On air · 3 of 3 networks
BridgeBio
- bridgebio.com
- Healthcare & Life Sciences
- US
- 1,098 employees
BridgeBio’s ads on LinkedIn, Meta and Google, recorded by adsrunning. Browse the latest here for free. Sign up free to see all 219. Watch BridgeBio with Starter to get each new one in your feed.
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| Network | Status | Live ads | Nov 2025LinkedIn activity · 52 weeksOct 2026 | Checked | Next step |
|---|---|---|---|---|---|
| Running | 219 | Checked 30 Oct 2026 | See all 219 ads → | ||
| Meta | Running | 25 | Active ads on the Meta Ad Library, all countries | Checked 27 Oct 2026 | Collect them with the API → |
| Running | 100+ | Ads on the Google Ads Transparency Center | Checked 24 Oct 2026 | Collect them with the API → |
BridgeBio has 219 live LinkedIn ads. Its Facebook page had 25 active ads on 27 Oct 2026, and we recorded 100+ Google ads on 24 Oct 2026.
Latest ads
- LINKEDIN · VIDEORecorded 11 Sept 2026
We’re excited to introduce new updates to MyAchonJourney! This one-stop educational resource, developed in collaboration with advocacy leaders and healthcare experts, now includes guidance for two new age groups: • Middle childhood (ages 6-12) • Teenage years (ages 13-17) These additions build on existing resources for early childhood, ensuring families have access to reliable information at every stage of their journey. Explore the latest updates here: myachonjourney.com
- LINKEDIN · CAROUSELRecorded 8 Oct 2026
Learn the importance of genetic testing for LGMD2I/R9 to help accelerate time to a diagnosis for your patients.
- LINKEDIN · CAROUSELRecorded 8 Oct 2026
In LGMD2I/R9, diverse symptoms and variable onset can delay a diagnosis.
- LINKEDIN · CAROUSELRecorded 8 Oct 2026
Understand the symptoms of LGMD2I/R9 to help patients receive a diagnosis. LGMD2I/R9 now has a specific ICD-10 code.
- LINKEDIN · IMAGERecorded 11 Sept 2026
ADH1 can be difficult to diagnose based on symptoms alone and patients often face a prolonged delay before receiving a final diagnosis.
- LINKEDIN · IMAGERecorded 11 Sept 2026
Genetic testing can establish the root cause of a patient’s symptoms, like ADH1 due to an inherited variant CASR.
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