
We move at the speed of patient need. We exist to bring meaningful medicines to people living with genetic conditions. $BBIO
Palo Alto, California
Joined January 2021
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We will report Q3 2026 financial results and a business update after market close Thurs, Oct 29. Conference call at 4:30pm ET same day. Details: bit.ly/488BVPY
"A major problem for rare disease research is funding." – Guangping Gao, M.D., UMass Chan Medical School. Noa is one of more than 30 million Americans living with a rare disease. Behind that number are families still waiting. Watch the full video on our Insights page: bit.ly/4z9U5fL
Allelic series: the human genetics evidence that helps you pick the right drug target. About 1 in 10 drugs that reach clinical testing are approved, and most failures are good molecules aimed at the wrong target. Try our new interactive feature: bit.ly/4z03fMg
Heart failure science, live in Phoenix. 🫀
We recently attended the @HFSA (#HFSA2026) Annual Scientific Meeting in Phoenix.
Conferences like this are where the heart failure community comes together to share new data, trade ideas, and keep the focus on patients. We were glad to be there listening, learning, and connecting with clinicians, researchers, and advocates working to improve outcomes.
Thank you to everyone who stopped by to say hello. We enjoyed hearing what’s on your mind and look forward to continuing the conversation on ATTR-CM.
That’s a wrap on #ASBMR2026. We shared Phase 3 CALIBRATE data on investigational encaleret in ADH1, family genetic testing findings with the HypoPARAthyroidism Association, and infigratinib research in achondroplasia. Thank you to the investigators, participants and families.

ALT A group of people is gathered in front of a BridgeBio Medical booth at an event. They are standing and smiling at the camera. Several kiosks with monitors displaying colorful graphics are visible. The booth features text and branding related to BridgeBio.

ALT A group of six people smiling together in an exhibition booth. The booth displays signs for "BridgeBio," a company name visible in the background. The setting appears professional with informational text about advancing care for people living with ADH. The individuals have conference badges around their necks.
For people living with chronic #hypopara and their caregivers, learning about a #clinicaltrial begins with clear, accessible information. Take a closer look at what researchers hope to learn through the RECLAIM-HP Study and how the study medicine is given.
“The first thing that pops up is that life expectancy is about ten. That was when we realized how bad it really was.” – Lori Greenwood, Noa's mother. Noa is one of more than 30 million Americans living with a rare disease. Behind that number are families still waiting. Watch the full video on our Insights page: bit.ly/4z9U5fL
Those living with limb-girdle muscular dystrophy (LGMD) often prioritize maintaining their day-to-day functioning. Learn the possible signs of LGMD and how recognizing them could lead to earlier diagnosis.
At #HFSA2026 in Phoenix, BridgeBio and independent investigators shared new real-world evidence and Phase 3 analyses in ATTR-CM. We're grateful to the investigators, clinicians and, above all, the patients and families whose participation makes this research possible. Learn more: bit.ly/4hVEVnn
Today at #ASBMR2026, we presented new bone turnover and participant-reported outcome data from the Phase 3 CALIBRATE trial of investigational encaleret in ADH1. We also dosed the first participant in RECLAIM-HP, our Phase 3 study of encaleret in chronic hypoparathyroidism. Learn more: bit.ly/4zjQls3
Thank you, #NMSG2026! The smaller setting gave us time for detailed conversations with the neuromuscular community about our Phase 3 FORTIFY study in LGMD2I/R9. Your partnership moves this work forward.
That's a wrap on #WMS2026! We had a full room at our symposium and great talks with clinicians, researchers and advocates from the U.S. and Japan. Thank you to everyone who joined us. We're grateful for this community and the partnerships moving LGMD care forward.
This #DwarfismAwarenessMonth, hear from Gwyn, host of A Little View, about growing up with #achondroplasia, body image, and finding strength in community on the #OnRarePodcast. "You're still a person; you still have feelings." 🎧 bit.ly/47M9tTK
We’re proud to share that Christine Zhang, Executive Director, Evanesco Program Lead at BridgeBio, has been named to this year’s BioSpace’s 40 Under 40 cohort.
Christine’s leadership embodies the innovative thinking and scientific conviction that drives our mission to deliver transformative medicines where they are needed most.
Congratulations, Christine!
Read more: bit.ly/4ARlN2C
The FDA has accepted our NDA for infigratinib in achondroplasia. PDUFA date: February 4, 2027. If approved, it would be the first oral therapy for children with achondroplasia. $BBIO
bit.ly/4diXyAm
Heading to #ASBMR2026 in Boston! We'll present participant-reported outcomes and bone data from our Phase 3 CALIBRATE trial of encaleret in #ADH1, plus new genetic testing data. Details: bit.ly/47F7cK4
We will be at #HFSA2026 in Phoenix, Oct 9–12. At @hfsa, we will share updates in ATTR-CM, including an independent comparative real-world analysis using Epic Cosmos EHR data.
Full schedule: bit.ly/3Ty5s23
Muscle weakness has a long list of possible causes. Genetic testing is what names the one you have. Neha Gandhi of BridgeBio Neuromuscular and Kelly Brazzo of CureLGMD2i went Behind the Mystery on @lifetimetv on #LGMD diagnosis, advocacy and community. Watch the replay: bit.ly/4hlitVF
For people living with chronic #hypoparathyroidism—and the families and care teams who support them—learning about a #ClinicalTrial may begin with questions. Swipe through for an introduction to the RECLAIM-HP Study, what researchers hope to learn, and where to find more information.
















