An Open Label Extension Study in Subjects With Fragile X Syndrome

Fragile X Syndrome Clinical Trial

— 209FX303  

Official title:

An Open-Label Extension Study to Evaluate the Safety, Tolerability, and Pharmacokinetics in Subject With Fragile X Syndrome

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01555333
• Other study ID #: 209FX303
• Status: Terminated
• Phase: Phase 3
• First received: March 1, 2012
• Last updated: July 30, 2013
• Start date: November 2011
• Est. completion date: July 2013

Study information

• Verified date: July 2013
• Source: Seaside Therapeutics, 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 enroll subjects who have completed Protocols 209FX301, 209FX302, or are currently participating in Protocol 2202 into a long-term study in which all subjects will receive active drug (arbaclofen).

Description:

Three studies sponsored by Seaside Therapeutics, Inc., are currently evaluating the efficacy of STX209 for management of typical problem behaviors in subjects with FXS. These are Study 209FX301, "A Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy, Safety, and Tolerability of STX209 (Arbaclofen) Administered for the Treatment of Social Withdrawal in Adolescents and Adults with Fragile X Syndrome;" Study 209FX302, "A Randomized, Double-Blind, Placebo-Controlled, Fixed- Dose Study of the Efficacy, Safety, and Tolerability of STX209 (Arbaclofen) Administered for the Treatment of Social Withdrawal in Children with Fragile X Syndrome;" and Study 22002, "An Open-Label Extension Study to Evaluate the Safety, Tolerability and Pharmacokinetics of STX209 in Subjects with Fragile X Syndrome." This study will enroll subjects who have completed Protocols 209FX301, 209FX302, or are currently participating in Protocol 22002 into a long-term, open-label study. The open-label extension protocol will provide data on the long-term safety and tolerability of STX209 among subjects with FXS who receive treatment under conditions reflective of their typical medical care rather than in their previously completed study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 357
• Est. completion date: July 2013
• Est. primary completion date: July 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 5 Years to 50 Years

Eligibility

Inclusion Criteria:

1. Successfully completed all scheduled visits of the previous protocol ( 22002, 209FX301, or 209FX302).

2. A parent,LAR, or caregiver must be willing and able to accompany the subject to all study visits, participate in phone calls, complete study assessments, administer study medication, and report the subject's condition and medication use to site staff members.

3. Prior to the conduct of any study-specific procedures, the subject must provide written informed consent to participate in the study ( if developmentally appropriate) or verbal assent and the parent/caregiver/LAR must provide written informed consent. If the caregiver attending the clinic visits is not the parents, caregiver, or LAR, written consent must also be obtained for the caregiver's participation in the study.

4. Current treatment with no more than 3 psychoactive medications, including anti-epileptics, unless the Medical Monitor is consulted.

5. Subjects with a history of seizure disorder must have been seizure free for 6 months and be taking anti-epileptics, or seizure free for 3 years if not receiving anti-epileptic treatment. If currently receiving treatment with anti-epileptics, serum concentration levels must be tested and be in therapeutic range.

6. Negative pregnancy test for females of childbearing potential or be using a medically acceptable form of birth control.

Exclusion Criteria

1. Subjects with any condition that might interfere with the conduct of the study, confound interpretation of the study results, or endanger their own well-being. This includes, but is not limited to impairment of renal function, evidence or history of malignancy or any significant hematological, endocrine, cardiovascular, respiratory, hepatic, or gastrointestinal disease.

2. Subjects who are currently engaged in illicit drug or alcohol abuse.

3. Subjects who had a serious adverse event (SAE) while taking STX209 during their previous protocol (22002,209FX301,309FX302)that the Investigator considered related to STX209, unless approval from the Medical Monitor is obtained.

4. The occurrence or continuation of any AE or condition during Studies 22002, 209FX301, or 209FX302 that, in the opinion of the Investigator, should exclude this subject from participating in the open-label extension.

5. Subjects taking another investigational drug, other than STX209, currently or within 30 days of Visit 1. Subject must not take any investigational drugs during this study.

6. Subjects who, in the Investigator's opinion, might not be suitable for the study.

7. Subjects treated with vigabatrin, tiagabine, or riluzole currently or within 2 weeks of Visit 1.

8. Subjects treated with racemic baclofen currently or within 1 week of Visit 1.

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Fragile X Syndrome
• Syndrome

Intervention

Drug:
• arbaclofen
A flexible dose titration will be utilized. Orally disintegrating tablets

Locations

Country	Name	City	State
United States	Seaside Therapeutics Site #05	Akron	Ohio
United States	Seaside Therapeutics Site #17	Aurora	Colorado
United States	Seaside Therapeutics Site #12	Baltimore	Maryland
United States	Seaside Therapeutics Site #24	Chapel Hill	North Carolina
United States	Seaside Therapeutics Site #02	Chicago	Illinois
United States	Seaside Therapeutics Site #03	Columbia	Missouri
United States	Seaside Therapeutics Site #20	Decatur	Georgia
United States	Seaside Therapeutics Site #21	Durham	North Carolina
United States	Seaside Therapeutics Site #25	Houston	Texas
United States	Seaside Therapeutics Site #23	Kansas City	Kansas
United States	Seaside Therapeutics Site #07	Long Beach	California
United States	Seaside Therapeutics Site #11	Media	Pennsylvania
United States	Seaside Therapeutics Site #01	Miami	Florida
United States	Seaside Therapeutics Site #19	Nashville	Tennessee
United States	Seaside Therapeutics Site #22	New York	New York
United States	Seaside Therapeutics Site #15	Oklahoma City	Oklahoma
United States	Seaside Therapeutics Site #14	Orange City	Florida
United States	Seaside Therapeutics Site #16	Phoenix	Arizona
United States	Seaside Therapeutics Site #10	Sacramento	California
United States	Seaside Therapeutics Site #18	San Antonio	Texas
United States	Seaside Therapeutics Site #13	Seattle	Washington
United States	Seaside Therapeutics Site #04	Staten Island	New York
United States	Seaside Therapeutics Site #08	Worcester	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Seaside Therapeutics, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety Measures	Adverse Events, Suicidality Assessment, Physical Examination, Vital Signs and Weight, Laboratory Tests: Complete Blood Count, Urinalysis, Chemistry Panel	100 weeks	Yes
Secondary	Efficacy	Aberrant Behavior Checklist Lethargy/Social Withdrawal Sub- Scale Clinical Global Impression Vineland Adaptive Behavior Scales Stanford Binet Intelligence Scale	100 Weeks	No