Travere Therapeutics @TravereRare
Our mission is to identify, develop and deliver life-changing therapies to people living with rare disease. #InRareForLife https://t.co/uEe4xuJzww travere.com Joined July 2020-
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Today we announced with CSL Vifor that the European Commission has approved FILSPARI (sparsentan) for the treatment of IgA nephropathy (#IgAN). #InRareForLife Press release: bit.ly/3w9cfUc
As we wrap up an excellent few days at #SIMD2024, we are delighted to now be a part of the Genetic Metabolic Dieticians International (GMDI) conference where we’ll continue to share our latest research in the rare metabolic disorder classical #homocystinruia (HCU).
We are here at the @ANNAnurses National Symposium in Orlando, and we are pleased to share some of our latest research on the humanistic burden of #RareKindeyDisease, including #FSGS and #IgAN. Check out all our presentations at ANNA. #InRareForLife
Join us today at #SIMD 2024 for our symposium with Drs. Janet Thomas, Jaya Ganesh, and Wendy Smith. They will speak about unmet need in classical #homocystinuria, recent data from the Phase 1/2 COMPOSE Study, and provide an update of the pivotal Phase 3 HARMONY Study.
Join us tomorrow at @ISNWCN for a CME symposium entitled, Navigating Newer Approaches to Managing IgA Nephropathy, chaired by Siân Griffin, MBBS, Ph.D. The free session, held in-person and virtually, will examine new therapeutic targets for #IgAN. bit.ly/3PCTNK6
We are looking forward to attending #SIMD2024 in NC! We will be presenting 5 posters on our work in classical #homocystinuria, including the trial design of the Phase 3 HARMONY Study of pegtibatinase, an investigational enzyme replacement therapy for the treatment of HCU.
Today we announced that we will present eight abstracts in classical #homocystinuria at @SIMDtweets, April 14-17, 2024, and at #GMDI, April 17-20, 2024 in Charlotte, North Carolina. Read the press release: ir.travere.com/news-releases/… #MetabolicDisease #RareDisease
Today we announced that we will present nine abstracts in rare kidney disease at the World Congress of Nephrology (@ISNWCN) in Buenos Aires, Argentina, on April 13-16, 2024, and the @ANNAnurses National Symposium in Orlando, Florida, on April 14-17, 2024. bit.ly/3U0zLf9…
At @TheACMG #ACMGMtg24 last week in Toronto, we shared our research in classical #homocystinuria. Dr. Can Ficicioglu presented the latest results of the COMPOSE Study evaluating the effect of pegtibatinase, an investigational therapy for people living with classical HCU.
Today we submitted a supplemental New Drug Application (sNDA) to the U.S. FDA seeking full approval of FILSPARI (sparsentan) for the treatment of IgA nephropathy (IgAN). Press Release: bit.ly/49MoN2l
Today, with CSL Vifor, we announced that the European Medicine Agency’s (EMA) CHMP recommends approval of the CMA for sparsentan for the treatment of IgAN. Read the full press release. bit.ly/3wwpzSs
Today Travere reported fourth quarter and full year 2023 financial results. Press release: bit.ly/49i8fyL
Join @GlomCon event on clinical trial updates related to sparsentan in IgA nephropathy Feb. 18 at 8 a.m. PT. Dr. Bruce Hendry will present; panelists include Drs. Shikha Wadhwani and Kirk Campbell, and it will be moderated by Dr. Ali Poyan Mehr. bit.ly/49sNbp1 #Glomcon
At the recent #SSIEM2023 meeting, we presented a satellite symposium on our investigational product in development for classical homocystinuria that is now available online at bit.ly/49DUvPE. #InRareForLife #classicalHomocystinuria #HCU #SSIEM
Join @RPANephrology for a live panel presentation of experts speaking about recently published data on an FDA-approved treatment in IgA nephropathy followed by a panel discussion at 11 a.m. PT on November 17. Register for free here: bit.ly/47dIVJm
Thank you to everyone who joined us at @ASNKidney #ASN23 #KidneyWk and who share our commitment to bringing innovation to people living with #IgAN and #FSGS. We are grateful to all those who contributed to another thought-provoking meeting on advances in #RareKidneyDisease (RKD).
