Clinical Study of Droxidopa in Patients With Neurogenic Orthostatic Hypotension (NOH)

Dopamine Beta Hydroxylase Deficiency Clinical Trial

— NOH302  

Official title:

Phase III, Multi-Center, Study to Assess the Clinical Effect of Droxidopa in Subjects With Primary Autonomic Failure, Dopamine Beta Hydroxylase Deficiency or Non-Diabetic Neuropathy and Symptomatic NOH

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00633880
• Other study ID #: Droxidopa NOH302
• Status: Completed
• Phase: Phase 3
• First received: March 5, 2008
• Last updated: April 22, 2014
• Start date: January 2008
• Est. completion date: September 2009

Study information

• Verified date: April 2014
• Source: Chelsea Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationCanada: Health CanadaUnited Kingdom: Medicines and Healthcare Products Regulatory AgencyPoland: Office for Registration of Medicinal Products, Medical Devices and Biocidal ProductsAustralia: Department of Health and Ageing Therapeutic Goods Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to see whether droxidopa is effective in treating symptoms of neurogenic orthostatic hypotension in patients with Primary Autonomic Failure (Pure Autonomic Failure, Multiple System Atrophy, Parkinson's Disease), Non-diabetic neuropathy, or Beta Hydroxylase deficiency.

Description:

Systolic blood pressure is transiently and minimally decreased in healthy individuals upon standing. Normal physiologic feedback mechanisms work through neurally-mediated pathways to maintain the standing blood pressure, and thus maintain adequate cerebral perfusion. The compensatory mechanisms that regulate blood pressure upon standing are dysfunctional in subjects with orthostatic hypotension (OH), a condition that may lead to inadequate cerebral perfusion with accompanying symptoms of syncope, dizziness or lightheadedness, unsteadiness and blurred or impaired vision, among other symptoms.

The autonomic nervous system has a central role in the regulation of blood pressure. Primary Autonomic Failure is manifested in a variety of syndromes. Orthostatic hypotension is a usual presenting symptom. Primary Autonomic Failure may be the primary diagnosis, and classifications include pure autonomic failure (PAF), also called idiopathic orthostatic hypotension (Bradbury-Eggleston syndrome) autonomic failure with multiple system atrophy (Shy-Drager syndrome) and also Parkinson's disease. Regardless of the primary condition, autonomic dysfunction underlies orthostatic hypotension.

Orthostatic hypotension may be a severely disabling condition which can seriously interfere with the quality of life of afflicted subjects. Currently available therapeutic options provide some symptomatic relief in a subset of subjects, but are relatively ineffective and are often accompanied by severe side effects that limit their usefulness. Support garments (tight-fitting leotard) may prove useful in some subjects, but is difficult to don without family or nursing assistance, especially for older subjects. Midodrine, fludrocortisone, methylphenidate, ephedrine, indomethacin and dihydroergotamine are among some of the pharmacological interventions that have been used to treat orthostatic hypotension, although only midodrine is specifically approved for this indication. The limitations of these currently available therapeutic options, and the incapacitating nature and often progressive downhill course of disease, point to the need for an improved therapeutic alternative.

The current withdrawal design study will measure the efficacy of droxidopa on symptoms of neurogenic orthostatic hypotension in patients randomized to continued droxidopa treatment versus placebo, following 14 days of double-blind treatment.

droxidopa

droxidopa [also, known as L-threo-3,4-dihydroxyphenylserine, L-threo-DOPS, or L-DOPS] is the International non-proprietary name (INN) for a synthetic amino acid precursor of norepinephrine (NE), which was originally developed by Sumitomo Pharmaceuticals Co., Limited, Japan. It has been approved for use in Japan since 1989. Droxidopa has been shown to improve symptoms of orthostatic hypotension that result from a variety of conditions including Shy Drager syndrome (Multiple System Atrophy), Pure Autonomic Failure, and Parkinson's disease. There are four stereoisomers of DOPS; however, only the L-threo-enantiomer (droxidopa) is biologically active.

The exact mechanism of action of droxidopa in the treatment of symptomatic NOH has not been precisely defined; however, its NE replenishing properties with concomitant recovery of decreased noradrenergic activity are considered to be of major importance.

