Multiple System AtrophyPhase 2NCT00977665
Clinical Trial to Assess Efficacy, Safety, and Tolerability of Rasagiline Mesylate 1 mg in Patients With Multiple System Atrophy of the Parkinsonian Subtype (MSA-P)
A Phase 2 study testing rasagiline mesylate in people with Multiple System Atrophy, run by Teva Branded Pharmaceutical Products R&D, Inc. at 47 sites in 12 countries.
Trial summary
To test the clinical effect of rasagiline on subjects with MSA of the parkinsonian subtype. Read more about this study
- Who is it for?
- Ages 30 years and older
- Conditions the study is for
- Multiple System Atrophy
- What is being tested?
- rasagiline mesylate
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 174 participants
- Where
- 47 sitesin 12 countries
- Study dates
- Dec 2009to Oct 2011
- 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 30 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Subjects over 30 years old with a diagnosis of Possible or Probable MSA of the parkinsonian subtype (MSA-P) according to The Gilman Criteria (2008).
- Subjects who are less than 3 years from the time of documented MSA diagnosis.
- Subjects with an anticipated survival of at least 3 years in the opinion of the investigator.
- Subjects who are willing and able to give informed consent. Subjects who are not able to write may give verbal consent in the presence of at least one witness, and the witness should sign the informed consent form.
Who cannot join
- Subjects receiving treatment with midodrine or other sympathomimetics within 4 weeks prior to baseline visit.
- Subjects with severe orthostatic symptoms as assessed by a score of ≥ 3 on Unified Multiple System Atrophy Rating Scale (UMSARS) question 9.
- Subjects who meet any of the following criteria which tend to suggest advanced disease:
- Speech impairment as assessed by a score of ≥ 3 on UMSARS question 1
- Swallowing impairment as assessed by a score of ≥ 3 on UMSARS question 2
- Impairment in ambulation as assessed by a score of ≥ 3 on UMSARS question 7
Show all 14Show fewer
- Falling more frequently than once per week as assessed by a score of ≥ 3 on UMSARS question 8
- Subjects taking disallowed medications according to the locally approved Azilect® label.
- Subjects taking monoamine oxidase (MAO) inhibitors within 3 months prior to baseline visit.
- Subjects with hypertension whose blood pressure, in the investigator's opinion, is not well controlled.
- Subjects who, based on the investigator's judgment, have a clinically significant or unstable medical or surgical condition that may preclude safe and complete study participation. Subjects with moderate or severe hepatic impairment.
- Subjects who have taken any investigational products within 60 days prior to baseline.
- Women of child-bearing potential who do not practice an acceptable method of birth control [acceptable methods of birth control in this study are: surgical sterilization, intrauterine devices, oral contraceptive, contraceptive patch, long-acting injectable contraceptive, partner's vasectomy, a double-protection method (condom or diaphragm with spermicide)].
- Pregnant or nursing women.
Trial locations and contacts
47 sites in 12 countries.
47 sites in 12 countries
United States15 sites
Teva Investigational Site 1003
Ann Arbor, Michigan
Teva Investigational Site 1061
Boca Raton, Florida
Teva Investigational Site 1001
Cleveland, Ohio
Teva Investigational Site 1005
Houston, Texas
Teva Investigational Site 1004
Irvine, California
Teva Investigational Site 1014
La Jolla, California
Teva Investigational Site 1013
Nashville, Tennessee
Teva Investigational Site 1002
Philadelphia, Pennsylvania
Teva Investigational Site 1007
Rochester, Minnesota
Teva Investigational Site 1008
Rochester, New York
Teva Investigational Site 1011
St Louis, Missouri
Teva Investigational Site 1006
Sunnyvale, California
Teva Investigational Site 1012
Tampa, Florida
Teva Investigational Site 1010
Washington D.C., District of Columbia
Teva Investigational Site 1009
Worcester, Massachusetts
Germany6 sites
Teva Investigational Site 3206
Dresden
Teva Investigational Site 3203
Kiel
Teva Investigational Site 3201
Marburg
Teva Investigational Site 3205
München
Teva Investigational Site 3204
Tübingen
Teva Investigational Site 3202
Ulm
Canada4 sites
Teva Investigational Site 1111
Greenfield Park, Quebec
Teva Investigational Site 1108
