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Multiple SclerosisPhase 3REFLEXIONNCT00813709

Long-term Follow-Up of Patients Who Participated in Study 27025 (REFLEX)

A Phase 3 study testing RNF in people with Multiple Sclerosis and Clinically Isolated Syndrome, run by Merck KGaA, Darmstadt, Germany at 57 sites in 24 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

REFLEXION is a double blind extension of the study 27025 (NCT00404352) (REFLEX). The purpose of the study is to obtain long-term follow-up data in subjects with clinically definite multiple sclerosis (MS) and subjects with a first demyelinating event at high risk of converting to MS, treated with fetal bovine serum… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
RNF
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
402 participants
Where
57 sitesin 24 countries
Study dates
Dec 2008to Sep 2013
Phase
Phase 3
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

Who may be able to join

  • Reach scheduled end of study in Study 27025 (REFLEX) (completion of 24 months participation)
  • Medical assessment by the Investigator/treating physician from study 27025 that there is no objection to the subject's participation in this extension trial considering the medical experience from Study 27025 (REFLEX). Special attention should be given to laboratory abnormalities and clinically significant liver, renal and bone-marrow dysfunction
  • If female, subject must:
  • be neither pregnant nor breast-feeding, nor attempting to conceive
  • use a highly effective method of contraception. A highly effective method of contraception is defined as those which result in a low failure rate (that is [i.e.] less than 1 percent [%] per year) when used consistently and correctly such as implants, injectables, combined oral contraceptives, some intrauterine devices (IUDs), sexual abstinence or vasectomized partner
  • Subject is willing to follow study procedures
  • Subject has given written informed consent

Who cannot join

  • Subject has any disease other than MS that could better explain the subject's signs and symptoms
  • Subject has a primary progressive course of MS
  • Subject has total bilirubin greater than 2.5 times upper limit of normal (ULN) at both Month 24 and at the previous visit (i.e. Month 21) (subjects with greater than 2.5 times ULN at Month 24 only are eligible for enrollment and should be managed as per label recommendations until normalization of the value)
  • Subject has total aspartate aminotransferase (AST) or alanine aminotransferase (ALT) or alkaline phosphatase (ALP) greater than 2.5 times the ULN values at both Month 24 and at the previous visit (i.e. Month 21) (subjects with greater than 2.5 times ULN at Month 24 only are eligible for enrollment and should be managed as per label recommendations until normalization of the value)
  • Subject suffers from another current autoimmune disease
  • Subject suffers from major medical or psychiatric illness (including history of, or current, severe depressive disorders and/or suicidal ideation) that in the opinion of the investigator creates undue risk to the subject or could affect compliance with the study protocol
Show all 16Show fewer
  • Subject has a history of seizures not adequately controlled by treatment
  • Subject has cardiac disease, such as angina, congestive heart failure or arrhythmia
  • Subject has a known allergy to IFN-beta or the excipient(s) of the study medication
  • Subject has any condition that could interfere with the MRI evaluation
  • Subject has a known allergy to gadolinium-diethylene triamine pentaacetic acid (DTPA)
  • Subject has a history of alcohol or drug abuse
  • Subject has previously participated in this study
  • Subject has moderate to severe renal impairment
  • Subject is pregnant or lactating
  • Subject has any medical, psychiatric or other conditions that compromise his/her ability to understand the subject information, to give informed consent, to comply with the study protocol, or to complete the study

Trial locations and contacts

57 sites in 24 countries.