We are committed to bringing life-changing treatments, support, and hope to people living with #RareKidneyDisease (RKD). Learn more about the data we presented at #ASN23 #KidneyWk bit.ly/3SndE1V
Don’t miss our presentations today at @ASNKidney #ASN23 #KidneyWk in Philadelphia. Today we will present 6 of our 11 accepted abstracts. We look forward to seeing you in the exhibit hall.
Today, we presented data from two pivotal head-to-head clinical trials (PROTECT and DUPLEX) at @ASNKidney #ASN23 #KidneyWk, demonstrating our commitment to setting new standards of care to bring hope to people living with #RareKidneyDisease (RKD). bit.ly/3SndE1V
Michelle Rheault @rheault_m
15K Followers 5K Following Ped nephrologist, Division director #NephJC Opinions my own COI: Chinook,Travere,ELOXX, R3R,Aurinia,Otsuka. Alis volat propriis.(she/her) Pronounced “row”
RARE Revolution Magaz.. @RareRevolutionM
12K Followers 8K Following Digital magazine giving a voice to those affected by rare conditions and the charities that support them. Contact us: [email protected]
Beacon for Rare Disea.. @RareBeacon
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Effie Parks @OnceUponAGene
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Int Society of Nephro.. @ISNkidneycare
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GlomCon @GlomCon
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EveryLife Foundation @EveryLifeOrg
7K Followers 3K Following Nonprofit org. dedicated to advancing the development of treatment & diagnostic opportunities for rare disease patients through science-driven public policy.
RARE Revolution Magaz.. @RareRevolutionM
12K Followers 8K Following Digital magazine giving a voice to those affected by rare conditions and the charities that support them. Contact us: [email protected]
Beacon for Rare Disea.. @RareBeacon
12K Followers 11K Following Beacon is a UK-based charity that is building a united rare disease community with patient groups at its heart. Previously known as Findacure.
Int Society of Nephro.. @ISNkidneycare
26K Followers 473 Following International Society of Nephrology #ThisIsISN • World Congress of Nephrology: @ISNWCN • ISN Frontiers Meetings: #ISNFrontiers • Young Nephrologists: #ISNyoung
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KDIGO @goKDIGO
33K Followers 1K Following KDIGO is a global non-profit foundation dedicated to improving the care and outcomes of people with kidney disease worldwide.
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EURORDIS-Rare Disease.. @eurordis
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Nephrology Journal Cl.. @NephJC
36K Followers 1K Following A twice monthly nephrology journal club that meets on Twitter. Hashtag #NephJC
National Kidney Found.. @nkf
44K Followers 909 Following We’re fighting to eliminate preventable kidney disease, accelerate innovation, and dismantle structural inequities in kidney care. Join our fight.
NephCure @nephcure
2K Followers 1K Following Fighting for a world where all who are affected by rare, protein-spilling kidney disease are connected to new and better treatments — and one day, a cure.
Cambridge Rare Diseas.. @camraredisease
8K Followers 7K Following Improving #RareDisease lives. Creators of #RAREfest, #RAREsummit, Companies Forum & #UniqueFeetCam https://t.co/bWJ8DVF9iw
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6K Followers 1K Following A 501(c)(3) nonprofit organization committed to promoting careers, leadership & entrepreneurship for all women in the life sciences. #womeninbio
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2K Followers 4K Following We help clients find rare and non-rare disease patients and caregivers for studies, and connect patients and caregivers with paid research opportunities.
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20K Followers 3K Following National independent nonprofit fighting CKD & ESRD w/prevention, education, clinical research & financial assistance. Take #KidneyAction with @akf_advocacy!
HCU Network America @HCUAmerica
696 Followers 983 Following The mission of HCU Network America is to help patients with #Homocystinuria and related disorders manage their disease and to find a cure. #HCUNetworkAmerica
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SDBNJobs @SDBNJobs
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BiotechStockResearch @BiotechStockRsr
10K Followers 137 Following Independent Research on biotechnology stocks.Announcing our 2024 NORD #RareImpactAwards Industry Innovators! These companies have developed groundbreaking FDA-approved #RareDisease therapies that brought hope to many in our community. Meet the Industry Innovators of 2024: rareimpact.org
Have you read our #NewbornScreening edition yet? This issue has been proudly co-sponsored by @AlexionPharma, @illumina and @TravereRare. Read here: bit.ly/RRNewbornScree… (Link in bio)
We are thrilled to announce that Eric Dube of @TravereRare who has been named in the top 30 of The Medicine Maker's 2023 Power List! Your contributions to the industry have been invaluable, congratulations on this recognition! 🏆 View the list below! fal.cn/3xyJR
Thank you to those who joined our panel discussion addressing barriers within the Cardiovascular and Renal Drugs Advisory Committee. We are grateful to Dr. Jay Wish of @IUMedSchool, Sara Froelich, VP @akebiatx, Jennifer Robinson @SpherixInsights and Lauren Lee @TravereRare.
