Combination Therapy (Provigil + Avonex) to Treat Cognitive Problems in MS

Relapsing-Remitting Multiple Sclerosis Clinical Trial

Official title:

Combination Therapy (Provigil + Avonex) in the Treatment of Attention Problems in Patients With Relapsing-Remitting MS

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00210301
• Other study ID #: 001
• Status: Recruiting
• Phase: N/A
• First received: September 13, 2005
• Last updated: September 6, 2006
• Start date: January 2003

Study information

• Verified date: August 2005
• Source: Institute for Clinical Research
• Contact: Jeffrey A Wilken, Ph.D.
• Phone: 202-745-8000
• Email: jeffrey.wilken[@]med.va.gov
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

MS has been associated with fatigue, attention problems, and a number of cognitive difficulties. There is no treatment approved yet to treat these problems. We hypothesize that the addition of Provigil to an existing immunomodulatory agent (Avonex) will lead to improved fatigue, attention, and overall cognition in MS patients with attention problems.

Description:

MS has been associated with fatigue, attention problems, and a number of cognitive difficulties. There is no treatment approved yet to treat these problems. Although certain immunomodulatory treatments may slow the progression of cogntiive difficulties, they are not therapy for the progression of or new onset of such problems. Therefore, in order to treat such problems, it is likely that adjunctive medications focused on fatigue and cognition are needed. We hypothesize that the addition of Provigil to an existing immunomodulatory agent (Avonex) will lead to improved fatigue, attention, and overall cognition in MS patients with attention problems.

Study Period: 6 to 12-month competitive enrollment period, two groups (Avonex and Avonex +Provigil 200 mg QD ) undergo baseline (prior to starting Provigil), 2-month, and 4-month neuropsychological evaluations. Total length of study, once initiated, (including 2 month preparation period, 6 to 12-month competitive enrollment period through final four-month visit) is 12 to 18 months.

Primary Objective: To investigate whether Provigil in combination with Avonex is safe, and tolerable in patients with RRMS.

Secondary Objectives:

1. To determine whether Provigil (modafinil) in combination with Avonex(interferon β-1a) is useful in treating deficits in attention, as measured by objective neuropsychological tests, in patients with RR-MS

2. To determine whether combination therapy (Avonex +Provigil) favorably impacts other domains of cognition that are reliant on attention (e.g., memory, psychomotor functioning), as measured by objective neuropsychological tests, in patients with RR-MS

3. To determine whether improvement in fatigue (related to treatment) predicts improvements in attention and cognitive performance in MS patients

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years to 65 Years

Eligibility

Inclusion Criteria:

• Patients entering the study will:

• Be taking Avonex

• Have normal laboratory blood tests and EKG

• Be complaining of attention problems to treating neurologist

• Be English-speaking males and females between the ages of 25 and 60, inclusive [If patient is female, she must

• Be surgically sterile; or

• Be 2 years postmenopausal; or

• If of child-bearing potential, must be using a medically accepted method of birth control and agree to continue to use this method for the duration of the study (i.e., barrier method with spermicide, steroidal contraceptive [oral, implanted, and Depo-Provera contraceptives must be used in conjunction with a barrier method], IUD, or abstinence)]

• Have clinically definite RR MS with disease duration of less than 10 years

• Have an EDSS score between 0 and 5.5

• Have corrected vision of no worse than 20/50

• Have between 10 and 20 years of education

• Be cerebral-stimulant free for at least one week prior to Attention Screening

• Be able to complete self-rating scales and cognitive assessment tools

• Have provided written informed consent

• To have performed at least one standard deviation below normative expectation on at least two of four measures in the attention screening evaluation

Exclusion Criteria:

• Patients entering the study will NOT:

• A history of heart disease or liver dysfunction

• Have abnormal EKG or laboratory blood work,

• Have a history of psychosis

• Be a significant risk of suicide

• Be abusing alcohol (current and within last 2 years)

• Be abusing controlled substances (current and within last 2 years)

• Have any medical ailment which can produce fatigue, such as lupus, anemia or thyroid disease

• Have any history of clinical deviation from normal ranges in the physical examination

• Have an unstable medical disorder, or medical contraindication to the use of Provigil

• Have any history of head injury, seizures, or neurological conditions involving the central nervous system other than RR MS

• Have any disorder that may interfere with drug absorption, distribution, metabolism, or excretion, including gastrointestinal surgery

• Be a pregnant or lactating female (any patient becoming pregnant during the study will be discontinued)

• Have received any investigational product within 30 days of Cognitive Screening

• Have upper extremity dysfunction that prohibits them from using a computer mouse writing with a pencil

• Be colorblind

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Multiple Sclerosis
• Multiple Sclerosis, Relapsing-Remitting
• Relapsing-Remitting Multiple Sclerosis

Intervention

Drug:
• Provigil (modafinil)

Locations

Country	Name	City	State
United States	Veterans Affairs Medical Center	Washington	District of Columbia

Sponsors (1)

Lead Sponsor	Collaborator
Institute for Clinical Research

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Comparison of AE's and SAE's to determine safety of combination
Secondary	Full neuropsychological test battery (including fatigue measures) to assess effect on fatigue and cognition.