57 sites in 24 countries

Russia7 sites
  • Research Site

    Moscow

  • Research Site

    Novosibirsk

  • Research Site

    Saint Petersburg

  • Research Site

    Samara

  • Research Site

    Saratov

  • Research Site

    Velikiy Novgorod

  • Research Site

    Yekaterinburg

Other trials in Russia

Bulgaria5 sites
  • Research Site

    Pleven

  • Research Site

    Rousse

  • Research Site

    Shumen

  • Research Site

    Sofia

  • Research Site

    Varna

Other trials in Bulgaria

Croatia5 sites
  • Research Site

    Karlovac

  • Research Site

    Osijek

  • Research Site

    Rijeka

  • Research Site

    Split

  • Research Site

    Zagreb

Other trials in Croatia

Poland4 sites
  • Research Site

    Bialystok

  • Research Site

    Lodz

  • Research Site

    Warsaw

  • Research Site

    Wroclaw

Other trials in Poland

Romania4 sites
  • Research Site

    Bucharest

  • Research Site

    Iași

  • Research Site

    Târgu Mureş

  • Research Site

    Timișoara

Other trials in Romania

Spain4 sites
  • Research Site

    Barcelona

  • Research Site

    Bilbao

  • Research Site

    Madrid

  • Research Site

    Seville

Other trials in Spain

Czechia3 sites
  • Research Site

    Hradec Králové

  • Research Site

    Olomouc

  • Research Site

    Prague

Other trials in Czechia

Belgium2 sites
  • Research Site

    Bruges

  • Research Site

    Leuven

Other trials in Belgium

Canada2 sites
  • Research Site

    Ontario

  • Research Site

    Victoria British Columbia

Other trials in Canada

Estonia2 sites
  • Research Site

    Tallinn

  • Research Site

    Tartu

Other trials in Estonia

France2 sites
  • Research Site

    Paris

  • Research Site

    Poissy

Other trials in France

Germany2 sites
  • Research Site

    Hanover

  • Research Site

    Henningsforf

Other trials in Germany

Israel2 sites
  • Research Site

    Safed

  • Research Site

    Tel HaShomer

Other trials in Israel

Italy2 sites
  • Research Site

    Milan

  • Research Site

    Padova

Other trials in Italy

Serbia2 sites
  • Reserch Site

    Belgrade

  • Research Site

    Niš

Other trials in Serbia

Argentina1 site
  • Research Site

    Mendoza

Other trials in Argentina

Austria1 site
  • Research Site

    Graz

Other trials in Austria

Finland1 site
  • Research Site

    Oulu

Other trials in Finland

Greece1 site
  • Research Site

    Athens

Other trials in Greece

Latvia1 site
  • Research Site

    Riga

Other trials in Latvia

Lebanon1 site
  • Research Site

    Beirut

Other trials in Lebanon

Morocco1 site
  • Research Site

    Rabat

Other trials in Morocco

Portugal1 site
  • Research Site

    Lisbon

Other trials in Portugal

Slovakia1 site
  • Research Site

    Prešov

Other trials in Slovakia

About this study

Official title: Double-blind Extension of the Study 27025 (REFLEX) to Obtain Long-term Follow-up Data in Patients With Clinically Definite MS and Patients With a First Demyelinating Event at High Risk of Converting to MS, Treated With Rebif® New Formulation (REFLEXION)

REFLEXION is a double blind extension of the study 27025 (NCT00404352) (REFLEX). The purpose of the study is to obtain long-term follow-up data in subjects with clinically definite multiple sclerosis (MS) and subjects with a first demyelinating event at high risk of converting to MS, treated with fetal bovine serum [FBS]-free/human serum albumin [HSA]-free formulation of interferon [IFN]-beta-1a (RNF).

Read the detailed description

The objective of the study is to investigate whether RNF treatment initiated after the first clinical event versus delayed treatment results in the prolongation of time to Clinically Definite Multiple Sclerosis (CDMS) conversion up to Month 36 and up to Month 60 since randomization in Study 27025 (REFLEX). Furthermore, the study is intended to explore whether RNF treatment initiated after the first clinical event versus delayed treatment delays disability (including development of secondary progressive MS) and reduces disease activity (including the annual relapse rate [ARR]) in the long term (up to Month 36 and up to Month 60 since randomization in Study 27025 (REFLEX). The study will also assess the long-term safety profile of RNF (up to Month 36 and up to Month 60 since randomization in Study 27025 (REFLEX).

