The kidneys are like your body's natural filtration system. They clean your blood, remove waste, and help to maintain the right balance of fluid and minerals. When a person has healthy kidneys, little to no protein is found in the urine. When kidneys aren’t working properly, protein that should stay in the blood spills from the kidneys into the urine. Had you heard these terms before diagnosis? We are focused on supporting the kidney community, helping people understand their diagnosis and navigate disease progression. https://lnkd.in/g2e7TC-a
Travere Therapeutics
Biotechnology
San Diego, California 42,958 followers
In rare for life.
About us
Our mission is to identify, develop and deliver life-changing therapies to people living with rare disease. #InRareForLife Community Guidelines: https://travere.com/community-guidelines/
- Website
-
https://www.travere.com
External link for Travere Therapeutics
- Industry
- Biotechnology
- Company size
- 201-500 employees
- Headquarters
- San Diego, California
- Type
- Public Company
- Founded
- 2020
Locations
-
Primary
Get directions
3611 Valley Centre Dr
Suite 300
San Diego, California 92130, US
-
Get directions
3 Dublin Landings
North Wall Quay
Dublin 1, IE
-
Get directions
Zürcherstrasse 6
CH-8640 Rapperswil-Jona, CH
Employees at Travere Therapeutics
Updates
-
Today on World Homocystinurias Awareness Day, we recognize all those living with this metabolic condition. Classical #homocystinuria, the most common form of homocystinuria, is a rare genetic metabolic disorder in which the body cannot properly process the amino acid methionine, a building block of protein. Gabbi, who lives with classical HCU, talks about how she first came to understand her diagnosis when her dad used LEGO bricks to explain protein and how it is metabolized. Watch how her dad’s “LEGO talk” gave Gabbi the confidence to share her diagnosis with others. #InRareForLife #worldhomocystinuriasawarenessday #WHAD2026 #HCUawareness
-
On Homocystinurias Awareness Day, we recognize the significant unmet need facing people living with classical #homocystinuria and the families navigating this complex disease every day. As Eric Dube shares in this article, we remain focused on advancing work that we hope can meaningfully improve outcomes for people living with this rare disease. #HCUawareness #InRareForLife
-
We have arrived to Rio Grande, Puerto Rico, for the 2026 Society for Inherited Metabolic Disorders annual meeting. Our metabolic team looks forward to sharing our patient-reported outcomes research from the ACAPPELLA Study, a natural history study examining the physical and mental health impacts of classical #homocystinuria (HCU). We will also highlight the study designs of our Phase 3 HARMONY and ENSEMBLE clinical trials evaluating pegtibatinase as a potential novel treatment for classical HCU. #InRareForLife
-
-
Today is IgA Nephropathy Awareness Day and the birthday of a very special organization dedicated to people living with #IgAN. Cheers to The IgA Nephropathy Foundation and all you’ve done to help the global IgAN community. You have touched so many lives, and we’re proud to support your work raising awareness and bringing hope to people with this #RareKidneyDisease. #IgANDay #InRareForLife
-
-
As the treatment landscape in IgA nephropathy continues to evolve, variability in care remains. In this article, Jula reflects on work presented at NKF Spring Clinical Meeting and how implementation science can help address real-world barriers. #InRareForLife #IgANDay
-
Great food, captivating conversation, and even better moments #HereAtTravere! Earlier this week, local team members came together for a food truck lunch and enjoyed delicious bites and sweet treats. At Travere, we value our team members and the quality time we share when we come together at our San Diego office. #InRareForLife
-
-
Jeff and his family, like others who have faced the diagnosis of a #RareKidneyDisease, were surprised to learn that he had #IgAnephropathy. This 12-minute Medical Stories segment aired via the PBS stations when it was released. The story includes expert commentary from Jai Radhakrishnan, M.D., Columbia University Medical Center. Interviews with Jeff and his wife (and care partner) Joy share an intimate look into their day-to-day lives, and how they are each impacted by Jeff’s IgA nephropathy, while Dr. Radhakrishnan explains the disease and the urgency to protect kidney function in IgAN. As we approach #IgANDay, check out Jeff’s story. #InRareForLife https://bit.ly/3R48c5A
Medical Stories - Rare Kidney Disease: Jeff's Story
https://www.youtube.com/
-
We are delighted to be sharing new #RareKidneyDisease data at #NKFClinicals National Kidney Foundation. Don’t miss our poster presentations Thursday, May 7, 5:15 to 7:30 p.m. ET on proteinuria reduction in #IgAN and #FSGS.
-
Today we reported our first quarter 2026 financial results and provided a corporate update. Press Release: https://bit.ly/4tdvN0U
-