Efficacy Study of NH001 in Vegetative State & Minimally Conscious State Following a Traumatic Brain Injury

NCT ID: NCT00761228

Last Updated: 2017-03-31

Basic Information

• Recruitment Status: SUSPENDED
• Clinical Phase: PHASE2
• Total Enrollment: 76 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-07-31
• Study Completion Date: 2018-12-31

Brief Summary

The purpose of this study is to test the drug apomorphine in subjects who are in a Vegetative State or a Minimally Conscious State.

Detailed Description

This is a prospective, multi-center, randomized, double-blind, placebo-controlled study of the safety and efficacy of NH001 to improve the functional outcome of patients in a vegetative state or minimally conscious state following a severe traumatic brain injury (TBI).

Conditions

Brain Injury

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Apomorphine

Patients will receive an ascending dosing schedule to reach a maximum infusion rate of up to 6 mg/hour for 12 hours a day.

Group Type: ACTIVE_COMPARATOR

Apomorphine

Intervention Type: DRUG

Patients will receive an ascending dosing schedule of continuous subcutaneous apomorphine to reach a maximum infusion rate of up to 6 mg/hour for 12 hours a day.

Placebo

Patients will receive a continues subcutaneous infusion of saline solution.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Patients will receive a continues subcutaneous infusion of saline solution.

Interventions

Apomorphine

Patients will receive an ascending dosing schedule of continuous subcutaneous apomorphine to reach a maximum infusion rate of up to 6 mg/hour for 12 hours a day.

Intervention Type: DRUG

Placebo

Patients will receive a continues subcutaneous infusion of saline solution.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patient is between 18 and 50 years of age, inclusive.

2. Male or non-pregnant female (females of child-bearing potential will be required to have undergone a pregnancy test with negative results prior to entry to the study).

3. Patients will have sustained a severe closed head injury within one to four months.

4. Patients will have remained in a vegetative or minimally conscious state between one and four months after injury.

5. Patients will have reached a stabilized clinical state prior to admission to the study (e.g. afebrile, haemodynamic and electrolyte stability).

6. Patients will have a mean DRS score between 17 and 29, when measured twice a day over two consecutive days.

7. Informed consent from a legal representative will have been obtained, according to the procedures outlined in Section 8.1.2.

8. Patients who, according to the investigator's opinion, are likely to be available for the required 180-day follow up evaluation.

Exclusion Criteria

1. Patients who are not clinically stable at the time of entry into the study (infections, cardiovascular decompensation, etc.)

2. Patients who require mechanical respiratory assistance.

3. Patients who show signs of progressive neurological deterioration post-TBI.

4. Patients with a known history of medically relevant substance abuse.

5. Patients with history of cardiac disease.

6. Patients who suffered an anoxic event.

7. Patients who have received an investigational drug within 30 days of the study.

8. Patients who have previously used NH001, other dopaminergic agent (e.g. levodopa, amantadine, domperidone) or any known neuro-stimulant (e.g. methylphenidate, amphetamines, atomoxetine, modafinil) within the last 7 days days.

9. Patients who are receiving dopamine blockers (e.g. risperidone, haloperidol, chlorpromazine, flupenthixol, clozapine, olanzapine, quetiapine)

10. Patients who are receiving drugs of the 5HT3 antagonist class, including, for example, ondansetron, granisetron, dolasetron, palonosetron and alosetron.

11. Patients who are receiving tricyclic antidepressants drugs

12. Patients who are receiving type I antiarrhythmics (i.e. quinidine).

13. Patients who have a known history of cardiac arrhythmias or congenital QTc prolongation.

14. Patients who have a known history of previous neurological functional impairment (e.g. stroke, spinal cord injury, dementia, epilepsy, psychiatric diseases).

15. Patients who experienced seizures within the first week post injury or have ongoing seizures.

16. Patients receiving prophylactic anti-convulsive medications.

17. Patients with known allergies to apomorphine, morphine, sulfites or trimethobenzamide.

18. Patients who are receiving nitrates or other vasodilators.

19. Patients receiving CNS acting agents such as barbiturates, morphine, belladonna, opiates.

20. For male patients, patients who are receiving trazodone or any other drug that is known to produce priapism.

21. Patients without a relative or legal guardian to consent to the study.

22. Patients who, according to the investigator's opinion, are unlikely to be available for the required 180-day follow up evaluation.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

FDA Office of Orphan Products Development

FED

Sponsor Role: collaborator

NeuroHealing Pharmaceuticals Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Elkan R Gamzu, PhD

Role: PRINCIPAL_INVESTIGATOR

NeuroHealing Pharmaceuticals Inc.

Ross D Zafonte, DO

Role: PRINCIPAL_INVESTIGATOR

Spaulding Rehabilitation Hospital

Locations

Spaulding Rehabilitation Hospital

Boston, Massachusetts, United States

Countries

United States

Other Identifiers

3337

Identifier Type: -

Identifier Source: org_study_id