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Clinical Trials/NCT01485965
NCT01485965
Completed
Phase 1

A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196

Siena Biotech S.p.A.7 sites in 1 country26 target enrollmentNovember 2011
InterventionsSEN0014196

Overview

Phase
Phase 1
Intervention
SEN0014196
Conditions
Huntington's Disease
Sponsor
Siena Biotech S.p.A.
Enrollment
26
Locations
7
Primary Endpoint
To determine the effect of food on the repeated dose pharmacokinetics of SEN0014196 at 100 mg once daily in subjects with Huntington's disease
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The primary purpose of this study is to assess the effect of food upon the pharmacokinetics (PK) of SEN0014196 in subjects with Huntington disease (HD).

Detailed Description

In addition to the pharmacokinetic endpoints, the study will assess the safety and tolerability of 100 mg once daily (qd) doses of SEN0014196 over 14 days in subjects with HD and explore potential biomarkers for use in subsequent Phase 2/3 studies.

Registry
clinicaltrials.gov
Start Date
November 2011
End Date
December 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Siena Biotech S.p.A.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects with early to mid HD, i.e., genetically confirmed HD (cytosine, adenine, guanine \[CAG\] codon repeat length ≥ 36), motor signs of HD, and a Total Functional Capacity Subscale Score (TFC) ≥ 7
  • Body mass index between 18 and 31 kg/m2 inclusive
  • All subjects must have a body weight greater than 50 kg
  • Female subjects must be surgically sterile, postmenopausal, or willing to practice a highly effective method of contraception. All female participants must be nonlactating and nonpregnant. Male subjects must agree to use a reliable method of birth control during the study and for 3 months after the last dose of study drug.
  • Capable of providing informed consent
  • Subjects must have a live-in competent observer

Exclusion Criteria

  • Participation in a study or received an investigational drug within 30 days of the Baseline Visit
  • Any prior or concomitant use of compounds suspected of interfering with protein acetylation
  • Any concomitant use of medications that are known inhibitors of CYP450 enzymes or substrates of CYP1A2 at the time of enrollment
  • Suicide risk, as determined by meeting either of the following criteria: a) a suicide attempt within the past year or suicidal ideation within 60 days of the Screening Visit; b) Significant risk of suicide, as judged by the Investigator
  • Subjects with MMSE \< 24
  • Subjects with presence of clinically significant psychosis and/or confusional states, in the opinion of the Investigator
  • Subjects with clinically significant laboratory or ECG abnormalities at Screening or Baseline
  • Subjects with clinically relevant hematologic, hepatic, cardiac, or renal disease
  • Subjects with a current or past (within the last 12 months) history of epilepsy or seizures
  • A medical history of infection with human immunodeficiency virus, hepatitis C, and/or hepatitis B

Arms & Interventions

Fasted condition

Subjects in the Fasted group will take study drug after an overnight fast (since at least midnight). Additionally, on PK assessment days, no food will be allowed for at least 4 hours after study drug administration.

Intervention: SEN0014196

Fed condition

Subjects in the Fed group will take study drug within 30 minutes after starting breakfast; these subjects will otherwise maintain their normal eating schedule.

Intervention: SEN0014196

Outcomes

Primary Outcomes

To determine the effect of food on the repeated dose pharmacokinetics of SEN0014196 at 100 mg once daily in subjects with Huntington's disease

Time Frame: 14 Days

The effect of food on the PK of SEN0014196 will be evaluated for the following parameters: maximum observed plasma concentration (Cmax), time of maximum observed plasma concentration(tmax), AUC from time zero to the length of the dosing interval (tau) (AUC0-τ), AUC from time zero to the last quantifiable concentration (AUC0-last), AUC from time zero to infinity (AUC0-∞), terminal elimination half-life (t1/2), and terminal elimination rate constant (λz).

Secondary Outcomes

  • Pharmacodynamics(14 Days)
  • To determine the safety and tolerability of repeated doses of SEN0014196 at 100 mg once daily in subjects with Huntington's disease(14 Days)

Study Sites (7)

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