Alyftrek

Vanzacaftor, tezacaftor, and deutivacaftor · Vertex Pharmaceuticals Incorporated
PRESCRIPTION ONLY (USA)

Alyftrek ingredients

Active ingredientStrength
Vanzacaftor4 mg/1, 10 mg/1
Tezacaftor20 mg/1, 50 mg/1
Deutivacaftor50 mg/1, 125 mg/1

What Alyftrek is used for

The FDA lists the approved uses on the official label (below). In the EU, ivacaftor;tezacaftor;elexacaftor is approved as Kaftrio for:

Kaftrio tablets are indicated in a combination regimen with ivacaftor for the treatment of cystic fibrosis (CF) in patients aged 6 years and older who have at least one non-Class I mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Kaftrio granules are indicated in a combination regimen with ivacaftor for the treatment of cystic fibrosis (CF) in paediatric patients aged 2 to less than 6 years who have at least one non-Class I mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

EU wording from the European Medicines Agency; US approved uses can differ.

Key facts

Brand
Alyftrek
Generic name
Vanzacaftor, tezacaftor, and deutivacaftor
Made by
Vertex Pharmaceuticals Incorporated
Forms
Tablet, Film Coated
Given
Oral
Drug class
Cystic Fibrosis Transmembrane Conductance Regulator Potentiator
FDA approval
New drug application (NDA) NDA218730
On the US market since
2024

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Alyftrek?

Alyftrek (Vanzacaftor, tezacaftor, and deutivacaftor) is a specialist medicine made by Vertex Pharmaceuticals Incorporated, approved by the US FDA.

What are the ingredients of Alyftrek?

Alyftrek contains Vanzacaftor (4 mg/1, 10 mg/1); Tezacaftor (20 mg/1, 50 mg/1); Deutivacaftor (50 mg/1, 125 mg/1).

Is Alyftrek approved in Europe?

The same active substance is approved in the EU as Kaftrio, Alyftrek, Symkevi.

From the FDA National Drug Code directory (open.fda.gov, public domain) and the European Medicines Agency medicines list. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, USA

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.