Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12613001027707
Ethics application status
Approved
Date submitted
11/09/2013
Date registered
16/09/2013
Date last updated
23/08/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
Alemtuzumab in Multiple Sclerosis Safety System development
Scientific title
Developing systems to minimise the risk of multiple sclerosis (MS) treatment with alemtuzumab
Secondary ID [1] 283202 0
Nil
Universal Trial Number (UTN)
U1111-1147-9190
Trial acronym
AMS3
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Multiple Sclerosis 290062 0
Condition category
Condition code
Neurological 290439 290439 0 0
Multiple sclerosis

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
2
Target follow-up type
Years
Description of intervention(s) / exposure
A two year observational study of open label treatment with alemtuzumab for multiple sclerosis (MS). The aim of the study is to develop efficient information-technology (IT) based methods for the monthly monitoring required by the risk management protocols after treatment with alemtuzumab. The effectiveness of alemtuzumab in MS has already been demonstrated in randomised trials and is not the subject of this study.

Normally after treatment of MS with alemtuzumab patients are required to have ongoing monthly pathology monitoring. The study is to test the successful development of an electronic semi-automated monitoring of pathology results. There is no additional involvement for participants other than the normal monthly pathology testing per alemtuzumab treatment protocol.
Intervention code [1] 287926 0
Not applicable
Comparator / control treatment
Open label treatment with alemtuzumab per CAREMS1 protocol, no control group.
Control group
Uncontrolled

Outcomes
Primary outcome [1] 290465 0
Successful development of an IT architecture to monitor monthly pathology results electronically after treatment of MS patients with alemtuzumab.

The success will be measured by whether the package works, including integration between pathology company results and our fetching programme and interrogation of the data remotely and generation of remote alerts.
Timepoint [1] 290465 0
One year from commencement
Secondary outcome [1] 304561 0
The secondary endpoints are to measure the role of the pre treatment safety screen and to measure the functional capacity of PRIME.

Treatment and safety data will be collected but are not endpoints of this study.

Time and cost for alemtuzumab risk management protocol (RMP) vs immunosuppressionscreen (data progressively accrued, available at time of last patient enrolled). Measure = cost per patient for RMP vs immunosuppression screen.

Timepoint [1] 304561 0
Two years from commencement
Secondary outcome [2] 304615 0
Additional risks identified with immunosuppression screen (data progressively accrued, available at time of last patient enrolled). Measure = elaborate on specific risks
Timepoint [2] 304615 0
Two years
Secondary outcome [3] 304616 0
Centralise all appropriately coded alemtuzumab study results in a single web browser (Webster). Measure = yes / no
Timepoint [3] 304616 0
Two years
Secondary outcome [4] 304617 0
Development of a functioning automated system. Measure = yes / no

Timepoint [4] 304617 0
Two years
Secondary outcome [5] 304618 0
Testing of a system with dummy results. Measure = yes / no
Timepoint [5] 304618 0
Two years
Secondary outcome [6] 304619 0
Testing of a system with real world results from patients anywhere in the state of NSW, Australia. Measure = yes / no
Timepoint [6] 304619 0
Two years
Secondary outcome [7] 304620 0
Monitoring of tests: 95% of results reviewed by automated system once operational to end 24 months. Measure = yes / no
Timepoint [7] 304620 0
Two years
Secondary outcome [8] 304621 0
Flags for deviation from results window or results parameters - 95% generated by automated system once operational to end June 2014. Measure = yes / no
Timepoint [8] 304621 0
Two years
Secondary outcome [9] 304622 0
Human factors integration: were there results or lack thereof that could not be finalized within 7 calendar days due to human factors (i.e. nurse not acting on results, inability to communicate with doctor or patient; patient not complying with need for test etc). Measure = yes / no
Timepoint [9] 304622 0
Two years

