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TTR stabiliser

Tafamidis (Vyndaqel, Vyndamax)

Transthyretin normally travels as four pieces held together. When they come apart, they clump into amyloid in the heart. Tafamidis holds the pieces together, and it works whether the problem came from your genes or from age.

Chemical structure of Tafamidis (Vyndaqel, Vyndamax): tafamidis, drawn by MyGeneLog™ from PubChem records
Chemical structure of tafamidis, drawn by MyGeneLog™ from public PubChem records. Free to reuse under CC BY 4.0 with credit to MyGeneLog™.

What this drug connects to

Tafamidis (Vyndaqel, Vyndamax) Condition: Transthyretin Amyloidosis (ATTR) Transthyretin Amyloidosis (ATTR) Condition Variant: rs1791209 · TTR rs1791209 · TTR Variant Variant: rs28933981 · TTR rs28933981 · TTR Variant Variant: rs528071310 · TTR rs528071310 · TTR Variant Variant: rs76992529 · TTR rs76992529 · TTR Variant Tafamidis (Vyndaqel, Vyndamax) Tafamidis (Vyndaqel, Vyndamax) TTR stabilis…

The genes involved

TTR

Transthyretin Amyloidosis (ATTR) →

Tafamidis (Vyndaqel, Vyndamax) is a stabiliser: it holds the four pieces of transthyretin together so they cannot fall apart and turn into amyloid. It is a pill taken once a day, approved in the US since 2019 for the heart form of ATTR, whether hereditary or wild-type, so your genotype does not decide whether you can take it. In its main trial of 441 patients over 30 months, fewer people died or were admitted to hospital for their heart than on placebo. Whether to take it is decided with a specialist, and nothing here is a reason to start, stop or change a medicine.

ATTR-ACT (Maurer MS et al., NEJM 2018, PMID 30145929); VYNDAQEL/VYNDAMAX US prescribing information (DailyMed).

Variants MyGeneLog™ reports for these genes

These are the positions in your own file that carry the genes above. Not every gene in a guideline is one we report — where that is the case the gene appears above without a variant here, and the note says so.

Retinol-binding protein 4 levels

TTR · rs1791209

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TTR protein levels

TTR · rs28933981

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MEP1B protein levels

TTR · rs528071310

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Metabolite peak levels (QI722)

TTR · rs76992529

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Questions about Tafamidis (Vyndaqel, Vyndamax)

What is tafamidis?

Tafamidis, sold as Vyndaqel and Vyndamax, is a daily pill for the heart form of transthyretin amyloidosis (ATTR). It holds the four pieces of transthyretin together so they cannot fall apart and build up in the heart.

Do I need a TTR gene variant to take tafamidis?

No. Its US label covers the heart form of ATTR whether it is hereditary or wild-type, the kind that comes with age. A genetic test still matters, because a variant means your relatives can be tested.

How well does tafamidis work?

In its main trial, 441 patients were followed for 30 months. Fewer people on tafamidis died or were admitted to hospital for their heart than on placebo. Whether to take it is decided with a specialist; nothing here is a reason to start, stop or change a medicine.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Tafamidis (Vyndaqel, Vyndamax). MyGeneLog™. https://www.mygenelog.com/drugs/tafamidis

This page is educational and contains no dosing information. Where a clinical guideline covers one of these gene-drug pairs it is written for prescribers and works through validated algorithms alongside clinical monitoring. Nothing here is a reason to start, stop, or change a medication — that conversation belongs with the clinician or pharmacist managing your treatment.