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

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

This study has been completed.

Study NCT00472797 Information provided by EMD Serono

First Received on May 10, 2007. Last Updated on August 17, 2010 History of Changes

Results First Received: February 18, 2009

Study Type:	Interventional
Study Design:	Allocation: Randomized; Endpoint Classification: Safety Study; Intervention Model: Parallel Assignment; Masking: Open Label; Primary Purpose: Supportive Care
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 a new formulation of rebif)

Reporting Groups

	Description
New Formulation of Rebif - Non-Titrated	The new formulation of rebif is not approved and under investigation in the US
New Formulation of Rebif - Titrated	The new frmulation of rebif is not approved and under investigation in the US

Participant Flow: Overall Study

	New Formulation of Rebif - Non-Titrated	New Formulation of Rebif - Titrated
STARTED	119	113
COMPLETED	115	112
NOT COMPLETED	4	1

Baseline Characteristics

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Reporting Groups

	Description
New Formulation of Rebif - Non-Titrated	No text entered.
New Formulation of Rebif - Titrated	No text entered.

Baseline Measures

	New Formulation of Rebif - Non-Titrated	New Formulation of Rebif - 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) [ Time Frame: % 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) [ Time Frame: 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) [ Time Frame: 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 [ Time Frame: Baseline to Week 12 ]

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5. Secondary:

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

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6. Secondary:

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

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7. Other Pre-specified:

SF-36 Physical and Mental Component Scores [ Time Frame: Change from Baseline to Each Visit ]

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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:	Ahmad Al-Sabbagh, Vice President Medical Affairs, US Neurology, EMD Serono, Inc
ClinicalTrials.gov Identifier:	NCT00472797 History of Changes
Other Study ID Numbers:	27955
Study First Received:	May 10, 2007
Results First Received:	February 18, 2009
Last Updated:	August 17, 2010
Health Authority:	United States: Food and Drug Administration