Montreal, Quebec
Teva Investigational Site 1109
Ottawa, Ontario
Teva Investigational Site 1110
Québec, Quebec
Hungary3 sites
Teva Investigational Site 5101
Budapest
Teva Investigational Site 5102
Debrecen
Teva Investigational Site 5103
Miskolc
Israel3 sites
Teva Investigational Site 8004
Haifa
Teva Investigational Site 8002
Ramat Gan, IL
Teva Investigational Site 8003
Tel Aviv
Italy3 sites
Teva Investigational Site 3006
Bologna
Teva Investigational Site 3004
Roma
Teva Investigational Site 3005
Venezia - Lido
Spain3 sites
Teva Investigational Site 3101
Barcelona
Teva Investigational Site 3102
Barcelona
Teva Investigational Site 3103
Seville
United Kingdom3 sites
Teva Investigational Site 3403
Cardiff, Wales
Teva Investigational Site 3401
London
Teva Investigational Site 3402
Newcastle upon Tyne
Austria2 sites
Teva Investigational Site 3305
Graz
Teva Investigational Site 3304
Innsbruck
France2 sites
Teva Investigational Site 3503
Lille
Teva Investigational Site 3502
Pessac
Netherlands2 sites
Teva Investigational Site 3801
Amersfoort
Teva Investigational Site 3802
Sittard-Geleen
About this study
Official title: A Multi-centered, Randomized, Double-blind, Placebo-controlled Clinical Trial to Assess the Efficacy, Safety, and Tolerability of Rasagiline Mesylate 1 mg in Patients With Multiple System Atrophy of the Parkinsonian Subtype (MSA-P)
To test the clinical effect of rasagiline on subjects with MSA of the parkinsonian subtype.
- Conditions
- Multiple System Atrophy
- Being tested
- rasagiline mesylate, placebo
- Medical subject headings
- Multiple System Atrophy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
rasagiline mesylateDrug
Also called Azilect, TVP-1012
rasagiline 1 mg tablet/day for 48 weeks
placeboDrug
placebo tablet for 48 weeks
| Study group | Role | What they receive |
|---|---|---|
| rasagiline mesylate | Experimental | rasagiline tablet, 1 mg/day for up to 48 weeks. Receives: Drug: rasagiline mesylate |
| placebo | Placebo comparator | placebo tablet for up to 48 weeks. Receives: Drug: placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change From Baseline to Week 48/Termination Visit in the Total Unified Multiple System Atrophy Rating Scale (UMSARS Part I and II)
This outcome represents the sum of 2 UMSARS sub-scales: Part I: Historical Review that includes 12 items and Part II: Motor Examination that includes 14 items. All items range from 0 to 4. Each subscale score is the sum of its items and the total UMSARS score is the sum of all 26 items. Hence the total UMSARS score can range from 0 to 104, with 0 meaning no impairment and 104 indicating severe impairment. Negative change from baseline scores indicate improvement.
In the case that 6 items or more (out of 26) were missing at a certain visit, the UMSARS score for that visit was assigned a missing value.
Measured: Day 0 (baseline), Week 48
Secondary outcomes (13)
Clinical Global Impression Improvement (CGI-I) at Week 48/Termination Visit
Outcome measures the investigator's clinical impression of the participants' improvement at Week 48 as compared to Week 12. CGI scale range from 1-7, with 1=very much improved, 4= no change, and 7=very much worse.
In order to maintain the overall (hypotheses about primary and key secondary endpoints) type I error at the 0.05 level an hierarchy will be employed as follows: If the primary endpoint will be found to be significant at a significance level of 0.05 then the first key secondary endpoint will be tested, if this endpoint will be found to be significant in a significance level of 0.05 then the second key secondary endpoint will be tested and so on. The 'key' secondary endpoints are outcomes 2-6.
Measured: Week 48
Change From Baseline to Week 24 in Total Unified Multiple System Atrophy Rating Scale (UMSARS) Score
The UMSARS is composed of 2 sub-scales: Part I: Historical Review that includes 12 items and Part II: Motor Examination that includes 14 items. All items range from 0 to 4. Each subscale score is the sum of its items and the total UMSARS score is the sum of all 26 items. Hence the total UMSARS score can range from 0 to 104, with 0 meaning no impairment and 104 indicating severe impairment. Negative change from baseline scores indicate improvement.
In the case that 6 items or more (out of 26) were missing at a certain visit, the UMSARS score for that visit was assigned a missing value.