Being tested
RNF, Placebo
Keywords
Interferon 1-beta, Clinical Definite Multiple Sclerosis
Medical subject headings
Multiple Sclerosis

What participants receive

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

  • RNFDrug

    Also called Rebif®

    Single dose of RNF will be administered subcutaneously three times weekly at least 48 hours apart at a starting dose of 8.8 microgram (mcg) for first 2 weeks followed by 22 mcg for next 2 weeks and finally 44 mcg until 60 months.

  • RNFDrug

    Also called Rebif®

    Single dose of RNF will be administered subcutaneously once weekly at a starting dose of 8.8 mcg for first 2 weeks followed by 22 mcg for next 2 weeks and finally 44 mcg until 60 months.

  • RNFDrug

    Also called Rebif®

    Participants who were initially randomized in Study 27025 (REFLEX) to the placebo treatment group will be switched to single dose of RNF administered subcutaneously three times weekly at least 48 hours apart at a dose of 8.8 mcg for first 2 weeks followed by 22 mcg for next 2 weeks and finally 44 mcg until 60 months.

  • PlaceboDrug

    Single dose matching placebo will be administered subcutaneously twice weekly. Placebo is supplied as a transparent, sterile solution for injection in pre-filled syringes matching the RNF pre-filled syringes, each containing 0.5 milliliter (mL).

Study groups in NCT00813709
Study groupRoleWhat they receive
RNF 44 mcg thrice weeklyActive comparatorNot described
Receives: Drug: RNF
RNF 44 mcg once weekly and placeboActive comparatorNot described
Receives: Drug: RNF; Drug: Placebo
Placebo/RNF 44 mcg thrice weeklyActive comparatorNot described
Receives: Drug: RNF

What is being measured

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

  1. Time to Conversion to Clinically Definite Multiple Sclerosis (CDMS) Defined by Either a Second Attack or a Sustained Increase (Greater Than or Equal to 1.5 Points) in the Expanded Disability Status Scale (EDSS) Score up to 36 Months

    CDMS was defined by the occurrence of a second attack or relapse over 36 months in participants who presented with clinically isolated syndrome (CIS) accompanied by an abnormal magnetic resonance imaging (MRI) scan. EDSS assesses disability in 8 functional systems. An overall score ranging from 0 (normal) to 10 (death due to multiple sclerosis [MS]) was calculated. Time to conversion to CDMS was represented by Kaplan-Meier estimates of the cumulative percentage (%) of participants with CDMS.

    Measured: Baseline (Day 1 of Study 27025) up to 36 Months

Secondary outcomes (23)
  1. Time to Confirmed Expanded Disability Status Scale (EDSS) Progression up to 36 Months

    EDSS assesses disability in 8 functional systems. An overall score ranging from 0 (normal) to 10 (death due to MS) was calculated. A confirmed EDSS progression was defined EDSS greater than or equal to 1.0 point confirmed during a visit performed 6 months later. Time to confirmed EDSS progression was represented by Kaplan-Meier estimates of the cumulative percentage (%) of participants with confirmed EDSS progression.

    Measured: Baseline (Day 1 of Study 27025) up to 36 Months

  2. Number of Combined Unique Active (CUA) Lesions, New Time Constant 2 (T2) Lesions, New Gadolinium Enhanced (Gd+) Lesions and New Time Constant 1 (T1) Lesions Per Participant Per Scan at Month 36

    Number of CUA lesions, new T2 lesions, new Gd+ lesions and new T1 lesions were measured by using MRI scans.

