Combination Therapy With Dalfampridine and Locomotor Training for Chronic, Motor Incomplete Spinal Cord Injury

Kessler Foundation

Status and phase: Completed; Phase 2

Conditions: Spinal Cord Injury

Treatments: Drug: Placebo; Drug: Dalfampridine

Study type: Interventional

Funder types: Other; Other U.S. Federal agency; Industry

Identifiers

NCT01621113

D-732-12

H133N110020 (Other Grant/Funding Number)

Details and patient eligibility

About

The purpose of this study is to determine the efficacy, safety, and tolerability of treatment with dalfampridine in combination with locomotor training in persons with chronic, motor incomplete SCI.

Full description

Research suggests that combining therapies could result in important gains in restoring function and improving quality of life in persons with spinal cord injury (SCI). Locomotor training is an activity-dependent rehabilitation therapy that provides repetitive stepping facilitated by manual assistance and body weight support on a treadmill. Recent studies report improvements in walking and standing in individuals with motor incomplete SCI that have undergone intensive standardized locomotor training therapy. Extended release dalfampridine (also known as fampridine or 4-aminopyridine [4-AP]) is a broad spectrum potassium channel blocker that has been shown in animal studies to increase conduction of action potentials in demyelinated axons. Dalfampridine was recently approved by the U.S. Food and Drug Administration (FDA) as a treatment to improve walking in persons with multiple sclerosis (MS). Demyelination is also a prominent feature of incomplete SCI that contributes to the clinical presentation of persons with these injuries.

The purpose of this study is to determine the efficacy, safety, and tolerability of treatment with dalfampridine in combination with locomotor training in persons with chronic, motor incomplete SCI. We hypothesize that persons undergoing combination therapy with dalfampridine and locomotor training will show significantly greater improvements in walking speed and other measures of SCI function than those receiving locomotor training alone.

Enrollment: 27 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 18 to 70 years, inclusive;
• Neurological impairment secondary to a traumatic spinal cord injury that occurred at least twelve (12) months prior to the screening visit;
• Neurological level of the injury between C4 and T10, inclusive;
• The injury is classified as motor incomplete (AIS grade C or D);
• Able and willing to comply with the study protocol, including availability for all scheduled clinic visits and locomotor training sessions.

Exclusion criteria

• The participant is a lactating female, or a female of childbearing potential who is sexually active, has not had a hysterectomy or oophorectomy, and is not using an approved birth control method (e.g. tubal ligation, implantable contraception device, oral or injectable contraceptive, barrier method, or sexual activity restricted to vasectomized partner);
• The participant has a history of seizures or treatment for seizure disorders;
• The participant has renal impairment (Creatinine Clearance < 80 mL/min);
• The participant has a known allergy to pyridine-containing substances or any of the inactive ingredients of the dalfampridine;
• The participant has a clinically significant abnormal laboratory values or an abnormal electrocardiogram (ECG);
• The participant has evidence of significant, diffuse, or generalized lower motor neuron damage;
• The participant has received new concomitant medication less than 3 weeks before the study or has a dose of current concomitant medication that is expected to change during study;
• The participant has received botulinum toxin injection for spasticity within 4 months of the screening visit;
• The participant has taken any other investigational drugs within 30 days before screening;
• The participant is known to have been treated previously with dalfampridine (4 aminopyridine) in any formulation, whether through participation in a previous fampridine study or by self-medication.
• The participant has received locomotor training therapy within 6 months of the screening visit;
• The participant has a history of alcohol or drug abuse in the previous year;
• The participant has a medical condition that would interfere with interpretation of study results or study conduct.

Note: Due to equipment and safety issues associated with locomotor training, participants must weigh less than 300 lbs.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

---

27 participants in 2 patient groups, including a placebo group

Locomotor Training + Dalfampridine

Experimental group

Description:

Subjects randomized to this group will undergo 10 weeks of double-blind treatment with extended release dalfampridine tablets (10 mg twice daily) while simultaneously receiving locomotor training therapy (5 sessions per week x 10 weeks = 50 sessions total).

Treatment:

Drug: Dalfampridine

Locomotor Training + Placebo

Placebo Comparator group

Description:

Subjects randomized to this group will undergo identical treatment, but will take placebo tablets while simultaneously receiving locomotor training therapy (5 sessions per week x 10 weeks = 50 sessions total).

Treatment:

Drug: Placebo