Droxidopa has been marketed in Japan since 1989. Data from clinical studies and post-marketing surveillance programs conducted in Japan show that the most commonly reported adverse drug reactions with droxidopa are increased blood pressure, nausea, and headache. In clinical studies, the prevalence and severity of droxidopa adverse effects appear to be similar to those reported by the placebo control arm.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 181
• Est. completion date: September 2009
• Est. primary completion date: August 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

PATIENT INCLUSION CRITERIA:

• Male or female and aged 18 years or over;

• Clinical diagnosis of orthostatic hypotension associated with Primary Autonomic Failure (PD, MSA and PAF), Dopamine Beta Hydroxylase Deficiency or Non-Diabetic Autonomic Neuropathies;

• A documented fall in systolic blood pressure of at least 20 mmHg, or in diastolic blood pressure of at least 10 mmHg, within 3 minutes after standing;

• Provide written informed consent to participate in the study and understand that they may withdraw their consent at any time without prejudice to their future medical care.

MAIN PATIENT EXCLUSION CRITERIA:

• Taking ephedrine or midodrine; Patients taking ephedrine or midodrine may enroll after a minimum 7 day washout period;

• Taking anti-hypertensive medication;

• Have a history of more than moderate alcohol consumption;

• Women who are pregnant or lactating;

• Have a history of closed angle glaucoma;

• Have pre-existing sustained severe hypertension (BP > 180/110 mmHg in the sitting position);

• Have atrial fibrillation or, in the investigator's opinion, have any other significant cardiac arrhythmia;

• In the investigator's opinion, have any other significant systemic, hepatic, cardiac or renal illness;

• Have diabetes mellitus or insipidus;

• Have a known or suspected malignancy;

• Have known gastrointestinal illness or other gastrointestinal disorder that may, in the investigator's opinion, affect the absorption of study drug;

• In the investigator's opinion, have clinically significant abnormalities on clinical examination or laboratory testing;

• Have a serum creatinine level > 130 µmol/L;

Study Design

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

Related Conditions & MeSH terms

• Autonomic Nervous System Diseases
• Dopamine Beta Hydroxylase Deficiency
• Hypotension
• Hypotension, Orthostatic
• Non-diabetic Neuropathy
• Primary Autonomic Failure
• Pure Autonomic Failure
• Symptomatic Neurogenic Orthostatic Hypotension (NOH)

Intervention

Drug:
• Placebo
100 mg, oral, three times per day 200 mg, oral, three times per day 300 mg, oral, three times per day 400 mg, oral, three times per day 500 mg, oral, three times per day 600 mg, oral, three times per day
• Droxidopa
100 mg, oral, three times per day 200 mg, oral, three times per day 300 mg, oral, three times per day 400 mg, oral, three times per day 500 mg, oral, three times per day 600 mg, oral, three times per day

Locations

Country	Name	City	State
Australia	Royal Adelaide Hospital	Adelaide	South Australia
Australia	Austin Hospital	Heidelburg
Australia	Baker Heart Research Institute	Melbourne	Victoria
Canada	McMaster University	Hamilton	Ontario
Canada	Centre for Movement Disorders	Markham	Ontario
Canada	SMBD Jewish General Hospital	Montreal	Quebec
Canada	Parkinson's & Neurodegenerative Disorders Clinic	Ottawa	Ontario
Canada	Quebec Memory and Motor Skills Disorders Clinic	Quebec
New Zealand	Van der Veer Institute for Parkinson's Disease and Movement Disorders	Christchurch
New Zealand	Auckland Hospital	Grafton Auckland	Private Bag
United States	University of Maryland	Baltimore	Maryland
United States	Jacinto Medical Group, PA	Baytown	Texas
United States	University of Alabama at Birmingham	Birmingham	Alabama
United States	Parkinson's Disease & Movment Disorder Center	Boca Raton	Florida
United States	Beth Israel Deaconess Medical Center	Boston	Massachusetts
United States	Medical Associates of North Georgia	Canton	Georgia
United States	Saint Mary of Nazareth Hospital Center	Chicago	Illinois
United States	University of Cincinnati	Cincinnati	Ohio
United States	Cleveland Clinic	Cleveland	Ohio
United States	University Hospitals Case Medical Center	Cleveland	Ohio
United States	Electrophysiology Associates	Colorado Springs	Colorado
United States	UT Southwestern Medical Center	Dallas	Texas
United States	Duke University Medical Center	Durham	North Carolina
United States	New Jersey Neuroscience Institute	Edison	New Jersey
United States	Indiana Medical Research	Elkhart	Indiana
United States	The Parkinson's and Movement Disorders Institute	Fountain Valley	California
United States	Southeastern Integrated Medical	Gainesville	Florida
United States	JWM Neurology	Indianapolis	Indiana
United States	Mayo Jacksonville Florida Department of Neurology	Jacksonville	Florida
United States	Kingston Neurological Associates, PC	Kingston	New York
United States	Dedicated Clinical Research	Litchfield Park	Arizona
United States	University of Louisville	Louisville	Kentucky
United States	University of Miami	Miami	Florida
United States	Vanderbilt University	Nashville	Tennessee
United States	Columbia University	New York	New York
United States	NYU Medical Center	New York City	New York
United States	North Chicago VA Medical Center	North Chicago	Illinois
United States	COR Clinical Research, LLC	Oklahoma City	Oklahoma
United States	Kansas City Bone and Joint, PA	Overland Park	Kansas
United States	Pacific Neuroscience Medical Group	Oxnard	California
United States	Xenoscience Inc.	Phoenix	Arizona
United States	The Oregon Clinic	Portland	Oregon
United States	Mayo Clinic Rochester	Rochester	Minnesota
United States	University of Rochester	Rochester	New York
United States	Scott & White Healthcare - Round Rock	Round Rock	Texas
United States	Henry Ford Health System	Southfield	Michigan
United States	Washington University Medical Center	St. Louis	Missouri
United States	Sun Health Research Institute	Sun City	Arizona
United States	The Parkinson's Institute	Sunnyvale	California
United States	University of South Florida	Tampa	Florida
United States	Scott & White Memorial Hospital & Clinic	Temple	Texas
United States	East Texas Medical Center	Tyler	Texas
United States	Wake Forest University	Winston Salem	North Carolina
United States	University of Massachusetts Worcester	Worcester	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Chelsea Therapeutics	Chiltern International Inc.

