Travere Therapeutics

Travere Therapeutics At Travere Therapeutics, we are . travere.com/community-guidelines

09/04/2026

For Jeannie, navigating her daughter Ellie’s classical (HCU) means carefully considering the foods she eats each day.

With Ellie limited to about 9 grams of protein per day, Jeannie shares how their family balances her diet and has learned that even simple choices between fruits and vegetables can make a difference in helping protect Ellie from the harmful effects of protein caused by her classical HCU.

Hear more from Jeannie about the realities of managing a low protein diet for her daughter Ellie.

08/19/2026

Last week, our teams gathered in Chicago for a week of face-to-face collaboration, and the chance to hear firsthand from people navigating life with . Together, these perspectives served as a powerful reminder of why we do what we do and strengthened our commitment to the community.

08/17/2026

Living with often means learning a whole new medical vocabulary.

One common source of confusion is the difference between nephrotic-range proteinuria and nephrotic syndrome.

Think of it this way:
Nephrotic-range proteinuria refers to a high amount of protein leaking into the urine.

Nephrotic syndrome is a group of symptoms and findings that include high protein in the urine, low protein levels in the blood, and swelling caused by fluid buildup.

Knowing the difference can help you better understand FSGS and inform discussions with your healthcare team.

08/14/2026

we’re growing! We recently exceeded more than 500 full-time employees, and when asked what they enjoy most about our company, team members resoundingly say it is our unwavering commitment to our patients and our people.

We’re proud of our work, our team members, and our nonstop focus on people living with rare disease.

08/12/2026

Protein in your urine is never something to ignore.

Known as proteinuria, it can be one of the earliest signs that your kidneys aren't working as they should. A simple urine test can detect proteinuria and help start an important conversation with a healthcare provider about what's causing it.

In this video, David Rush, who was diagnosed as a teenager with a called , shares why knowing about protein in your urine is critical.

What a joy it was to be at the IgA Nephropathy Foundation’s in Atlanta. Seeing new and old friends, and hearing from g...
08/05/2026

What a joy it was to be at the IgA Nephropathy Foundation’s in Atlanta. Seeing new and old friends, and hearing from glomerular disease experts talk about all the recent developments in care is a reminder of how much progress has happened in . We are proud to support the work of the foundation to ensure people with IgA nephropathy do not feel alone.

07/31/2026

Before she was born, Gabbi’s classical journey had already begun. Diagnosed through amniocentesis, early detection gave her parents the opportunity to start managing her from the very beginning.

Gabbi learned the importance of understanding her condition, speaking up for her needs, and becoming her own advocate early on, whether at the doctor’s office, in the classroom, or with friends. Today, she partners with Homocystinuria - HCU Network America and uses her voice to advocate for herself and others living with rare disease.

Learn more about Gabbi’s drive and passion for rare disease advocacy in her Rare Life story. https://travere.com/rare-life/gabbi/

Newborn screening is one of the most effective public health programs in the U.S. It gives babies the chance for early d...
07/29/2026

Newborn screening is one of the most effective public health programs in the U.S. It gives babies the chance for early diagnosis and treatment and can change the trajectory of thousands of lives each year. But across the country, states are working with increasingly limited resources and delays which result in preventable death and disability. Adding new approved conditions can take up to 10 years or more for federally approved conditions to be fully adopted by states. In the meantime, babies are missed.

That is why the Surge to Save Newborns campaign was born.

This effort is focused on a straightforward goal: dedicated funding for newborn screening so every baby, in every state, is screened for every recommended condition. Learn more at https://surgetosave.org.

We were proud to join NephCure’s Rare Kidneys on the Hill Day, standing alongside patients, healthcare professionals, re...
07/24/2026

We were proud to join NephCure’s Rare Kidneys on the Hill Day, standing alongside patients, healthcare professionals, researchers, and advocates to help elevate the voices of the community on Capitol Hill.

Continued advocacy is essential to advancing policies that support people living with , including the New Era for Preventing End Stage Kidney Disease Act. Thank you to everyone who shared their stories and advocated for meaningful policy change. Together, we can bring hope to the RKD community.

Address

3611 Valley Centre Drive, Suite 300
San Diego, CA
92130

Opening Hours

Monday 8am - 5pm
Tuesday 8am - 5pm
Wednesday 8am - 5pm
Thursday 8am - 5pm
Friday 8am - 5pm

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+18889697879

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