Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease

Sponsor

Omeros Corporation (Industry)

Overall Status

Terminated

CT.gov ID

NCT02074410

Collaborator

(none)

Enrollment

Locations

Arms

9.4

Duration (Months)

2.4

Patients Per Site

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the safety, tolerability and pharmacokinetics of OMS643762 (the study drug) in subjects with Huntington's disease (HD).

Condition or Disease	Intervention/Treatment	Phase
Huntington's Disease	Drug: OMS643762 Drug: Placebo	Phase 2

Study Design

Study Type:

Interventional

Actual Enrollment :

22 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease

Study Start Date :

Jan 1, 2014

Actual Primary Completion Date :

Oct 15, 2014

Actual Study Completion Date :

Oct 15, 2014

Arms and Interventions

Arm	Intervention/Treatment
Experimental: OMS643762 Low Dose without food Orally administering OMS643762 low dose daily without food for 28 days	Drug: OMS643762 Other Names: OMS824
Experimental: OMS643762 Medium Dose without food Orally administering OMS643762 medium dose daily without food for 28 days	Drug: OMS643762 Other Names: OMS824
Experimental: OMS643762 Medium Dose with food Orally administering OMS643762 Medium dose daily with food for 28 days	Drug: OMS643762 Other Names: OMS824
Placebo Comparator: Placebo Orally administering placebo daily for 28 days	Drug: Placebo

Outcome Measures

Primary Outcome Measures

Assess the Safety of OMS643762 [28 days]
Safety as assessed by adverse events
Assess the Safety of OMS643762 [28 days]
Safety as assessed by vital signs
Assess the Safety of OMS643762 [28 days]
Safety as assessed by clinical lab-tests
Assess the Safety of OMS643762 [28 days]
Safety as assessed by ECG
Assess the Safety of OMS643762 [28 days]
Safety as assessed by Columbia-Suicide Severity Rating Scale (C-SSRS)

Secondary Outcome Measures

Motor function [Pre-dose and day 15 and 28 post-dose]
Change from baseline in the UHDRS - Total Motor Score
Motor function [Pre-dose and day 15 and 28 post-dose]
Change from baseline in the Speeded Tapping Test score
Cognition [Pre-dose and day 28 post-dose]
Change from baseline in the Cognitive Assessment Battery composite score
Behavior [Pre-dose and day 28 of dosing]
Change from baseline in the Problem Behavior Assessment score
Pharmacokinetics profile [Pre-dose, day 15 and 28 of dosing and up to 14 days post-dose]
Maximum plasma concentration of OMS643762 following multiple-dose administration

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Voluntarily provide informed consent, or have a legally authorized representative (LAR) provide informed consent with subject assent, in accordance with local regulations and governing Institution Review Board (IRB) requirements prior to any procedures or evaluations performed specifically for the sole purpose of the study (other than the Montreal Cognitive Assessment (MoCA) to assess capacity to provide informed consent). Capacity to provide informed consent will be determined by the MoCA and investigator judgment according to the following:

Subjects with scores of greater than or equal to 21 on the MoCA and, in the judgment of the investigator, have the capacity to provide valid informed consent, can give consent.
Subjects with scores of less than 21 but greater than or equal to 18 on the MoCA and, in the judgment of a mental health professional (independent of the investigator) have the capacity to provide valid informed consent, may give consent.
Subjects with scores less 21 but greater than or equal to 18 on the MoCA, who lack the capacity to give valid informed consent, in the judgment of a mental health professional (independent of the investigator), will need an LAR to provide informed consent with assent by the subject.
Subjects with scores of less than 18 on the MoCA will have an LAR provide informed consent with assent by the subject.

Have a clinical diagnosis of HD, confirmed by either CAG repeat number of greater than or equal to 39 or a positive family history (a first degree relative with a clinical diagnosis of HD) if CAG repeat number is not known.
Are age greater than or equal to 18 and less than or equal to 65 years at the screening visit (Visit 1).
Have a UHDRS Total Functional Capacity greater than or equal to 7 at Visit 1.
If currently taking antipsychotic medication(s), have been on a stable regimen for at least 60 days prior to randomization.
Are fluent in English.
If female, are either a) not of childbearing potential (i.e., surgically sterilized or post-menopausal for more than 1 year) or b) have a negative pregnancy test and if sexually active must agree to use a medically reliable form of contraception throughout the study. Acceptable methods of contraception include a reliable intrauterine device, hormonal contraception or spermicide in combination with a barrier method.
If male, are either a) not of reproductive potential or b) if sexually active must agree to use a medically reliable form of contraception throughout the study. Acceptable methods of birth control include spermicide in combination with a barrier method, or subjects' female partner is willing to use medically acceptable methods of birth control.
Have normal clinical laboratory test results and ECG, or results with minor deviations, which are not considered to be clinically significant by the investigator.

Exclusion Criteria:

Have a history or presence of significant cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, or neurological disorders other than HD which, in the opinion of the investigator, increases the risk of the study drug or may confound the interpretation of study measures.
Have unstable or severe depression, in the opinion of the investigator.
Have alcohol or drug abuse or dependence, as defined by the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision.
Have received treatment with an investigational drug or device within 60 days prior to Visit 1.
Are pregnant or lactating.
Have serum alanine transaminase or aspartate transaminase greater than two times upper limit of normal at screening.
Have hemoglobin, white blood cell count, absolute neutrophil count, or platelet count outside the normal range at screening.
Are an employee of Omeros, an investigator, or study staff member, or their immediate family member.

Contacts and Locations

Locations

	City	State	Country	Postal Code
1	San Diego	California	United States	92037
2	Englewood	Colorado	United States	80113
3	Gainesville	Florida	United States	32607
4	Tampa	Florida	United States	33612
5	Baltimore	Maryland	United States	21287
6	New York	New York	United States	10032
7	Memphis	Tennessee	United States	38163
8	Houston	Texas	United States	77030
9	Kirkland	Washington	United States	98034

Sponsors and Collaborators

Omeros Corporation

Investigators

Study Director: Steve Whitaker, MD, Omeros Corporation

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Omeros Corporation

ClinicalTrials.gov Identifier:

NCT02074410

Other Study ID Numbers:

OMS824-HTD-002

First Posted:

Feb 28, 2014

Last Update Posted:

Oct 22, 2018

Last Verified:

Oct 1, 2018

Additional relevant MeSH terms:

Huntington Disease

Study Results

No Results Posted as of Oct 22, 2018