment within 8 weeks prior to the enrolment visit
- Concomitant treatment with NSAIDs and/or corticosteroids is allowed
Who cannot join
- Participants who have received RoActemra/Actemra more than 8 weeks prior to the enrolment visit
- Participants who have previously received RoActemra/Actemra in a clinical trial or for compassionate use
- Participants receiving concomitant DMARD treatment for rheumatoid arthritis at baseline (e.g. hydroxychloroquine, sulfasalazine, methotrexate, leflunomide, gold compounds, cyclosporine) will be excluded from the study
- Participants who have received treatment with an investigational agent within 4 weeks (or 5 half-lives of the investigational agent, whichever is longer) before starting treatment with RoActemra/Actemra
- Participants with a history of autoimmune disease or any joint inflammatory disease other than rheumatoid arthritis
Trial locations and contacts
17 sites in 1 country.
17 sites in 1 country
Belgium17 sites
ASZ Aalst
Aalst, 9300
CH EpiCURA Site Ath
Ath, 7800
CHU Brugmann (Victor Horta)
Brussels, 1020
Hospital Erasme; Neurologie
Brussels, 1070
Reumaclinic
Genk, 3600
GHdC Site Saint-Joseph
Gilly (Charleroi), 6000
Clinique Notre Dame de Grâce
Gosselies, 6041
CH Jolimont - Lobbes (Jolimont)
Haine-Saint-Paul, 7100
AZ Groeninge
Kortrijk, 8500
Chr de La Citadelle
Liège, 4000
Clinique Saint-Joseph
Liège, 4000
CHU Ambroise Paré
Mons, 7000
AZ Damiaan
Ostend, 8400
Clinique St Pierre asbl
Ottignies, 1340
AZ Delta (Campus Wilgenstraat)
Roeselare, 8800
AZ Turnhout Sint Jozef
Turnhout, 2300
Sint Augustinus Wilrijk
Wilrijk, 2610
About this study
Official title: Mon-ACT: A Multi-center, Non-interventional Study in Rheumatoid Arthritis (RA) Patients Treated With Tocilizumab in Monotherapy
This observational study will evaluate the use and efficacy of RoActemra/Actemra (tocilizumab) in monotherapy in routine clinical practice in participants with rheumatoid arthritis. Eligible participants initiated on RoActemra/Actemra treatment according to the licensed label will be followed for 6 months.
- Conditions
- Rheumatoid Arthritis
- Being tested
- tocilizumab
- Medical subject headings
- Arthritis, Rheumatoid
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
tocilizumabDrug
Also called Actemra
Participants received tocilizumab monotherapy according to individualized physician-prescribed regimens.
| Study group | Role | What they receive |
|---|---|---|
| Tocilizumab | Participants with rheumatoid arthritis (RA) received tocilizumab monotherapy according to individualized physician-prescribed regimens. Receives: Drug: tocilizumab |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants on Tocilizumab Treatment at Month 6 After Treatment Initiation
Measured: Month 6 after treatment initiation
Secondary outcomes (34)
Percentage of Participants With Systemic Manifestations of RA at Baseline
Systemic manifestations of RA included anemia, fatigue, conventional risk factors for cardiovascular disease, C-Reactive Protein (CRP) above upper limit of normal, rheumatoid nodules, rheumatoid vasculitis and interstitial lung disease. Participants were included if they experienced at least any one of the conditions.
Measured: Baseline
Number of Participants With Disease-Modifying Antirheumatic Drugs (DMARDs) Intolerance and Inadequate Response
Measured: Baseline
Number of Participants With Inadequate Response to Other Biologics
Measured: Baseline
Time to Addition of Disease-Modifying Anti-rheumatic Drugs (DMARDs)
The time to DMARD addition equals to the time (days) between tocilizumab start and first start date of DMARDs.
Measured: Month 6
Percentage of Participants Who Had DMARDs During Study
Measured: Month 6
Number of Participants With Dose Reductions
Measured: 6 months
Number of Participants With Starting Tocilizumab After Failing DMARDs
Measured: Baseline
Number of Participants With Starting Tocilizumab After Stopping Other Biologic Agents
Measured: Baseline
Time to Reduction/Withdrawal of Corticosteroids
Measured: Month 6
Number of Dose Modifications Per Participant at Month 6
Number of dose modification per participant at Month 6 was reported.