    Measured: Month 36

  3. Change From Baseline in Time Constant 1 (T1) Hypointense Lesion Volume and Time Constant 2 (T2) Lesion Volume at Month 36

    Change from baseline in lesion volume was measured by using MRI scans for T1 hypointense lesions and T2 lesions at Month 36

    Measured: Baseline (Day 1 of Study 27025), Month 36

  4. Percent Change From Baseline in Brain Volume at Month 36

    Percent change in brain volume was measured by using MRI scans.

    Measured: Baseline (Day 1 of Study 27025), Month 36

  5. Percentage of Participants With Conversion to McDonald Multiple Sclerosis (MS) up to 36 Months

    The McDonald criteria use dissemination in time and space established by MRI findings to provide a clinical diagnosis for MS. Dissemination in time is established by a new T2 or Gd+ lesion found on a repeat MRI. Dissemination in space is established by the presence of any 3 of the following: 1 Gd+ lesion or 9 T2 bright lesions if there is no enhancement; greater than or equal to 1 infratentorial lesion; greater than or equal to 1 juxtacortical lesion; greater than or equal to 3 periventricular lesions.

    Measured: Baseline (Day 1 of Study 27025) up to CDMS conversion and/or up to 36 Months

  6. Change From Baseline in Paced Auditory Serial Addition Test 3 (PASAT-3) Score at Month 36

    The Paced Auditory Serial Addition Test (PASAT) is a measure of cognitive function that specifically assesses auditory information processing speed and flexibility, as well as calculation ability. Score ranges from '0-60'. Higher scores reflect better neurological function and a positive change from baseline indicates improvement.

    Measured: Baseline (Day of Study 27025), Month 36

  7. Percentage of Relapse-Free Participants at Month 36

    A relapse was defined as the development of new or the exacerbation of existing neurological symptoms or signs, in the absence of fever, lasting for 24 hours and with a previous period for more than 30 days with a stable or an improving condition.

    Measured: Month 36

  8. Change From Baseline in Expanded Disability Status Scale (EDSS) Score at Month 36

    EDSS assesses disability in 8 functional systems. An overall score ranging from 0 (normal) to 10 (death due to MS) was calculated. The change in EDSS score at Month 36 was calculated as EDSS score at Month 36 minus EDSS score at baseline.

    Measured: Baseline (Day of Study 27025), Month 36

  9. Change From Baseline in Multiple Sclerosis Functional Composite (MSFC) Score at Month 36

    The MSFC is a multidimensional clinical outcome measure which consists of three sub-tests; Timed 25-Foot Walk, 9-Hole Peg Test and Paced Auditory Serial Addition Test-3(PASAT-3). The Timed 25-Foot Walk is a quantitative measure of lower extremity function. The 9-Hole Peg Test is a quantitative measure of upper extremity (arm and hand) function. The PASAT is a measure of cognitive function that specifically assesses auditory information processing speed and flexibility, as well as calculation ability. Standardized results (Z-scores) of these sub-tests and the overall MSFC Z-score as an average of these three Z-scores was calculated. Higher Z-scores reflect better neurological function and a positive change from baseline indicates improvement. An increase in score indicates an improvement (range -3 to +3).

    Measured: Baseline (Day 1 of Study 27025), Month 36

  10. Numbers of Participants With Binding Antibodies (BAb) and Neutralizing Antibody (NAb) at Month 36

    BAbs are all antibodies which are capable of binding to the investigational drug molecule (RNF) irrespective of their binding site. NAbs are defined as a subgroup of BAbs which bind to the active sites of the RNF and therefore neutralize its potency. NAbs were detected using a viral cytopathic assay. BAbs were measured by using an ELISA (Enzyme-linked immunosorbent assay).

    Measured: Month 36

  11. Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs) and AEs Leading to Treatment Discontinuation

    An AE was defined as any untoward medical occurrence in the form of signs, symptoms, abnormal laboratory findings, or diseases that emerges or worsens relative to baseline during a clinical study with an Investigational Medicinal Product (IMP), regardless of causal relationship and even if no IMP has been administered. SAE: Any AE that resulted in death; was life threatening; resulted in persistent/significant disability/incapacity; resulted in/prolonged an existing in-patient hospitalization; was a congenital anomaly/birth defect; or was a medically important condition.