Eligibility
Key inclusion criteria
1. Willing to provide informed consent to both treatment with alemtuzumab and inclusion in the PRIME clinical decision support system monitoring procedures
2. Age 18 or older as of the date the consent is signed
3. Definite relapsing remitting MS by McDonald 2010 criteria
4. Cranial MRI scan demonstrating white matter lesions attributable to MS within 1 year of Screening
5. Active MS as signified by at least 2 relapses in the last 2 years and at least 1 relapse in the last 1 year
6. Either:
a. Failure of first line disease-modifying treatment as determined by: at least 1 relapse of MS despite treatment with a TGA-approved treatment for MS (interferons, glatiramer, teriflunomide, fingolimod or natalizumab), or at least 1 relapse in a patient unable to be treated with TGA-approved MS treatments due to intolerance or unacceptable risks of these treatments
b. Previously untreated MS that is associated with at least one gadolinium enhancing lesion on MRI in the last 1 year.
7. Diagnosed disease duration <= 10years
8. Baseline EDSS 0 – 4.0
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
a. As per CAMMS03409 amendment 2:
i. Does not wish to receive alemtuzumab
ii. Ongoing participation in any other investigational study
iii. Has received alemtuzumab off-label
iv. Known bleeding disorder (eg, dysfibrinogenemia, factor IX deficiency, hemophilia, Von Willebrand's disease, Disseminated Intravascular Coagulation [DIC], fibrinogen deficiency, or other clotting factor deficiency) or therapeutic anticoagulation
v. Diagnosis of immune thrombocytopenic purpura (ITP), or other autoimmune hematologic abnormality.
vi. History of malignancy, except basal cell skin carcinoma
vii. Intolerance of pulsed corticosteroids, especially a history of steroid psychosis
viii. Significant non-MS autoimmune disease including but not limited to: immune cytopenias, rheumatoid arthritis, systemic lupus erythematosus, other connective tissue disorders, vasculitis, inflammatory bowel disease, severe psoriasis, or anti-glomerular basement membrane disease (anti-GBM disease, also known as Goodpasture’s disease)
ix. Major psychiatric disorder or epileptic seizures not adequately controlled by treatment
x. Known infection with hepatitis B or C virus, seropositivity for human immunodeficiency virus (HIV).
xi. History of invasive fungal infections
xii. Unwilling to agree to use a reliable and acceptable contraceptive method for at least 6 months following each alemtuzumab treatment cycle (fertile patients only). Reliable and effective contraceptive method(s) include: intrauterine device (IUD), hormonal-based contraception, surgical sterilization, abstinence or double-barrier contraception (condom and occlusive cap [diaphragm or cervical cap with spermicide])
b. Plus (local exclusion criteria)
i. Not resident in NSW
ii. Not able to access Douglass Hanly Moir pathology services
iii. Not able or likely to fulfil the requirements of the study for any other reason
iv. Not able to access electronic reminders and alerts (patient must have both a mobile (cell) phone and a valid regularly checked email address, the patient’s designate person must have at least one of these two methods of contact, prefer both)
v. Allergic or intolerant of any agent required for the completion of this study (i.e alemtuzumab, gadolinium contrast)
vi. No history of primary infection or vaccination with varicella zoster virus, until vaccinated
vii. Other significant active or latent infection until treated
viii. Any other reason that an investigator regards as a contraindication to entering or ability to complete the study
c. The following are not exclusion criteria but caution should be exercised in including patients with these criteria noting that these were exclusion criteria for the alemtuzumab RCTs
i. Prior exposure to natalizumab, fingolimod, mitoxantrone, azathioprine, cladribine, cyclophosphamide, cyclosporine A, methotrexate, or any other immunosuppressive agent
ii. Patients > 50 years of age
iii. Disease duration 5-10 years after diagnosis
iv. EDSS 3.5-4
v. Patients with known thyroid autoimmunity or thyroid antibodies. Such patients are highly likely to develop clinical thyroid autoimmunity and this should be discussed with the patient.

Study design
Purpose
Screening
Duration
Longitudinal
Selection
Defined population
Timing
Prospective
Statistical methods / analysis
Statistical methods

As this is a development study rather than a drug trial there are no complex statistical requirements arising and no planned analyses other than simple summary statistics for performance of PRIME.

Where required the statistical assistance of the Concord hospital liaison statistician shall be used, using SPSS or graphpad as appropriate.

Summary statistics will be computed and displayed by treatment group and scheduled assessment time. Summary statistics for continuous variables will minimally include n, mean, standard deviation, minimum, median, and maximum. For categorical variables, frequencies and percentages will be presented. Graphical displays will be provided as appropriate.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
2/12/2013
Actual
9/04/2014
Date of last participant enrolment
Anticipated
Actual
30/10/2014
Date of last data collection
Anticipated
Actual
31/10/2016
Sample size
Target
10
Accrual to date
Final
10
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 1506 0
Concord Repatriation Hospital - Concord
Recruitment postcode(s) [1] 7346 0
2139 - Concord Repatriation Hospital

Funding & Sponsors
Funding source category [1] 287944 0
Commercial sector/Industry
Name [1] 287944 0
Genzyme Sanofi
Country [1] 287944 0
Australia
Primary sponsor type
Hospital
Name
Sydney Local Health District
Address
1 Hospital Rd
Concord Hospital
NSW 2139
Country
Australia
Secondary sponsor category [1] 286662 0
None
Name [1] 286662 0
Address [1] 286662 0
Country [1] 286662 0
Other collaborator category [1] 277612 0
Commercial sector/Industry
Name [1] 277612 0
Medical Safety Systems
Address [1] 277612 0
4/94 Mallett St
Camperdown NSW 2050
Country [1] 277612 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 289872 0
Concord Repatriation General Hospital
Ethics committee address [1] 289872 0
Ethics committee country [1] 289872 0
Australia
Date submitted for ethics approval [1] 289872 0
01/10/2013
Approval date [1] 289872 0
24/01/2014
Ethics approval number [1] 289872 0
HREC/13/CRGH/256 CH62/6/2013- 180 – S Reddel Alemtuzumab Medical Safety Systems Study (AMS3) Developing systems to minimise the risk of MS treatment with alemtuzumab

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes
Attachments [1] 3020 3020 0 0
/AnzctrAttachments/364953-AMS3 poster monitoring v2.pdf (Publication)
Attachments [2] 3021 3021 0 0
/AnzctrAttachments/364953-AMS3 poster clinical.pdf (Publication)

Contacts
Principal investigator
Name 42870 0
A/Prof Stephen Reddel
Address 42870 0
Level 5W
1 Hospital Rd
Concord Hospital
NSW 2139`
Country 42870 0
Australia
Phone 42870 0
+612 97676129
Fax 42870 0
Email 42870 0
[email protected]
Contact person for public queries
Name 42871 0
Rene Yon
Address 42871 0
Medical Safety Systems
4/94 Mallett St
Camperdown NSW 2050
Country 42871 0
Australia
Phone 42871 0
+612-93510730
Fax 42871 0
Email 42871 0
[email protected]
Contact person for scientific queries
Name 42872 0
Stephen Reddel
Address 42872 0
Level 5W
1 Hospital Rd
Concord Hospital
NSW 2139`
Country 42872 0
Australia
Phone 42872 0
+612 97676129
Fax 42872 0
Email 42872 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseSuccessful implementation of an automated electronic support system for patient safety monitoring: The alemtuzumab in multiple sclerosis safety systems (AMS3) study.2019https://dx.doi.org/10.1177/1352458518783673
N.B. These documents automatically identified may not have been verified by the study sponsor.