Measured: Month 6
Mean Dosing Interval Per Participant at Month 6
Measured: Month 6
Percentage of Participants Discontinued From Tocilizumab for Safety Versus Efficacy
Measured: Month 6
Time for Restoration of Initial Dosing Regimen
Measured: Month 6
Percentage of Participants Who Were Not Adhering to Recommended Dosing Regimen
Measured: Month 6
Number of Participants Who Were Not Adhering to Recommended Management of AEs
Measured: Month 6
Percentage of Participants Still on Tocilizumab Monotherapy at Month 6
Measured: Month 6
Percentage of Participants With Reason for Choice of Monotherapy at Baseline
Measured: Baseline
Tender Joint Count (TJC)
TJC was determined by examining 28 and 68 joints and identifying the joints that were painful under pressure or to passive motion. Tenderness was recorded on the joint assessment form at baseline, no tenderness = 0, tenderness = 1.
Measured: Baseline, Month 3, 6
Swollen Joint Count (SJC)
SJC was determined by examining 28 and 66 joints and identifying when swelling was present. Swelling was recorded on the joint assessment form at baseline, no swelling = 0, swelling =1.
Measured: Baseline, Month 3, 6
Percentage of Participants With Disease Activity Score-28 (DAS28)
DAS28 was calculated from SJC and TJC using 28 joints count, erythrocyte sedimentation rate (ESR) (millimeter per hour [mm/hr]), and patient global assessment of disease activity (PGH) (measured on a 0 to 100 millimeter (mm) Visual Analogue Scale (VAS) where 0=no disease activity and 100=worst disease activity). DAS28 is a measurement of RA activity on a 0 to 10 scale: a score greater than (>) 5.1 indicates high disease activity; a score between 3.2 and 5.1 indicates moderate disease activity; a score of less than 3.2 indicates low disease activity; a score of less than (<) 2.6 is considered remission.
Measured: Baseline, Month 3, 6
Percentage of Participants With Good European League Against Rheumatism (EULAR) Response at Month 3 and Month 6
Clinical response assessed as per EULAR categorical DAS28 response criteria was defined as clinically meaningful improvement at a particular time point. EULAR response was based on change from baseline (CFB) in the DAS28 score and also on the actual DAS28 score at the time point so was more reflective of the current status of the participant. EULAR Good response: DAS28 <=3.2 and a CFB <-1.2. EULAR Moderate response: DAS28 >3.2 to ≤ 5.1 or a CFB < -0.6 to ≥ -1.2. EULAR No response: DAS28 ≤3.2 or CFB greater than or equal to (>=) -0.6, DAS28 >3.2 to <=5.1 or CFB>=-0.6 and DAS28 >5.1 or CFB >=-0.6. The DAS28 score was a measure of the participant's disease activity, based on the TJC (28 joints), SJC (28 joints), PGH, and ESR. DAS28 total scores ranged from 0 to approximately 10. Scores <2.6 = best disease control and scores >5.1 = worse disease control. A negative CFB indicated clinically meaningful improvement.
Measured: Month 3, 6
Percentage of Participants With American College of Rheumatology (ACR) Response at Month 3 and Month 6
ACR response was calculated based on total joint count evaluation (28 or 66/68 joint count) and other clinical and laboratory assessments. A positive ACR20 response required at least a 20% improvement (reduction) compared to baseline in swollen joint count (66 joints) and tender joint count (68 joints) and at least 3 of the following 5 assessments: patient's global assessment of pain, PGH, PhGH (all 3 assessed at 0 [good] to 100 mm [worst] VAS scale), participant assessment of disability measured by the Health Assessment Questionnaire-Disability Index (HAQ-DI) (assessed on a 0 to 3 scale, where higher scores represented higher disease activity), Acute phase reactant (CRP or ESR). A reduction in the level of and acute phase reactants was considered an improvement. ACR50, ACR70, ACR90 require a 50%, 70%, 90% improvement from baseline respectively.