Countries where clinical trial is conducted

United States,  Australia,  Canada,  New Zealand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Dizziness/ Lightheadedness/ Feeling Faint/ or Feeling Like You Might Blackout (OHSA Item 1)	OHSA item 1 scale range: 0 (none) -10 (worst), likert scale. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No
Secondary	Change in Fatigue (OHSA Item 4)	OHSA item 4 scale range: 0 (none) -10 (worst), likert scale. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No
Secondary	Change in Weakness (OHSA Item 3)	OHSA item 3 scale range: 0 (none) -10 (worst), likert scale. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No
Secondary	Change in Vision (OHSA Item 2)	OHSA item 2 scale range: 0 (none) -10 (worst), likert scale. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	Yes
Secondary	Change in Concentration (OHSA Item 5)	OHSA item 5 scale range: 0 (none) -10 (worst), likert scale. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No
Secondary	Change in Head/Neck Discomfort (OHSA Item 6)	OHSA item 6 scale range: 0 (none) -10 (worst), likert scale. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No
Secondary	Change in Ability to Conduct Activities of Daily Living Score (OHDAS Composite Score)	The OHDAS scale is the average of four items: 1) Standing for a short time; 2) Standing for a long time; 3) Walking for a short time; and 4) Walking for a long time. Each asks the patient to rate their disease impact over the past week. Each item is scored on a Likert scale from 0 to 10, with 10 being the most severe. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No
Secondary	Change in Orthostatic Hypotension Symptom Assessment Score (OHSA Composite)	The OHSA scale is the average of six items: 1) Dizziness, lightheadedness, feeling faint or feeling like you might black out; 2) Problems with vision; 3) Weakness; 4) Fatigue; 5) Trouble concentrating; and 6) Head/neck discomfort. Each asks the patient to rate their symptoms over the past week. Each item is scored on a Likert scale from 0 to 10, with 10 being the most severe. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No
Secondary	Change in Orthostatic Hypotension Symptom Scores Excluding Dizziness (OHSA Composite Items 2-6)	OHSA composite scale (items 2-6) is the average of five OHSA items: 2) Problems with vision; 3) Weakness; 4) Fatigue; 5) Trouble concentrating; and 6) Head/neck discomfort. Each asks the patient to rate their symptoms over the past week. Each item is scored on a Likert scale from 0 to 10, with 10 being the most severe. Change: score at end of study minus score at randomization. In this withdrawal design, a positive score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No
Secondary	Change in Systolic Blood Pressure (SBP) Measurements 3 Minutes Post Standing;	Change: standing systolic blood pressure at end of study minus standing systolic blood pressure at randomization. In this withdrawal design, a negative score indicates worsening during the double-blind randomized phase relative to value at randomization (on open-label drug) .	14 days	No