Clinical Pharmacology Study of Oral Edaravone in Patients With Amyotrophic Lateral Sclerosis (ALS)

Study Purpose:

To evaluate the pharmacokinetics of single doses of edaravone oral suspension in Patients with Amyotrophic Lateral Sclerosis

Study Status:

Not recruiting

Disease:

Japanese Patients With ALS

Study Type:

Interventional

Type of Intervention:

Drug

Intervention Name:

MT-1186

Placebo:

No

Phase:

Phase 1

Study Chair(s)/Principal Investigator(s):

General Manager, Mitsubishi Tanabe Pharma Corporation

Clinicaltrials.gov ID:

NCT04176224

Neals Affiliated?

No

Coordinating Center Contact Information

Study Sponsor:

Mitsubishi Tanabe Pharma Corporation

Estimated Enrollment:

9

Estimated Study Start Date:

04 / 17 / 2019

Estimated Study Completion Date:

09 / 04 / 2019

Posting Last Modified Date:

11 / 25 / 2019

Date Study Added to neals.org:

11 / 25 / 2019

Minimum Age:

20 Years

Maximum Age:

75 Years

Inclusion Criteria:

The key criteria are listed below.

- Patients aged between 20 and 75 years at the time of informed consent

- Japanese patients

- Among patients with ALS, those "Clinically definite ALS," "Clinically probable ALS" or "Clinically probable-laboratory-supported ALS" according to El Escorial Revised Airlie House criteria

- Patients who can consent to contraception

- Patients who have thoroughly understood the contents of the study and voluntarily provided written informed consent to participate in the study

Exclusion Criteria:

The key criteria are listed below.

- Patients in whom the possibility could not be ruled out that the current symptoms were symptoms of a disease requiring differential diagnosis, such as cervical spondylosis and multifocal motor neuropathy

- Patients undergoing treatment for malignancy

- Patients who have presence of clinically significant liver, heart, or renal disease requiring hospitalization (except ALS) and infections requiring antibiotics. Patients who have a problem in general condition and are judged ineligible by the Investigator

- Body mass index (BMI) of <18.0 or >30.0, or a body weight of <50 kg

- Patients judged by the investigator (or subinvestigator) to be unsuitable for the study for any other reason

Investigational site

Tokyo
Japan