Measured: Month 3, 6
Percentage of Participants With Disease Activity According to Clinical Disease Activity Index (CDAI) Response
CDAI is the numerical sum of 4 outcome parameters: TJC and SJC based on a 28-joint assessment, PGH and physician global assessment of disease activity (PhGH) assessed on 0-10 cm VAS; 0 = no disease activity and 10 = worst disease activity. CDAI total score = 0-76. CDAI <= 2.8 indicates clinical remission, >2.8 to 10 = low disease activity, >10 to 22 = moderate disease activity, and >22 = high (or severe) disease activity.
Measured: Baseline, Month 3, 6
Percentage of Participants With Disease Activity According to Simplified Disease Activity Index (SDAI) Response
The SDAI was a combined index for measuring disease activity in RA which reflected the numerical sum of five outcome parameters: TJC and SJC based on a 28-joint assessment, PGH and PhGH, assessed on 0-100 mm VAS where 0 = no disease activity and 100 = worst disease activity, and C-reactive protein (CRP). SDAI total score = 0-86. A SDAI score </= 3.3 represented clinical remission, a score of between 3.4 and 11.0 represented low disease activity, a score between 11 and 26.0 represented moderate disease activity and a score > 26.0 represented high (or severe) disease.
Measured: Baseline, Month 3, 6
Change From Baseline in Patient's Global Assessment of Disease Activity at Month 3 and Month 6
The Patient Global Assessment of disease activity provides an overall assessment of how RA affects the participant using a visual analogue score, where 0 indicates they are managing very well and 100 indicates they are managing very poorly. A decrease in the score indicates improvement.
Measured: Baseline, Month 3, 6
Change From Baseline in Physician Global Assessment of Disease Activity at Month 3 and Month 6
The physician's global assessment of disease activity was assessed using a 0 to 100 mm horizontal VAS by the physician. The left-hand extreme of the line equals 0 mm, and is described as "no disease activity" (symptom-free and no arthritis symptoms) and the right-hand extreme equals 100 mm, as "maximum disease activity" (maximum arthritis disease activity). A negative change from Baseline indicated improvement.
Measured: Baseline, Month 3, 6
Change From Baseline in Health Assessment Questionnaire (HAQ) at Month 3 and Month 6
The HAQ was a participant self-reported questionnaire for assessing the extent of a participant's functional ability. It consisted of 20 questions in 8 categories (dressing and grooming, rising, eating, walking, reach, grip, hygiene, and carrying out daily activities). Each question had 4 response options, ranging from 0=no difficulty; 1=some difficulty; 2=much difficulty; 3=unable to do. The HAQ scale was an average of all the scores and ranged from 0 to 3, where higher scores represented higher disease activity.
Measured: Baseline, Month 3, 6
Change From Baseline in VAS-Fatigue at Month 3 and Month 6
The VAS-fatigue provides an overall assessment of the level of fatigue that the participant is experiencing using a visual analogue score, where 0 indicates no fatigue and 100 indicates extreme fatigue. A decrease in the score indicates improvement.
Measured: Baseline, Month 3, 6
Change From Baseline in Patient's Global Assessment of Pain at Month 3 and Month 6
The Patient Global Assessment of pain provides an overall assessment of the severity of pain that the participant is experiencing using a visual analogue score, where 0 indicates no pain and 100 indicates unbearable pain. A decrease in the score indicates improvement.
Measured: Baseline, Month 3, 6
Change From Baseline in VAS-Morning Stiffness at Month 3 and Month 6
Morning stiffness was defined by the time elapsed between the time of usual awakening (even if not in the morning) and the time the participant was as limber as he/she would be during a day involving typical activities. Morning stiffness was assessed on a 100 mm VAS, where 0= none and 100= very severe.
Measured: Baseline, Month 3, 6
Percentage of Participants With an Adverse Event (AEs), Serious Adverse Events (SAEs), AEs of Special Interest (AESIs)
An AE was considered any unfavorable and unintended sign, symptom, or disease associated with the use of the study drug, whether or not considered related to the study drug. An Serious Adverse Events (SAEs) is any untoward medical occurrence that, at any dose, results in death, is life threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, or results in a congenital anomaly/birth defect. AESI included- serious/medically significant infections; myocardial Infarction/acute coronary syndrome; gastrointestinal perforations; malignancies; anaphylaxis/hypersensitivity reactions; demyelinating disorders; stroke; serious/medically significant bleeding events; serious/medically significant hepatic events.
