The Effects of Fx-1006A on Transthyretin Stabilization and Clinical Outcome Measures in Patients With Non-V30M Transthyretin Amyloidosis

PHASE2CompletedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

June 30, 2008

Primary Completion Date

January 31, 2010

Study Completion Date

January 31, 2010

Conditions
Transthyretin-associated Amyloidosis With Polyneuropathy
Interventions
DRUG

Fx-1006A

During Part 1, patients will receive Fx-1006A 20mg soft gelatin capsules once daily (at the same time each day) for two weeks. During Part 2, patients will receive Fx-1006A 20mg soft gelatin capsules once daily to complete a total of 12 months of dosing

Trial Locations (4)

21205

Johns Hopkins Hospital, Baltimore

Unknown

CHU de Bicetre, Paris

Universitatsklinikum Munster, Transplant Hepatology, Münster

19 - 27100

Centro per lo Studio e la Cura delle Amiloidosi Sistemiche, Irccs - Policlinico San Matteo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY