Short-term Effects of TOLCAPONE on Transthyretin Stability in Subjects With Leptomeningeal TTR Amyloidosis (ATTR)

Early Phase 1

Completed

• Conditions: Amyloidosis, Leptomeningeal, Transthyretin-Related; Transthyretin Amyloidosis
• Interventions: Drug: Tolcapone

• Registration Number: NCT03591757
• Lead Sponsor: Boston University

Brief Summary

The purpose of this study is to determine whether Tolcapone crosses from the blood stream into the fluid around the brain and stabilizes the protein that makes leptomeningeal amyloid. Tolcapone is a commercially available generic drug that treats Parkinson's disease.

The Investigator plans to evaluate Tolcapone as a treatment for ATTR (Transthyretin Amyloidosis), a rare genetic disease often causing death within 5-15 years after diagnosis. ATTR is characterized by deposition of misfolded protein known as amyloid, in one or more organ systems (including the peripheral and autonomic nervous systems, the heart, the brain and the eyes). The age at which symptoms begin to develop varies widely ranging between 20 to 70 years old. ATTR is progressive, and some variants can have a fatal outcome within a few years of presentation. Treatment options include supportive and symptomatic care that may slow or stop progressive decline in functional state but do not alter the pathological process. Liver transplant can be performed in selected patients but is limited by organ supply, requires lifelong immunosuppression, and may be complicated by progressive heart and nerve amyloid deposition. Importantly, liver transplant does not alter the natural course of central nervous system amyloid disease. To date, no treatment for ATTR penetrates the CNS.

At present there is no FDA approved treatment for ATTR amyloidosis in the US. In Europe, Tafamidis has been approved for treatment of stage 1 ATTR-polyneuropathy since 2012. Tafamidis and Tolcapone bind to the thyroxine binding site of TTR (with different drug-transthyretin interactions) and in so doing stabilizes the tetrameric form of TTR, preventing dissociation and amyloid fibril formation The preclinical and clinical data from a variety of experimental systems support the therapeutic activity of TOLCAPONE in TTR mediated disease.

Detailed Description

This study is designed as a clinical proof-of-concept evaluating whether TOLCAPONE is capable of stabilizing tetrameric TTR (Transthyretin) in the plasma and CSF of symptomatic or asymptomatic patients with leptomeningeal ATTR. Additionally the study will determine the plasma and CSF concentrations of TOLCAPONE needed to induce maximal stabilization of TTR across different TTR variants (TTR mutations).

The study will be carried out in two different populations of subjects, defined by the TTR variant expressed:

* Mutant TTR (up to 10 subjects): symptomatic leptomeningeal TTR patient with any documented leptomeningeal mutations in the TTR gene.

* Mutant TTR (remaining subjects up to 10): asymptomatic leptomeningeal TTR patient with any documented leptomeningeal mutation in the TTR gene.

TTR tetramers stability in plasma and CSF samples will be determined by urea-induced denaturation methodology.

Study Timeline

• Study First Submitted: 2018-07-09
• Study First Submitted QC: 2018-07-09
• Study First Posted: 2018-07-19
• Study Start: 2018-10-30
• Primary Completion: 2019-04-26
• Study Completion: 2019-04-26
• Status Verified: 2019-06
• Last Update Submitted: 2019-06-12
• Last Update Posted: 2019-06-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• Genotyping of variant TTR
• Documented CNS manifestation or expression of variant TTR with leptomeningeal potential

Read More

Exclusion Criteria

• Patients who are unable to provide informed consent
• Contraindication for Tolcapone
• An ALT or AST measurement > 2 times the ULN (Upper Limit of Normal)
• Estimated glomerular filtration rate (eGFR) ≤ 25 ml/min/1.72M2
• Treatment with a known TTR tetramer protein stabilizer within the last 2 weeks

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Tolcapone	Tolcapone	Tolcapone will be administered to assess the short-term (4 weeks) effects on plasma and CSF TTR tetramer stability in subjects with TTR CNS Amyloidosis. Tolcapone is currently licensed for the treatment of Parkinson's disease in combination with levodopa/carbidopa. It is an immediate release product and is currently used at either 100 mg or 200 mg three times a day during waking hours. During this trial, participants will be taking 100mg for 14 days, and then 200mg for 14 days.

Primary Outcome Measures

Name	Time	Method
Change in plasma TTR stabilization	pre-treatment (Day 0) and Day 28	TTR stabilization will be measured in plasma samples from each participant before the first dose of study drug and 2 hours after the last 100 mg study drug dose.
Change in CSF TTR stabilization	pre-treatment (Day 0) and Day 28	TTR stabilization will be measured in CSF samples obtained from each participant before the first dose of study drug and 2 hours after the last 200 mg dose.

Secondary Outcome Measures

Name	Time	Method
Changes in plasma TTR stabilization	Day 14 and Day 28	TTR stabilization will be measured in plasma samples from each participant 2 hours after the day 14 study drug dose.and 2 hours after the 28 day study dose
Tolcapone Concentration in CSF	Day 28	Tolcapone concentration will be measured in CSF at Day 28 2 hours after dose
Tolcapone Concentration in Serum	Day 28	Tolcapone concentration will be measured in serum at Day 28 2 hours after last dose

Trial Locations

Locations (1)

Amyloidosis Center, Boston Medical Center; 🇺🇸 Boston, Massachusetts, United States