Great perspectives on the diagnostic odyssey from Catherine Nester, @inozyme, Charlotte Chanson, @orchard_tx, Steve Rodems, @TravereRare, Tom DeFay, @AlexionPharma, Nicole Miller, @ultragenyx, and Walter Kowtoniuk. #GenomicFrontiers23 #raredisease
We're thankful for the support of @TravereRare in our mission of promoting diversity and inclusion for all women in the life sciences. Travere identifies, develops, and delivers life-changing therapies to people living with rare disease. travere.com
Big day ahead! We're kicking off the last day of #RareDC2023 with the Rare Disease Congressional Caucus Briefing "Strengthening the Novel Therapy Dvelopment Ecosystem for Rare Diseases" presented by @TravereRare
The Congressional Caucus Briefing is underway. Sponsor @TravereRare VP William Rote calls Travere’s commitment to the #RareDisease community “personal.”
Thank you to our panel and sponsors for today’s Congressional Caucus Briefing on Strengthening the Novel Therapy Development Ecosystem for #RareDiseases. @ParentProjectMD @EveryLifeOrg @ultragenyx @MilkenInstitute @TravereRare @IGANFoundation #RareDC2023
Thanks to our sponsor, @TravereRare! We would not be successful in our mission of promoting and supporting women in the life sciences without you. @TravereRare identifies, develops, and delivers life-changing therapies to people living with rare disease. travere.com
Start the New Year right by joining AAKP's Building Resilience webinar, designed for kidney patients across the disease spectrum. If you are an early-stage patient, are on dialysis, or have a transplant, you will find these strategies helpful! bit.ly/3XKo5vR @TravereRare
TODAY! Start the New Year right by joining AAKP's Building Resilience webinar, designed for kidney patients across the disease spectrum. If you're an early-stage patient, on dialysis, or have a transplant, you'll find these strategies helpful! bit.ly/3XKo5vR @TravereRare
SOON! Join AAKP's Building Resilience webinar at 3 pm ET, designed for kidney patients across the disease spectrum. If you are an early-stage patient, on dialysis, or have a transplant, you will find these strategies helpful! bit.ly/3XKo5vR @TravereRare @ResilientJJones
Today we welcome @TravereRare to our #OneRareVoice! They join us in our mission to inform policymakers of the unique challenges and promises faced in bringing treatments for #rarediseases to patients.
We're so grateful to @TravereRare for their support in helping expand diversity and inclusion for women in the life sciences. Travere's mission is to identify, develop, and deliver life-changing therapies to people living with rare disease. travere.com
How can you help when a loved one is depressed? This #MentalHealthMonday, download and read the AAKP's pamphlet, "When A Loved One is Depressed: Tips On How You Can Help": bit.ly/3j1Op5W @TravereRare
This #MentalHealthMonday, watch this AAKP HealthLine webinar, "Coping with a Chronic Illness: Sharing the Diagnosis and Finding Support," then share it with those who need it! bit.ly/3F7Syg1 @TravereRare
@TravereRare is returning as a #PASExhibitor. Thank you for being a part of #PAS2023! #pediatricresearch pas-meeting.org/2023-homepage/
It's #MentalHealthMonday! Did you know eating well can positively affect your mental health? Watch this series of AAKP Delicious! recipe videos on our YouTube channel for tasty kidney-friendly recipes ideas and share with those you know! bit.ly/3OLXM5j @TravereRare
Thanks to all who attended our Renal Roundtable last week! Special thanks to Kushal Bhatt, PharmD, MBA and @TravereRare for discussing IgA Nephropathy: Mechanism of Disease with us!
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