Safety, Tolerability, and Activity Study of ISIS SOD1Rx to Treat Familial Amyotrophic Lateral Sclerosis (ALS) Caused by SOD1 Gene Mutations

Familial Amyotrophic Lateral Sclerosis Clinical Trial

— SOD-1  

Official title:

A Phase 1, Double-Blind, Placebo-Controlled, Dose-Escalation Study of the Safety, Tolerability, and Pharmacokinetics of ISIS 333611 Administered Intrathecally to Patients With Familial Amyotrophic Lateral Sclerosis Due to Superoxide Dismutase 1 Gene Mutations

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01041222
• Other study ID #: ISIS 333611- CS1
• Status: Completed
• Phase: Phase 1
• First received: December 30, 2009
• Last updated: April 12, 2012
• Start date: January 2010
• Est. completion date: January 2012

Study information

• Verified date: April 2012
• Source: Ionis Pharmaceuticals, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This study will test the safety, tolerability and pharmacokinetics of single doses of ISIS 333611 administered into the spinal canal as 12 hour infusions.

Description:

This study will test the safety, tolerability, and pharmacokinetics of single doses of ISIS 333611 administered as 12-hour intrathecal infusions. Four dose levels (0.15, 0.5, 1.5 and 3 mg) will be evaluated sequentially. The volume of the infusion is 0.25 mL/12 hours. Each dose level will be studied in a cohort of 8 patients where 6 are randomized to active treatment with ISIS 333611 and 2 are randomized to placebo.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 33
• Est. completion date: January 2012
• Est. primary completion date: December 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Clinical signs of weakness attributed to ALS.

• Familial ALS with a documented SOD1 gene mutation.

• Age 18 years or older.

• Capable of providing informed consent and willing to comply with trial procedures and time commitments.

• Vital capacity (VC) at least 50% predicted value for gender, height and age at screening and not using invasive respiratory support.

• If taking riluzole, patients must be on stable dosage for at least 30 days prior to starting the study and expect to remain at that dosage until the end of the study.

• Medically able to undergo temporary insertion of intrathecal catheter.

• Normal test results for coagulation parameters.

Exclusion Criteria:

• Treatment with another investigational drug for ALS (e.g. pyrimethamine, ceftriaxone, lithium, tamoxifen, arimoclomol, high dose creatine, biological agent, or device within 1-month of Screening or 5 half-lives of study agent, whichever is longer. No prior treatment with siRNA, cell transplant, or gene therapy is allowed.

• Dosing in ISIS 333611-CS1 in a previous dose cohort within 60 days of screening.

• Presence of any of the following clinical conditions:

1. Drug abuse or alcoholism within one year of the Screening visit.

2. Unstable cardiac, pulmonary, renal, hepatic, endocrine, hematologic function, or active infectious disease.

3. Documented history of HIV infection.

4. Unstable psychiatric illness defined as psychosis or untreated major depression within 90 days of the Screening Visit.

• Any condition that may impact intrathecal infusion including:

1. History of structural spinal disease including tumors and hyperplasia.

2. Presence of an implanted shunt for the drainage of CSF or an implanted CNS catheter.

3. Clinically significant abnormalities in hematology or clinical chemistry parameters as assessed by the Site Investigator during the Screening visit.

4. Ongoing medical condition that according to the Site Investigator would interfere with the conduct and assessments of the study. Examples are medical disability (e.g., severe degenerative arthritis, compromised nutritional state, peripheral neuropathy) that would interfere with the assessment of safety and efficacy of study material or device performance, or would compromise the ability of the patient to undergo study procedures.

5. ALT or AST >/= 3 x ULN, unless discussed with and approved by the Medical Monitor.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Amyotrophic Lateral Sclerosis
• Familial Amyotrophic Lateral Sclerosis
• Motor Neuron Disease
• Sclerosis

Intervention

Drug:
• ISIS 333611
5 arms of 12 hour infusion: Arm 1 0.15 mg, Arm 2 0.5 mg, Arm 3 1.5 mg, Arm 4 3.0 mg, matching volume of placebo

Locations

Country	Name	City	State
United States	Johns Hopkins University	Baltimore	Maryland
United States	Massachusetts General Hospital-East, Neurology Clinical Trials Unit	Charlestown	Massachusetts
United States	Methodist Neurological Institute	Houston	Texas
United States	Washington University School of Medicine	St. Louis	Missouri

Sponsors (3)

Lead Sponsor	Collaborator
Ionis Pharmaceuticals, Inc.	ALS Association, Muscular Dystrophy Association

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To evaluate the safety, tolerability, and pharmacokinetics of four dose levels of ISIS 333611		Safety analysis for dose escalation after Study Day 8	Yes