    Measured: Month 24 up to Month 36 (DB treatment period for study 28981 (REFLEXION)

  12. Time to Conversion to Clinically Definite Multiple Sclerosis (CDMS) Defined by Either a Second Attack or a Sustained Increase (Greater Than or Equal to 1.5 Points) in the Expanded Disability Status Scale (EDSS) Score up to Month 60

    CDMS was defined by the occurrence of a second attack or relapse over 60 months in participants who presented with clinically isolated syndrome (CIS) accompanied by an abnormal magnetic resonance imaging (MRI) scan. EDSS assesses disability in 8 functional systems. An overall score ranging from 0 (normal) to 10 (death due to multiple sclerosis [MS]) was calculated. Time to conversion to CDMS was represented by Kaplan-Meier estimates of the cumulative percentage (%) of participants with CDMS.

    Measured: Baseline (Day 1 of Study 27025) up to 60 Months

  13. Time to Confirmed Expanded Disability Status Scale (EDSS) Progression up to 60 Months

    EDSS assesses disability in 8 functional systems. An overall score ranging from 0 (normal) to 10 (death due to MS) was calculated. A confirmed EDSS progression was defined EDSS greater than or equal to 1.0 point confirmed during a visit performed 6 months later. Time to confirmed EDSS progression was represented by Kaplan-Meier estimates of the cumulative percentage (%) of participants with confirmed EDSS progression.

    Measured: Baseline (Day 1 of Study 27025) up to 60 Months

  14. Number of Combined Unique Active (CUA) Lesions, New Time Constant 2 (T2) Lesions, New Gadolinium Enhanced (Gd+) Lesions and New T1 Lesions Per Participant Per Scan at Month 60

    Number of CUA lesions, new T2 lesions, new Gd+ Lesions and new T1 lesions were measured by using MRI scans.

    Measured: Month 60

  15. Change From Baseline in Time Constant 1 (T1) Hypointense Volume, and Time Constant 2 (T2) Lesion Volume at Month 60

    Change from baseline in lesion volume was measured by using MRI scans for T1 hypointense lesions and T2 lesions.

    Measured: Baseline (Day 1 of Study 27025), Month 60

  16. Percent Change From Baseline in Brain Volume at Month 60

    Percent Change in brain volume was measured by using MRI scans.

    Measured: Baseline (Day 1 of Study 27025), Month 60

  17. Percentage of Participants With Conversion to McDonald Multiple Sclerosis (MS) at Month 60

    The McDonald criteria use dissemination in time and space established by MRI findings to provide a clinical diagnosis for MS. Dissemination in time is established by a new T2 or Gd+ lesion found on a repeat MRI. Dissemination in space is established by the presence of any 3 of the following: 1 Gd+ lesion or 9 T2 bright lesions if there is no enhancement; greater than or equal to 1 infratentorial lesion; greater than or equal to 1 juxtacortical lesion; greater than or equal to 3 periventricular lesions.

    Measured: Month 60

  18. Change From Baseline in Paced Auditory Serial Addition Test 3 (PASAT-3) Score at Month 60

    The PASAT is a measure of cognitive function that specifically assesses auditory information processing speed and flexibility, as well as calculation ability. Score ranges from '0-60'. Higher scores reflect better neurological function and a positive change from baseline indicates improvement.

    Measured: Baseline (Day 1 of Study 27025), Month 60

  19. Percentage of Relapse-Free Participants at Month 60

    A relapse was defined as the development of new or the exacerbation of existing neurological symptoms or signs, in the absence of fever, lasting for 24 hours and with a previous period for more than 30 days with a stable or an improving condition.