Measured: Day 0 (baseline), Week 24
Percentage of Participants Who Achieved a Score of >=3 on the Unified Multiple System Atrophy Rating Scale (UMSARS) Question #7 Regarding Ambulation
UMSARS' Question #7 concerns the participant's ability to walk, rated on a scale of 0=normal to 4=cannot walk at all even with assistance. This endpoint counts participants rated a 3 or worse. Rating 3 = Severely impaired; assistance and/or walking aid needed occasionally.
Measured: up to week 48
Mean Score of the Composite Autonomic Symptom Scale Select (COMPASS_Select Change) at Week 48/Termination Visit
COMPASS_Select change is comprised of 5 of the 11 domains in the COMPASS scale: Orthostatic Intolerance, Bladder Disorder, Sweating, Vasomotor, and Sleep Disorder COMPASS_Select change has a range of -150 to 150, with -150 indicating symptoms are much better and 150 indicating symptoms are much worse.
Measured: 48 weeks
Change From Baseline to Week 48/Termination Visit in the Multiple System Atrophy (MSA) Health-related Quality of Life (QoL) Scale
The Multiple System Atrophy Quality of Life questionnaire (MSA-QoL) is a self-reported questionnaire focusing on MSA-specific symptoms and has a scale ranging from 0 - 160, with 0= 'no problem' and 160= "extreme problem".
Measured: Day 0 (baseline), Week 48
Rate of Progression in Total Unified Multiple System Atrophy Rating Scale (UMSARS) Score From Baseline to Weeks 12-48
The UMSARS is composed of 2 sub-scales: Part I: Historical Review that includes 12 items and Part II: Motor Examination that includes 14 items. All items range from 0 to 4. Each subscale score is the sum of its items and the total UMSARS score is the sum of all 26 items. Hence the total UMSARS score can range from 0 to 104, with 0 meaning no impairment and 104 indicating severe impairment.
The rate of progression of atrophy is represented by the slope of change from baseline scores for visits between Weeks 12 and 48.
Measured: Day 0 (baseline), Weeks 12-48
Change From Baseline to Week 48 or Termination in UMSARS Subscores for Parts I, II and IV
UMSARS Part I is an historical review and scores symptoms of neurological and autonomic dysfunction with 12 items rated on a scale of 0 (normal) to 4 (extreme dysfunction). The full scale for Part 1 is therefore 0 (normal) to 48 (extreme dysfunction). Part II is a motor examination and has 14 items also rated on a scale of 0 to 4 for a full scale of 0 (normal) to 56 (extreme dysfunction). Part IV is a global disability scale with rates the extent of disease from 1 (normal) to 5 (severe disease).
Measured: Day 0 (baseline), Week 48 or termination visit
Change From Baseline to Week 12 in Total UMSARS Score for Symptomatic Effect
This outcome represents the sum of 2 UMSARS sub-scales: Part I: Historical Review that includes 12 items and Part II: Motor Examination that includes 14 items. All items range from 0 to 4. Each subscale score is the sum of its items and the total UMSARS score is the sum of all 26 items. Hence the total UMSARS score can range from 0 to 104, with 0 meaning no impairment and 104 indicating severe impairment. Negative change from baseline scores indicate improvement.
Measured: Day 0 (baseline), Week 12
Estimates for Time to Change in Anti-Parkinsonian or Anti-Orthostatis Hypotension Medications
Change in anti-parkinsonian or anti-orthostatic hypotension medication is defined by at least one of the following events:
- An addition of a new anti-parkinsonian or anti-orthostatic hypotension medication during study.
- Dose modification of anti-parkinsonian or anti-orthostatic hypotension concomitant medications reflecting disease progression.
The event of interest, determined on a by patient basis, therefore, is the earliest event of the two events defined above. Otherwise, patient is right censored according to his/her study termination date.
Since less than 25% of participants had an event, median estimatation for time to change in medications is not possible.
Measured: Day 0 (baseline) to Week 48 or termination visit
Change From Baseline to Week 48 or Termination in the Montreal Cognitive Assessment Scale (MoCA) Scale
MoCA is a cognitive screening test which helps health professionals identify mild cognitive impairment. The total scale is 0 (significant cognitive impairment) to 30 (no impairment detected). Scores >=26 are considered normal. Positive change from baseline scores indicate improvement in cognition.
Measured: Day 0 (baseline), Week 48 or termination visit
Percentage of Participants Who Achieved a Score of >=3 on the Unified Multiple System Atrophy Rating Scale (UMSARS) Question #1 (Speech Impairment), Question #2 (Swallowing Impairment) and Question #8 (Falling)
UMSARS' questions are rated on a scale of 0=normal to 4=extreme impairment.
