Rebif New Formulation (RNF) Quality of Life (QOL) Study - Study Results

Rebif New Formulation (RNF) Quality of Life (QOL) Study (RebiQoL)

This study is ongoing, but not recruiting participants.

Study NCT00472797 Information provided by EMD Serono

First Received: May 10, 2007 Last Updated: September 9, 2009 History of Changes

Study Type:	Interventional
Study Design:	Randomized, Open Label, Uncontrolled, Parallel Assignment
Condition:	Relapsing Multiple Sclerosis
Interventions:	Drug: Rebif New Formulation Non Titrated Drug: Rebif New Formulation Titrated

Participant Flow

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Recruitment Details

Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
232 subjects were recruited from 25 Multiple Sclerosis (MS) Clinics in the US from April 2007 through November 2007.

Pre-Assignment Details

Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
Run-in period (up to 30 days) on Rebif® 44 mcg tiw: The run-in period included a Screening Visit; assessments consisted of informed consent, medical/disease history, physical exam and laboratory assessments which were performed in the two-week period prior to Study Day 1, (prior to the first dose of Rebif New Formulation (RNF).

Reporting Groups

	Description
Rebif New Formulation (RNF) Non-Titrated	Rebif New Formulation Non-Titrated
Rebif New Formulation (RNF) - Titrated	Rebif New Formulation - Titrated

Participant Flow: Overall Study

	Rebif New Formulation (RNF) Non-Titrated	Rebif New Formulation (RNF) - Titrated
STARTED	119	113
COMPLETED	115	112
NOT COMPLETED	4	1

Baseline Characteristics

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Reporting Groups

	Description
Rebif New Formulation (RNF) - Non-Titrated	No text entered.
Rebif New Formulation (RNF) - Titrated	No text entered.

Baseline Measures

	Rebif New Formulation (RNF) - Non-Titrated	Rebif New Formulation (RNF) - Titrated	Total
Number of Participants [units: participants]	119	113	232
Age [units: participants]
<=18 years	0	0	0
Between 18 and 65 years	119	113	232
>=65 years	0	0	0
Age [units: years] Mean ± Standard Deviation	44.6 ± 9.0	42.8 ± 9.4	43.7 ± 9.2
Gender [units: participants]
Female	91	89	180
Male	28	24	52
Region of Enrollment [units: participants]
United States	119	113	232

Outcome Measures

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1. Primary:

Percent Change in Global Side Effects (GSE) on Multiple Sclerosis Treatment Concerns Quesionnaire (MSTCQ) [ % change from Baseline to Week 12 ]

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2. Secondary:

Total Score for Global Side Effects on Multiple Sclerosis Treatment Concerns Questionnaire (MSTCQ) [ Baseline and Week 12 ]

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3. Secondary:

Change in Score From Baseline to Week 12 for All Domains Other Than Global Side Effects on Multiple Sclerosis Treatment Concerns Questionnaire (MSTCQ) [ Baseline to Week 12 ]

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4. Secondary:

Total Score on Short-Form McGill Pain Questionnaire (SF-MPQ): Change in Baseline to Wk 12 [ Baseline to Week 12 ]

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5. Secondary:

Tolerability in Pain Using Visual Analog Scale (VAS) [ Baseline to Week 12 ]

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Measure Type	Secondary
Measure Title	Tolerability in Pain Using Visual Analog Scale (VAS)
Measure Description	The SF-MPQ included a visual analog scale, ranging from 0 to 100 mm, on which subjects rate pain from no pain (0 mm) to worst possible pain (100 mm). A rating of <5 mm was considered pain-free.
Time Frame	Baseline to Week 12
Safety Issue	No

Population Description

Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
ITT

Reporting Groups

	Description
Rebif New Formulation (RNF) Non-Titrated	Rebif New Formulation Non-Titrated
Rebif New Formulation (RNF) - Titrated	Rebif New Formulation - Titrated
All Rebif New Formulation (RNF) Subjects	All subjects combined in Intent to Treat (ITT) Population

Measured Values

	Rebif New Formulation (RNF) Non-Titrated	Rebif New Formulation (RNF) - Titrated	All Rebif New Formulation (RNF) Subjects
Number of Participants Analyzed [units: participants]	119	113	232
Tolerability in Pain Using Visual Analog Scale (VAS) [units: Participants]
Baseline - No. of Subjects Pain Free	52	48	100
Week 12 - No. of Subjects Pain Free	53	48	101

No statistical analysis provided for Tolerability in Pain Using Visual Analog Scale (VAS)

6. Secondary:

Tolerability - Redness at Injection Site [ Baseline to Week 12 (LOCF) ]

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Serious Adverse Events

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Other Adverse Events

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More Information

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Certain Agreements:

Principal Investigators are NOT employed by the organization sponsoring the study.

There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

The agreement is:

	The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
	The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
	Other disclosure agreement that restricts the right of the PI to discuss or publish trial results after the trial is completed. Restriction Description: Neither Institution nor any Principal Investigators shall publish or present any results from such Study to any third parties until: (i) EMD Serono publishes the results from all sites participating in such Study; (ii) Institution receives notification from EMD Serono that publication of the multi-site results is no longer planned; or (iii) twenty-four (24) months following the completion of the multi-site study at all sites, whichever occurs first.

Limitations and Caveats

Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
No text entered.

Results Point of Contact:

Name/Title: Fernando Dangond, MD
Organization: EMD Serono, INc.
phone: 781 681 2348
e-mail: fernando.dangond@emdserono.com

No publications provided

Responsible Party:	EMD Serono, Inc ( Ahmad Al-Sabbagh, Vice President Medical Affairs, US Neurology )
Study ID Numbers:	27955
Study First Received:	May 10, 2007
Results First Received:	February 18, 2009
Last Updated:	September 9, 2009
ClinicalTrials.gov Identifier:	NCT00472797 History of Changes
Health Authority:	United States: Food and Drug Administration