Clinical Trial of Sodium Phenylbutyrate in Children With Spinal Muscular Atrophy Type I

Spinal Muscular Atrophy Type I Clinical Trial

— NPTUNE 02  

Official title:

Phase I/IIa Clinical Trial of Sodium Phenylbutyrate in Pediatric Subjects With Type I Spinal Muscular Atrophy

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00439218
• Other study ID #: N01NS42361_NPTUNE02
• Secondary ID: HHSN265200423611
• Status: Terminated
• Phase: Phase 1/Phase 2
• First received: February 22, 2007
• Last updated: October 27, 2010
• Start date: January 2008
• Est. completion date: May 2009

Study information

• Verified date: May 2009
• Source: Westat
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to identify the maximum tolerated dosage of sodium phenylbutyrate in children with spinal muscular atrophy type I; and to determine if the drug has an effect on SMN mRNA and protein levels.

Description:

Spinal muscular atrophy (SMA) is a genetic, neuromuscular disorder caused by progressive degeneration of motor neurons in the spinal cord, which results from the loss of survival motor neuron (SMN) protein. The disorder is characterized by weakness and wasting of the voluntary muscles and is a leading cause of hereditary infant death. Sodium phenylbutyrate—a drug used to treat urea cycle disorders—may increase the amount of SMN protein in the body and consequently may decrease the severity of SMA. However, this has not yet been proven.

In this multicenter trial, physicians will evaluate multiple dosage levels of sodium phenylbutyrate to determine the maximum tolerated dose (MTD), or the highest dose that can be safely given to children with SMA type I. The initial dosage tested will be 500 mg/kg/day. Depending upon tolerability, subsequent groups may receive dosages of 675, 900, or 1200 mg/kg/day. Blood levels of SMN mRNA and protein will also be measured to determine whether sodium phenylbutyrate can increase the amount of these two biomarkers in the blood. Up to 24 children will be enrolled in the study, and will be on sodium phenylbutyrate for 12 weeks. The MTD will be determined based on safety data from Day 0 through the Day 29 visit. Participants will continue to be monitored for safety and SMN mRNA and protein levels through the 12 week study drug administration period.

Potential participants will be screened by having their complete medical and treatment histories recorded, as well as undergoing a physical examination, laboratory tests, and an electrocardiogram (EKG). Parents of eligible participants will receive a supply of sodium phenylbutyrate and instructions on how to administer the drug. Participants will return to the clinic on days 8, 22, 29, and at weeks 8 and 12 of the study to update their medical and treatment histories, have a physical exam, and have blood and urine collected for laboratory testing. A follow-up clinic visit will occur approximately 14 days after the last dose of sodium phenylbutyrate is given. During this visit participants will update their complete medical and treatment histories and have a physical examination. Duration of the study is about 14 weeks.

Information from this study, which is part of the NINDS Pilot Therapeutics Network (NPTUNE), may be used for future studies to determine if sodium phenylbutyrate is effective for treating SMA, and if the drug has an effect on SMA symptoms.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 5
• Est. completion date: May 2009
• Est. primary completion date: May 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 2 Months to 48 Months

Eligibility

Inclusion Criteria:

Subjects must meet all of the following inclusion criteria within 14 days prior to receiving the first dose of study drug.

• Weakness and hypotonia consistent with a clinical diagnosis of spinal muscular atrophy (SMA) type I

• Laboratory documentation of homozygous absence of SMN1 exon 7

• Older than two months of age, but younger than 48 months of age, at the time of enrollment. If the subject is older than 24 months of age at the time of enrollment, the subject must require ventilatory support for at least 6 hours/day.

• Written informed consent of parents/guardian

• Weight greater than or equal to 7 kilograms

• Laboratory results drawn within 14 days prior to start of study drug demonstrating:

Hemoglobin within normal range at the clinical site; White Blood Cell Count = 3000/mm³; Platelet Count = 75,000/mm³; Lipase and Amylase = 1.5 x upper limit of normal (ULN) in the absence of associated clinical symptoms; AST and ALT =2.5x ULN; Bilirubin = 1.5x ULN in the absence of associated clinical symptoms; Sodium = 130 and = 150 mmol/L; Potassium =3.0 and = 5.5 mmol/L; Chloride = 110 mmol/L; Calcium = 8.0 mg/dL; Bicarbonate = 16 mmol/L; Glucose = 55 and = 160 mg/dL; BUN = 39 mg/dL; Creatinine = 1.5 x ULN

• Subjects who are on ventilators may enroll in the protocol providing they have been on stable ventilator settings for at least the prior two weeks.

• Subject is expected to survive for at least 6 months following study entry

Exclusion Criteria:

Subjects who meet any of the following criteria will be excluded from participating in the study:

• Evidence of renal dysfunction, blood dyscrasia, hepatic insufficiency, symptomatic pancreatitis, cardiac arrhythmia, congenital heart defect, known history of metabolic acidosis, hypertension, significant central nervous system impairment, or neurodegenerative or neuromuscular disease other than SMA.

