Study Purpose:
The FLX-787-106 study will determine how well FLX-787-ODT works to reduce fasciculations in patients with Amyotrophic Lateral Sclerosis (ALS). The study will measure how often fasciculations occur, and monitor any side effects that might develop while taking the investigational product. Participants will be assessed before and after taking a single dose of FLX-787-ODT. Approximately 15 people will take part in this study at one center in the United States. Participants will be in the study for a single clinic visit and receive a telephone call 7 days later to monitor for side effects.Study Status:
Not recruiting
Disease:
Amyotrophic Lateral Sclerosis , Fasciculation
Study Type:
Interventional
Type of Intervention:
Drug
Intervention Name:
FLX-787-ODT (orally disintigrating tablet)
Placebo:
No
Phase:
Phase 1/Phase 2
Study Chair(s)/Principal Investigator(s):
N/A
Clinicaltrials.gov ID:
Neals Affiliated?
No
Coordinating Center Contact Information
United States
Study Sponsor:
Flex Pharma, Inc.
Estimated Study Start Date:
11 / 01 / 2017
Estimated Study Completion Date:
08 / 01 / 2018
Posting Last Modified Date:
01 / 23 / 2018
Date Study Added to neals.org:
11 / 09 / 2017
This study was withdrawn (sponsor decision)
Minimum Age:
18 Years
Maximum Age:
N/A
Can participants use Riluzole?
Yes
Inclusion Criteria:- Documented diagnosis of ALS diagnosis of less than 3 years.
- Expected survival > 6 months
- Frequent fasciculations noted during clinical examination of any single muscle (>6 visible fasciculations per minute) observed in Part I
- Normal oral cavity exam at screening
- Proficient in English
- Male subjects will either be surgically sterile or agree to use a medically acceptable method of contraception during sexual contact with females of childbearing potential, and will refrain from sperm donation for 45 days following the study
- Male subjects will either be surgically sterile or agree to use a medically acceptable method of contraception during sexual contact with females of childbearing potential, and will refrain from sperm donation for 45 days following the study
Exclusion Criteria:
- Presence of clinically significant or unstable condition that would result in an increased risk of study participation or difficulty in interpretation of the study results
- Tremor or other movement disorder that would interfere with recording
- Inability to lie flat
- Presence of major gastrointestinal disorders, such as inflammatory bowel disease, diverticulitis, active peptic ulcer disease, or significant gastroesophageal reflux disease (i.e., not well-controlled on antacids or proton pump inhibitors), or oral or esophageal lesions/ulcers
- Presence of laryngospasm or significant swallowing problems
- Presence of percutaneous endoscopic gastrostomy, esophagogastroduodenoscopy, or G-tube
- Inability to tolerate a spicy sensation in the mouth or stomach
- Actively using illicit drugs or history of chronic substance abuse within the past year prior to screening, including abuse of alcohol
- Participated in a clinical study (except natural history studies without administration of an investigational product) within 30 days prior to screening
- Pregnant, breastfeeding, or planning to become pregnant
- Blood pressure of ≥160 mmHg systolic and/or ≥100 mmHg diastolic
- Clinically significant abnormalities in laboratory findings (including screening complete electrolyte panel, complete blood count, liver function tests).
Wake Forest University Health Sciences
Winston-Salem, North Carolina
27157
United States