This endpoint reports the percentage of participants rated a 3 or worse. Rating 3 = Severely impaired speech (Question #1), swallowing (Question #2) or falling more frequently than once per week (Question #8).
Measured: up to week 48
Change From Baseline to Week 48 or Termination in the Beck Depression Inventory Scale (BDI-II)
The Beck Depression Inventory (BDI-II), is a 21-question multiple-choice self-report inventory, one of the most widely used instruments for measuring the severity of depression. Participants are asked to pick the answer for each question that best describes the way they have been feeling in the past two weeks, including the day participants complete the questionnaire. Each question is rated on a scale of 0-3, with 0 meaning the participant does not feel the emotion described in the question, and 3 meaning the participant has extremely strong feelings. Total scale is 0 (no evidence of depression) to 63 (extreme depression). Negative change from baseline scores indicate improvement in level of depression.
Measured: Day 0 (baseline), Week 48 or termination visit
Total Number of Falls During the Study
Participants recorded each time they fell during the study in a diary.
Measured: Day 1 up to week 48
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Sep 2009 (estimated)
- Study startDec 2009
- Primary completionOct 2011
- Study completionOct 2011
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 Multiple System AtrophyStudies of the same condition, open and under way.
- 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
- 174 participants (actual)
Sponsor and investigators
- Lead sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- H. Lundbeck A/S
- Responsible party
- Sponsor
- Investigators
- Werner Poewe, Prof, Principal investigator, Innsbruck Medical University, Innsbruck, Austria
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00977665
- Sponsor's protocol ID
- MSA-RAS-202
- Other IDs
- 2009-014644-11, 2009
- Status last verified
- Feb 2015
- First submitted
- 15 Sep 2009
- Last updated
- 26 Feb 2015
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
Publications
Poewe W, Seppi K, Fitzer-Attas CJ, Wenning GK, Gilman S, Low PA, Giladi N, Barone P, Sampaio C, Eyal E, Rascol O; Rasagiline-for-MSA investigators. Efficacy of rasagiline in patients with the parkinsonian variant of multiple system atrophy: a randomised, placebo-controlled trial. Lancet Neurol. 2015 Feb;14(2):145-52. doi: 10.1016/S1474-4422(14)70288-1. Epub 2014 Dec 8.
PubMed 25498732
Study at a glance
From the registry record, last updated by the sponsor on 26 Feb 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Multi-centered, Randomized, Double-blind, Placebo-controlled Clinical Trial to Assess the Efficacy, Safety, and Tolerability of Rasagiline Mesylate 1 mg in Patients With Multiple System Atrophy of the Parkinsonian Subtype (MSA-P)
- ClinicalTrials.gov ID
- NCT00977665
- Acronym / sponsor ID
- MSA-RAS-202
- Conditions
- Multiple System Atrophy
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 174 participants (actual)
- Lead sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.Industry (pharma, biotech, devices)
- Collaborators
- H. Lundbeck A/S
- Study start
- Dec 2009
- Primary completion
- Oct 2011 (actual)
- Study completion
- Oct 2011 (actual)
- First posted
- 16 Sep 2009 (estimated)
- Results
- Posted 26 Feb 2015
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To test the clinical effect of rasagiline on subjects with MSA of the parkinsonian subtype.
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 |
|---|---|---|
| rasagiline mesylate | Experimental | Drug: rasagiline mesylaterasagiline tablet, 1 mg/day for up to 48 weeks. |
| placebo | Placebo comparator | Drug: placeboplacebo tablet for up to 48 weeks. |
Who may qualify
- Ages
- 30 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Subjects over 30 years old with a diagnosis of Possible or Probable MSA of the parkinsonian subtype (MSA-P) according to The Gilman Criteria (2008).
- Subjects who are less than 3 years from the time of documented MSA diagnosis.
- Subjects with an anticipated survival of at least 3 years in the opinion of the investigator.
- Subjects who are willing and able to give informed consent. Subjects who are not able to write may give verbal consent in the presence of at least one witness, and the witness should sign the informed consent form.
Key exclusion criteria (14 listed)
- Subjects receiving treatment with midodrine or other sympathomimetics within 4 weeks prior to baseline visit.
- Subjects with severe orthostatic symptoms as assessed by a score of ≥ 3 on Unified Multiple System Atrophy Rating Scale (UMSARS) question 9.
- Subjects who meet any of the following criteria which tend to suggest advanced disease:
- Subjects taking disallowed medications according to the locally approved Azilect® label.
