In research,
we go
further
together
We’re exploring an investigational treatment for ATTR amyloidosis, where you’re not just part of the study— YOU help lead the way
Introducing the TRITON‑PN study
TRITON-PN is a clinical research study for individuals who have hereditary ATTR amyloidosis with polyneuropathy.
TRITON-PN is a phase 3 study to:
The TRITON-PN team will give study participants either nucresiran or vutrisiran, an approved medication for the treatment of amyloidosis. They want to see how nucresiran works when compared to vutrisiran. They also want to see how nucresiran works when compared to a placebo (a placebo is a substance that looks like the investigational medication but has no active ingredients).
There is no placebo in this study. Doctors will look at how participants respond to nucresiran and compare it to a group that received placebo in an earlier study.
What is the purpose
of this study?
This study is being done to find out if nucresiran can affect nerve health and reduce the symptoms of neuropathy in people with hereditary ATTR amyloidosis with polyneuropathy.
Researchers also want to see how nucresiran affects the quality of life of people living with this condition.
Can I be in the
TRITON-PN study?
You could be eligible for this study if you:
- Are 18 to 85 years old
- Have hereditary ATTR amyloidosis (confirmed through genetic testing) with polyneuropathy
Study timeline
Screening Period
Up to 45 days
- Assessments and procedures to see if you can be in the study
Treatment Period
18 months
- Assessments and procedures to learn about nucresiran
- Study visits every 3 months (a few visits will happen more often)
Treatment Extension Period
Up to 18 months
- Assessments and procedures to learn about nucresiran
- Study visits will vary every 3 to 6 months
Follow-up Period
Up to 12 months
(24 months for individuals who are able to become pregnant)
- Assessments and procedures to monitor your health after you finish taking nucresiran
- Study visits every 6 months
What to expect in TRITON-PN
The TRITON-PN study
happens in 4 parts.
- In the Screening Period, we'll determine if you're eligible for the study
- In the Treatment Period, you'll receive either nucresiran or vutrisiran. You'll have a 4 out of 5 chance of receiving nucresiran, and a 1 out of 5 chance of receiving vutrisiran
- In the Treatment Extension Period, you'll receive nucresiran
- In the Follow-up Period, our study team will keep an eye on your health
The study doctor will:
Perform neurological exams
Check your vital signs
(your blood pressure, heart rate, breathing rate, and temperature)
Perform physical exams
Take blood and urine samples
Measure the electrical activity of your heart
(electrocardiogram)
Check your vital signs
(your blood pressure, heart rate, breathing rate, and temperature)
Ask you to complete questionnaires