• Any adverse event = Grade 3 at the time of screening based on the protocol toxicity grading table

• Any acute co-morbid condition interfering with the well-being of the subject within 7 days of enrollment including bacterial infection, viral infectious process, food poisoning, temperature > 99.0ºF, need for acute treatment or observation due to any other reason, as judged by the investigator.

• = Grade 2 vomiting;

• = Grade 2 liver dysfunction/failure (clinical);

• Any abnormality noted on EKG except for asymptomatic sinus arrhythmia

• History of allergy/sensitivity to sodium phenylbutyrate

• Use of sodium phenylbutyrate within 30 days of study entry

• Serious illness requiring systemic treatment and/or hospitalization within 14 days prior to study entry (Subjects are not eligible following serious illness until therapy is complete and the subject is stable, or until the subject is on therapy and stable for at least 14 days.)

• Poor respiratory status which is expected to require the initiation of BiPAP during the initial 29 days of drug administration.

• Use of medications intended for the treatment of SMA including riluzole, valproic acid, hydroxyurea, oral use of albuterol, sodium phenylbutyrate, butyrate derivatives, creatine, carnitine, growth hormone, anabolic steroids, probenecid, oral or parenteral use of corticosteroids at entry, haloperidol, agents anticipated to increase or decrease muscle strength or agents with known or presumed histone deacetylase (HDAC) inhibition within 30 days prior to study entry.

Notes: Subjects who use a nebulizer or require an inhaler to receive albuterol will be allowed in the study; however oral use of albuterol is prohibited. Topical use of steroids will be allowed. Oral use of steroids is not allowed at entry, but these may be used as clinically indicated while on study. Event grading will be based on the toxicity-grading table in the protocol.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Atrophy
• Muscular Atrophy
• Muscular Atrophy, Spinal
• Spinal Muscular Atrophy Type I

Intervention

Drug:
• sodium phenylbutyrate
500 mg/kg/day, depending upon tolerability subsequent dosages may increase to 675, 900, or 1200 mg/kg/day to identify maximum tolerated dose (MTD) and then an additional 6 participants will enroll at the MTD.

Locations

Country	Name	City	State
United States	Children's Hospital, Boston, 300 Longwood Avenue, Fegan 11	Boston	Massachusetts
United States	University of Texas Southwestern Medical Center at Dallas, Division of Pediatric Neurology, Children's Medical Center of Dallas, Ambulatory Care Pavilion, 2350 Stemmons Freeway, Suite #5074	Dallas	Texas
United States	Columbia University, 180 Fort Washington Avenue, 5th Floor	New York	New York
United States	The Children's Hospital of Philadelphia, Clinical Trials Office, A-230, 34th St. and Civic Center Boulevard	Philadelphia	Pennsylvania
United States	Stanford University Medical Center, 300 Pasteur Drive, Room A343	Stanford	California

Sponsors (2)

Lead Sponsor	Collaborator
Westat	National Institute of Neurological Disorders and Stroke (NINDS)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose Limiting Toxicities (DLT)	Number of DLTs to determine the maximum tolerated dosage. A DLT is defined as any Grade(GR)3 or higher adverse event, GR 1 or higher cardiac arrhythmia; GR 2 or higher vomiting; GR 2 or higher liver dysfunction/failure (clinical); GR 2 elevation of amylase or lipase accompanied by clinical symptoms of pancreatitis. The following GR 2 events are classified as DLTs if evaluated to be clinically significant by the principal investigator or medical safety monitor: decrease of hemoglobin, WBCs, platelets; elevation of AST, ALT, bilirubin; abnormlity of Na, K, Cl, CA, HCO3, glucose, BUN, creatinine.	29 days	Yes
Primary	Survival Motor Neuron (SMN) Messenger Ribonucleic Acid (mRNA)	The change of level in blood SMN mRNA from baseline to assess time course and dose response.	Baseline - 12 weeks	No
Primary	Survival Motor Neuron (SMN) Protein	The change of level in blood SMN protein from baseline to assess time course and dose response.	Baseline - 12 Weeks	No
Secondary	Drug Safety	Adverse event (AE) monitoring	14 weeks	Yes
Secondary	Pharmacokinetic Parameters (Maximum Plasma Concentration)	Maximum Plasma Concentration (Cmax)	12 weeks	No
Secondary	Pharmacokinetic Parameters (Time to Maximum Plasma Concentration)	Time to maximum plasma concentration (Tmax)	12 weeks	No
Secondary	Pharmacokinetic Parameters (Area Under the Plasma Concentration Versus Time Curve (AUC))	Area under the plasma concentration versus time curve (AUC)	12 weeks	No
Secondary	Overall Study Drug Compliance	Subjects receiveing 80% or more of the prescribed doses within each study visit interval were considered compliant.	12 weeks	No