- Subjects taking monoamine oxidase (MAO) inhibitors within 3 months prior to baseline visit.
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 |
|---|---|---|
| rasagiline mesylateAlso: Azilect, TVP-1012rasagiline 1 mg tablet/day for 48 weeks | Drug | rasagiline mesylate |
| placeboplacebo tablet for 48 weeks | Drug | placebo |
Primary outcome
Change From Baseline to Week 48/Termination Visit in the Total Unified Multiple System Atrophy Rating Scale (UMSARS Part I and II)
Time frame: Day 0 (baseline), Week 48
This outcome represents the sum of 2 UMSARS sub-scales: Part I: Historical Review that includes 12 items and Part II: Motor Examination that includes 14 items. All items range from 0 to 4. Each subscale score is the sum of its items and the total UMSARS score is the sum of all 26 items. Hence the total UMSARS score can range from 0 to 104, with 0 meaning no impairment and 104 indicating severe impairment. Negative change from baseline scores indicate improvement. In the case that 6 items or more (out of 26) were missing at a certain visit, the UMSARS score for that visit was assigned a missing value.
13 secondary outcomes
Clinical Global Impression Improvement (CGI-I) at Week 48/Termination Visit
Time frame: Week 48
Change From Baseline to Week 24 in Total Unified Multiple System Atrophy Rating Scale (UMSARS) Score
Time frame: Day 0 (baseline), Week 24
Percentage of Participants Who Achieved a Score of >=3 on the Unified Multiple System Atrophy Rating Scale (UMSARS) Question #7 Regarding Ambulation
Time frame: up to week 48
Mean Score of the Composite Autonomic Symptom Scale Select (COMPASS_Select Change) at Week 48/Termination Visit
Time frame: 48 weeks
Change From Baseline to Week 48/Termination Visit in the Multiple System Atrophy (MSA) Health-related Quality of Life (QoL) Scale
Time frame: Day 0 (baseline), Week 48
Rate of Progression in Total Unified Multiple System Atrophy Rating Scale (UMSARS) Score From Baseline to Weeks 12-48
Time frame: Day 0 (baseline), Weeks 12-48
Change From Baseline to Week 48 or Termination in UMSARS Subscores for Parts I, II and IV
Time frame: Day 0 (baseline), Week 48 or termination visit
Change From Baseline to Week 12 in Total UMSARS Score for Symptomatic Effect
Time frame: Day 0 (baseline), Week 12
Estimates for Time to Change in Anti-Parkinsonian or Anti-Orthostatis Hypotension Medications
Time frame: Day 0 (baseline) to Week 48 or termination visit
Change From Baseline to Week 48 or Termination in the Montreal Cognitive Assessment Scale (MoCA) Scale
Time frame: Day 0 (baseline), Week 48 or termination visit
Percentage of Participants Who Achieved a Score of >=3 on the Unified Multiple System Atrophy Rating Scale (UMSARS) Question #1 (Speech Impairment), Question #2 (Swallowing Impairment) and Question #8 (Falling)
Time frame: up to week 48
Change From Baseline to Week 48 or Termination in the Beck Depression Inventory Scale (BDI-II)
Time frame: Day 0 (baseline), Week 48 or termination visit
Total Number of Falls During the Study
Time frame: Day 1 up to week 48
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Feb 2015.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 25498732Poewe W, Seppi K, Fitzer-Attas CJ, Wenning GK, Gilman S, Low PA, Giladi N, Barone P, Sampaio C, Eyal E, Rascol O; Rasagiline-for-MSA investigators. Efficacy of rasagiline in patients with the parkinsonian variant of multiple system atrophy: a randomised, placebo-controlled trial. Lancet Neurol. 2015 Feb;14(2):145-52. doi: 10.1016/S1474-4422(14)70288-1. Epub 2014 Dec 8.
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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.
Werner Poewe, Prof principal investigator
Innsbruck Medical University, Innsbruck, Austria
47 sites in 12 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing rasagiline mesylate in people with Multiple System Atrophy, run by Teva Branded Pharmaceutical Products R&D, Inc. at 47 sites in 12 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 4 inclusion and 14 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 26 Feb 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 47 sites in United States, Germany, Canada, Hungary, Israel and 7 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 26 Feb 2015). 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?
Change From Baseline to Week 48/Termination Visit in the Total Unified Multiple System Atrophy Rating Scale (UMSARS Part I and II) (time frame: Day 0 (baseline), Week 48). 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 NCT00977665, 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 26 Feb 2015.