Deupirfenidone compared with pirfenidone and placebo in idiopathic pulmonary fibrosis (ELEVATE-IPF): a phase 2b randomized placebo-controlled trial
Deupirfenidone slowed the rate of FVC decline compared with placebo in IPF
https://t.co/Bqk4xHlIym
@TobyMMaher@atscommunity
The first snRNASeq & spatial transcriptomic analysis of bronchoscopic cryobiopsies from patients with Early IPF & preserved pulmonary functions is out on @biorxivpreprint and message is Early IPF is IPF‼️
https://t.co/yyX28bn7D2
Shoutout to @drcastelino, @tobymmaher, and Dr. Flaherty for leading an amazing discussion at #CHEST2025! Real-world takeaways for real-world care.
📺 Replay available here: https://t.co/kVyouNbpvq
Thanks to @Boehringer for their educational grant support #CME#MedEd
Watch Toby Maher, MD, MSc, PhD (@TobyMMaher), Flavia Castelino, MD (@drcastelino), and Kevin R. Flaherty, MD, MS discuss clearing the air on fibrosing ILDs at #CHEST2025 – to participate, visit: https://t.co/kVyouNbXkY https://t.co/aT4XRrm95f
Yesterday, the U.S. FDA approved Jascayd (nerandomilast) to treat IPF. This is the first IPF new therapy approved in more than a decade.
Congratulations to all our patients & yes, even better drugs are on the way!!
Great day for #CureIPF#ScienceMatters
https://t.co/edUy8DqUUJ
⚡ Up your #fibrosingILD game! Join @PeerView + the experts Drs. Toby Maher (@tobymmaher) & Castelino (@drcastelino) at #CHEST2025 (Oct 21 | 6 AM CDT) for a rapid-fire TownHall on antifibrotics, immunomodulators & emerging therapies. 🫁
👉 https://t.co/icSA9ezpvE #MedEd
What do most clinicians miss about idiopathic pulmonary fibrosis?
Find out in the latest episode, where @doctor_saranya speaks with @TobyMMaher about what defines Interstitial Lung Disease, how idiopathic pulmonary fibrosis fits into the picture and more: https://t.co/a9VZFYyQ0t
Fantastic news for all our patients with IPF who suffer with cough! An overall 43% reduction in cough counts, similar improvement in patient reported cough and benefits seen in 2 weeks. We look forward to the phase 3 study!
When it rains it pours!! What an amazing #ATS2025 for #CurePF4ALL! Nerandomilast -> ⬇️FVC decline compared to placebo in Progressive Pulmonary Fibrosis patients on antifibrotics or untreated. 👏🏼 Drs Maher, Martinez & #FibroneerILD team!!
https://t.co/qhAmNZalCk
Wow! What a day for #CureIPF & #ATS2025! First positive drug trial in 10 years in IPF!! Treatment with Nerandomilast -> ⬇️FVC decline compared to placebo in patients on antifibrotics or untreated. Kudos Drs Richeldi and Wijsenbeek and #FibroneerIPF team https://t.co/ZRw5qwTlPc
Great to see publication of the first positive phase 3 trial in patients with IPF. This represents an important step forward in the treatment of this terrible disease. #cureipf
Presented at #ATS2025:
In the FIBRONEER-IPF phase 3 trial, nerandomilast slowed disease progression in patients with idiopathic pulmonary fibrosis as compared with placebo. Full trial results: https://t.co/gjXxPWFpyR
@atscommunity
A reminder to tune in to our session at #ATS2025 on cough in pulmonary fibrosis. Join @TobyMMaher to discuss how new technologies and patient-reported outcomes can address this gap in IPF research.
Add to your calendar and join us! https://t.co/4XvCPMtIMC
#IPF#digitalhealth
Join Strados Labs and @TobyMMaher at #ATS2025 for an engaging session on the often-overlooked symptom of cough in pulmonary fibrosis and ways we can address the gap.
May 19, 11:55 AM PST | Exhibitor Hall Innovation Hub #7
We look forward to seeing you there! #IPF
Predicting Failure: Can Blood Biomarkers Identify Likely Treatment Non-Responders in IPF?
https://t.co/VD6dDe8OxZ
and Editorial by Toby Maher @tobymmaher on recent research:
https://t.co/2WhY0a0mY6
Follow us on Bluesky: @respirology.bsky.social
Fibrosis: cross-organ biology and pathways to development of innovative drugs https://t.co/FY8SCQgvg2
This new Review highlights core pathways active in fibrotic conditions across organs, and proposes strategies to improve the translation of potential antifibrotic drugs