Recent Updates
Recently added Catalysts

Rifaximin 550 milligrams

Phase 2

Alzheimer's Disease | Small Molecules | Neurology |Bausch Health Companies Inc.|Trials Updated: Dec 17, 2021

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment10

FDA Designations

No designations recorded

Rifaximin 550 milligrams clinical trials

Rifaximin 550 milligrams · 1 trial · 1 indication

Phase 2 1
NCT03856359Trial of Rifaximin in Probable Alzheimer's DiseaseAlzheimer's Disease
COMPLETED10 Analytics
PHASE2COMPLETED
Trial of Rifaximin in Probable Alzheimer's Disease
Alzheimer's DiseaseUnlock trial analytics

Study Endpoints

Primary Endpoints

Number of Participants Experiencing Diarrhea Caused by Clostridium Difficile
5 months

Collected at every visit and follow-up phone visits. A rare side effect of Rifaximin is diarrhea caused by clostridium difficile. This is a very serious form of diarrhea that can be fatal if not treated. The investigators will be following the patients closely during treatment and for 2 months following treatment to see if the patient has any signs or symptoms of this diarrhea. If a patient does develop clostridium difficile diarrhea, they will be promptly treated.

Change in ADAS Cog 11 Scores
At baseline and at 3 months

Change in Alzheimer's Disease Assessment Scale - Cognition test with 11 tasks (ADAS Cog 11) scores following 3 months of oral Rifaximin. Scores range from minimum 0 - maximum 70. Higher scores mean worse outcome.

Secondary Endpoints

Change in Tolerability as Measured by Number of Adverse Events (AE).
Baseline, 3 months, 5 months
Change in Cognitive Performance on the Mini-Mental State Exam (MMSE)
Baseline, 3 months
Participants With Treatment Emergent Adverse Events as Reported by the Subject That Required a Change in Safety Measures
Safety will be measured through adverse events throughout study, at month 3 and by phone call at month 5 (2 months after treatment termination).
Unlock Study Endpoints

Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
RifaximinEXPERIMENTALrifaximin 550 milligrams (mg) orally twice daily for 3 months

Interventions

NameTypeDescription
Rifaximin 550 milligrams (MG)DRUGRifaximin (Xifaxan, Salix Pharmaceuticals, Bridgewater, N.J.) (See Package Insert) is a drug that is approved by the FDA for use in humans for the treatment of Hepatic Encephalopathy, Traveler's Diarrhea and Irritable Bowel Syndrome. It is commercially available. It will be used in accordance with approved labeling as pertains to dosage and administration for Hepatic Encephalopathy, contraindications and warnings. However, it will be used investigationally in this trial as rifaximin is not FDA approved for the treatment of Alzheimer's Disease.
Unlock Study Design Details

Eligibility Criteria

Age Range55 Years to 85 Years
SexALL
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: * · Probable Alzheimer's Disease (National Institute of Neurological Disorders and Stroke (NINDS) criteria), mild to moderate severity * Ages 55-85; both genders * Mini Mental State Exam (MMSE) scores 10-23 * Willing and able to comply with all scheduled clinic visits. ...

Countries:United States
Unlock Eligibility Criteria