    Measured: Month 60

  20. Change From Baseline in Expanded Disability Status Scale (EDSS) Score at Month 60

    EDSS assesses disability in 8 functional systems. An overall score ranging from 0 (normal) to 10 (death due to MS) was calculated. The change in EDSS score at Month 60 was calculated as EDSS score at Month 60 minus EDSS score at baseline.

    Measured: Baseline (Day 1 of Study 27025), Month 60

  21. Change From Baseline in Multiple Sclerosis Functional Composite (MSFC) Score at Month 60

    The MSFC is a multidimensional clinical outcome measure which consists of three sub-tests; Timed 25-Foot Walk, 9-Hole Peg Test and Paced Auditory Serial Addition Test-3(PASAT-3). The Timed 25-Foot Walk is a quantitative measure of lower extremity function. The 9-Hole Peg Test is a quantitative measure of upper extremity (arm and hand) function. The PASAT is a measure of cognitive function that specifically assesses auditory information processing speed and flexibility, as well as calculation ability. Standardized results (Z-scores) of these sub-tests and the overall MSFC Z-score as an average of these three Z-scores was calculated. Higher Z-scores reflect better neurological function and a positive change from baseline indicates improvement. An increase in score indicates an improvement (range -3 to +3).

    Measured: Baseline (Day 1 of Study 27025), Month 60

  22. Numbers of Participants With Binding Antibodies (BAb) and Neutralizing Antibody (NAb) at Month 60

    BAbs are all antibodies which are capable of binding to the RNF irrespective of their binding site. NAbs are defined as a subgroup of BAbs which bind to the active sites of the RNF and therefore neutralize its potency. NAbs were detected using a viral cytopathic assay. BAbs were measured by using an ELISA.

    Measured: Month 60

  23. Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs) and AEs Leading to Treatment Discontinuation

    An AE was defined as any untoward medical occurrence in the form of signs, symptoms, abnormal laboratory findings, or diseases that emerges or worsens relative to baseline during a clinical study with an Investigational Medicinal Product (IMP), regardless of causal relationship and even if no IMP has been administered. SAE: Any AE that resulted in death; was life threatening; resulted in persistent/significant disability/incapacity; resulted in/prolonged an existing in-patient hospitalization; was a congenital anomaly/birth defect; or was a medically important condition.

    Measured: Month 24 up to Month 60

Timeline

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

  1. First posted23 Dec 2008 (estimated)
  2. Study startDec 2008
  3. Primary completionAug 2011
  4. Study completionSep 2013

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
402 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00813709
Sponsor's protocol ID
28981
Acronym
REFLEXION
Status last verified
Jan 2017
First submitted
22 Dec 2008
Last updated
8 Mar 2017

Publications

  • Comi G, De Stefano N, Freedman MS, Barkhof F, Uitdehaag BM, de Vos M, Marhardt K, Chen L, Issard D, Kappos L. Subcutaneous interferon beta-1a in the treatment of clinically isolated syndromes: 3-year and 5-year results of the phase III dosing frequency-blind multicentre REFLEXION study. J Neurol Neurosurg Psychiatry. 2017 Apr;88(4):285-294. doi: 10.1136/jnnp-2016-314843. Epub 2016 Dec 30.

    PubMed 28039317

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing RNF in people with Multiple Sclerosis and Clinically Isolated Syndrome, run by Merck KGaA, Darmstadt, Germany at 57 sites in 24 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 16 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 8 Mar 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 57 sites in Russia, Bulgaria, Croatia, Poland, Romania and 19 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. 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 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

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 28 Oct 2013). 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?

Time to Conversion to Clinically Definite Multiple Sclerosis (CDMS) Defined by Either a Second Attack or a Sustained Increase (Greater Than or Equal to 1.5 Points) in the Expanded Disability Status Scale (EDSS) Score up to 36 Months (time frame: Baseline (Day 1 of Study 27025) up to 36 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 NCT00813709, 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 8 Mar 2017.

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