Global campaign for equitable access to all Vertex CFTR modulator drugs which can extend & save the lives of people with cystic fibrosis (CF) wherever they live

Joined October 2020
🚨@VertexPharma charges $370,000 a year for a drug that keeps people with cystic fibrosis (CF) alive - pricing it out of reach for most. So CF families built their own access: Triko, is the same medicine but 95% cheaper ⬇️
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🚨 BREAKING: Yesterday at #NACFC we announced the first truly affordable #cysticfibrosis modulator is here. The CF community is reviving the CF Buyers’ Club with Triko: - A generic version of Trikafta - Costs just $6,375 per child/yr 🔗 To find out more: cfbuyersclub.org
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Vertex Save Us retweeted
Una simple pastilla cambiaría la realidad de al menos 8 000000 de mexicanos y sus familias @Claudiashein @SSalud_mx @Tu_IMSS @VertexSaveUs @SSalud_mx – at Venustiano Carranza, Distrito Federal
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💥Historic news today!💥 #Trikafta (ETI) is the first CF treatment to be added to the @WHO ‘Essential Medicines List’. We’ve worked tirelessly with academics & allies to make this possible. This listing must translate into access for all. Govt’s & @VertexPharma must step up.
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Vertex Save Us retweeted
So many years of work behind today's decision #Trikafta is on the @WHO Essential Medicines List! Well done @VertexSaveUs @JustTreatment & all the advocates/medical professionals worldwide who contributed to this ground breaking achievement Now @VertexPharma - DROP YOUR PRICES
🚨 BREAKING: @WHO adds #Trikafta to its Essential Medicines List – the first cystic fibrosis medicine ever included. This recognises what families have said all along: CF medicine is essential & lifesaving. Now @VertexPharma must drop patents, drop the price & deliver access.
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Vertex Save Us retweeted
Huge news today that Trikafta (ETI) is now on the @WHO ‘Essential Medicines List’. The first ever CF drug to be listed💥 So proud to be part of a group of academics/advocates that worked on the submission 🥰 @VertexPharma & govt’s must act now. Trikafta for all! #EML 👊💊🌎🫁
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Great to be mentioned in this paper about access to CF modulators in Brazil, following our involvement there in 2022/3. We know threatening Vertex’s monopoly with compulsory licensing is the ONLY language they respond to = lower pricing. Read more: righttobreathe.net/post/cyst… 🇧🇷
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This is what keeps me up at night. How can there be miracle drug for those of us born with CF, yet the barrier to get it is $30,000 per month?!?! UNCONSCIONABLE
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South African #cysticfibrosis patient JC speaks about about @VertexPharma’s inhumane & inequitable ‘access programme’ that means that only the privileged can access Trikafta, while he & the other 50% are left behind. The @CompComSA must re-open their investigation now. 😡
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Today we’ve been @CompComSA to deliver a dossier of evidence showing that @VertexPharma has misled them & that 50% of CF patients in SA are still dying w/o access to #Trikafta. They must reopen their investigation into Vertex’s anti-competitive behaviour. No one left behind!
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🚨 BREAKING: #CysticFibrosis families handed over a 100-page dossier to @CompComSA. It shows how @VertexPharma misled the Commission & public. Half of CF patients still can’t access lifesaving #Trikafta. We demand the investigation be re-opened. #NoOneLeftBehind @VertexSaveUs
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Dear Vertex-You are truly vile. How dare u raise prices on a life saving drug that none of us can afford? WHO has an extra $30,000 per month?!?! Signed-a CF WARRIOR
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Nothing surprises us when it comes to the greed & inhumane behaviour of @VertexPharma. Children are dying w/o access to #Trikafta due to the unaffordable price. Vertex’s response - to INCREASE the price. That says everything about their utter disregard for CF patients 🤬
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Amazing news from #Turkey today - CF patients aged 6+ will have access to #Trikafta. ❤️ BUT… Why did it take 6 years whilst @VertexPharma blocked efforts to access affordable alternatives? How many young lives were lost? 😞 And 000’s globally are still waiting 😡 #CFCantWait
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A huge thank you to everyone that came & showed their support by placing a rose at the @VertexPharma stand at the European CF Conference in memory of CF children that have died without access to #Trikafta 💔 The global CF family standing together is an incredible thing ❤️🌎💊👊
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🚨 BREAKING: today #cysticfibrosis mums stage a powerful intervention at @VertexPharma’s stand. Gayle 🇬🇧, Urtė 🇱🇹 & Ajsela 🇦🇱 laid a wreath for children who died waiting for #Trikafta. Backed by clinicians, we demand @VertexPharma act now, access for all! #ECFC2025
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Vertex Save Us retweeted
Replying to @VertexPharma
@VertexPharma hiding from the truth! #Cysticfibrosis
Our representatives were blocked from entering a ‘CF community’ meeting at the European CF Conference in Milan by @VertexPharma. Inexcusable & indefensible. #Trikafta4All #RightToBreathe
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