Measured: Month 6
Percentage of Participants With AEs Leading to Dose Modifications
Measured: Month 6
C-reactive Protein (CRP]) Level
CRP is an acute phase reactant and is a measure of inflammation.
Measured: Baseline, Month 3, 6
Erythrocyte Sedimentation Rate (ESR) Level
ESR is an acute phase reactant and is a measure of inflammation.
Measured: Baseline, Month 3, 6
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Oct 2012 (estimated)
- Study start31 Jul 2012
- Primary completion12 Dec 2014
- Study completion12 Dec 2014
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 Rheumatoid ArthritisStudies of the same condition, open and under way.
- More trials run by Hoffmann-La RocheThe 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 71 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hoffmann-La Roche
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Clinical Trials, Study director, Hoffmann-La Roche
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01705730
- Sponsor's protocol ID
- ML28269
- Status last verified
- Aug 2018
- First submitted
- 10 Oct 2012
- Last updated
- 4 Sep 2018
- Results posted
- Yes, on ClinicalTrials.gov
Study at a glance
From the registry record, last updated by the sponsor on 4 Sep 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Mon-ACT: A Multi-center, Non-interventional Study in Rheumatoid Arthritis (RA) Patients Treated With Tocilizumab in Monotherapy
- ClinicalTrials.gov ID
- NCT01705730
- Acronym / sponsor ID
- ML28269
- Conditions
- Rheumatoid Arthritis
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 71 participants (actual)
- Lead sponsor
- Hoffmann-La RocheIndustry (pharma, biotech, devices)
- Study start
- 31 Jul 2012 (actual)
- Primary completion
- 12 Dec 2014 (actual)
- Study completion
- 12 Dec 2014 (actual)
- First posted
- 12 Oct 2012 (estimated)
- Results
- Posted 4 Sep 2018
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This observational study will evaluate the use and efficacy of RoActemra/Actemra (tocilizumab) in monotherapy in routine clinical practice in participants with rheumatoid arthritis. Eligible participants initiated on RoActemra/Actemra treatment according to the licensed label will be followed for 6 months.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Tocilizumab | – | Drug: tocilizumabParticipants with rheumatoid arthritis (RA) received tocilizumab monotherapy according to individualized physician-prescribed regimens. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Participants with rheumatoid arthritis initiating treatment with RoActemra/Actemra in monotherapy
Key inclusion criteria (4 listed)
- Adult participants, >/= 18 years of age
- Moderate to severe rheumatoid arthritis according to the revised (1987) ACR criteria
- Participants in whom the treating physician has made the decision to commence RoActemra/Actemra treatment in monotherapy in accordance with the local label and the reimbursement criteria indicating that RoActemra/Actemra can be given in monotherapy in case of methotrexate intolerance or where continued treatment with methotrexate is inappropriate; this can include participants who have received RoActemra/Actemra treatment within 8 weeks prior to the enrolment visit
- Concomitant treatment with NSAIDs and/or corticosteroids is allowed
Key exclusion criteria (5 listed)
- Participants who have received RoActemra/Actemra more than 8 weeks prior to the enrolment visit
- Participants who have previously received RoActemra/Actemra in a clinical trial or for compassionate use
- Participants receiving concomitant DMARD treatment for rheumatoid arthritis at baseline (e.g. hydroxychloroquine, sulfasalazine, methotrexate, leflunomide, gold compounds, cyclosporine) will be excluded from the study
- Participants who have received treatment with an investigational agent within 4 weeks (or 5 half-lives of the investigational agent, whichever is longer) before starting treatment with RoActemra/Actemra
- Participants with a history of autoimmune disease or any joint inflammatory disease other than rheumatoid arthritis
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 |
|---|---|---|
| tocilizumabAlso: ActemraParticipants received tocilizumab monotherapy according to individualized physician-prescribed regimens. | Drug | Tocilizumab |
Primary outcome
Percentage of Participants on Tocilizumab Treatment at Month 6 After Treatment Initiation
Time frame: Month 6 after treatment initiation
34 secondary outcomes
Percentage of Participants With Systemic Manifestations of RA at Baseline
Time frame: Baseline
Number of Participants With Disease-Modifying Antirheumatic Drugs (DMARDs) Intolerance and Inadequate Response
Time frame: Baseline
Number of Participants With Inadequate Response to Other Biologics
Time frame: Baseline
Time to Addition of Disease-Modifying Anti-rheumatic Drugs (DMARDs)
Time frame: Month 6
Percentage of Participants Who Had DMARDs During Study
Time frame: Month 6
Number of Participants With Dose Reductions
Time frame: 6 months
Number of Participants With Starting Tocilizumab After Failing DMARDs
Time frame: Baseline
Number of Participants With Starting Tocilizumab After Stopping Other Biologic Agents
Time frame: Baseline
Time to Reduction/Withdrawal of Corticosteroids
Time frame: Month 6
Number of Dose Modifications Per Participant at Month 6
Time frame: Month 6
Mean Dosing Interval Per Participant at Month 6
Time frame: Month 6
Percentage of Participants Discontinued From Tocilizumab for Safety Versus Efficacy
Time frame: Month 6
Time for Restoration of Initial Dosing Regimen
Time frame: Month 6
Percentage of Participants Who Were Not Adhering to Recommended Dosing Regimen
Time frame: Month 6
Number of Participants Who Were Not Adhering to Recommended Management of AEs
Time frame: Month 6
Percentage of Participants Still on Tocilizumab Monotherapy at Month 6
Time frame: Month 6
Percentage of Participants With Reason for Choice of Monotherapy at Baseline
Time frame: Baseline
Tender Joint Count (TJC)
Time frame: Baseline, Month 3, 6
Swollen Joint Count (SJC)
Time frame: Baseline, Month 3, 6
Percentage of Participants With Disease Activity Score-28 (DAS28)
Time frame: Baseline, Month 3, 6
Percentage of Participants With Good European League Against Rheumatism (EULAR) Response at Month 3 and Month 6
Time frame: Month 3, 6
Percentage of Participants With American College of Rheumatology (ACR) Response at Month 3 and Month 6
Time frame: Month 3, 6
Percentage of Participants With Disease Activity According to Clinical Disease Activity Index (CDAI) Response
Time frame: Baseline, Month 3, 6
Percentage of Participants With Disease Activity According to Simplified Disease Activity Index (SDAI) Response
Time frame: Baseline, Month 3, 6
Change From Baseline in Patient's Global Assessment of Disease Activity at Month 3 and Month 6
Time frame: Baseline, Month 3, 6
Change From Baseline in Physician Global Assessment of Disease Activity at Month 3 and Month 6
Time frame: Baseline, Month 3, 6
Change From Baseline in Health Assessment Questionnaire (HAQ) at Month 3 and Month 6
Time frame: Baseline, Month 3, 6
Change From Baseline in VAS-Fatigue at Month 3 and Month 6
Time frame: Baseline, Month 3, 6
Change From Baseline in Patient's Global Assessment of Pain at Month 3 and Month 6
Time frame: Baseline, Month 3, 6
Change From Baseline in VAS-Morning Stiffness at Month 3 and Month 6
Time frame: Baseline, Month 3, 6
Percentage of Participants With an Adverse Event (AEs), Serious Adverse Events (SAEs), AEs of Special Interest (AESIs)
Time frame: Month 6
Percentage of Participants With AEs Leading to Dose Modifications
Time frame: Month 6
C-reactive Protein (CRP]) Level
Time frame: Baseline, Month 3, 6
Erythrocyte Sedimentation Rate (ESR) Level
Time frame: Baseline, Month 3, 6
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Sep 2018.
- 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.
Clinical Trials study director
Hoffmann-La Roche
17 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Rheumatoid Arthritis, run by Hoffmann-La Roche at 17 sites in Belgium.
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 4 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 4 Sep 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 17 sites in Belgium. 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.
Are results available for this study?
Yes. Results are posted in the registry (first posted 4 Sep 2018). 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?
Percentage of Participants on Tocilizumab Treatment at Month 6 After Treatment Initiation (time frame: Month 6 after treatment initiation). 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 4 Sep 2018.