Vera Therapeutics Announces Late-Breaking Oral Presentation of ORIGIN Phase 2b Long-term Results at the American Society of Nephrology Kidney Week 2024
Vera Therapeutics (Nasdaq: VERA) announced that long-term results from the ORIGIN Phase 2b clinical trial of atacicept for IgAN treatment will be presented at the American Society of Nephrology (ASN) Kidney Week 2024 in San Diego, from October 23 to 27. The presentation will be delivered by Dr. Jonathan Barratt on October 26. Additionally, two informational posters describing the ORIGIN Phase 3 and ORIGIN Extend trials will be presented by Dr. Richard Lafayette on October 25.
Vera will also host an in-person and virtual R&D Day in New York on October 2, 2024, featuring experts Dr. Jonathan Barratt, Dr. Richard Lafayette, and Dr. Brad Rovin, who will discuss Vera's expanded atacicept R&D activities.
Vera Therapeutics (Nasdaq: VERA) ha annunciato che i risultati a lungo termine del trial clinico ORIGIN Fase 2b riguardante il trattamento dell'IgAN saranno presentati alla Settimana dei Reni 2024 dell'American Society of Nephrology (ASN) a San Diego, dal 23 al 27 ottobre. La presentazione sarà tenuta dal Dr. Jonathan Barratt il 26 ottobre. Inoltre, due poster informativi che descrivono i trial ORIGIN Fase 3 e ORIGIN Extend saranno presentati dal Dr. Richard Lafayette il 25 ottobre.
Vera ospiterà anche un Giorno R&D in presenza e virtuale a New York il 2 ottobre 2024, con la partecipazione degli esperti Dr. Jonathan Barratt, Dr. Richard Lafayette e Dr. Brad Rovin, che discuteranno delle attività di R&D ampliate di atacicept di Vera.
Vera Therapeutics (Nasdaq: VERA) anunció que los resultados a largo plazo del ensayo clínico ORIGIN Fase 2b sobre el tratamiento de IgAN se presentarán en la Semana de los Riñones 2024 de la American Society of Nephrology (ASN) en San Diego, del 23 al 27 de octubre. La presentación será realizada por el Dr. Jonathan Barratt el 26 de octubre. Además, dos carteles informativos que describen los ensayos ORIGIN Fase 3 y ORIGIN Extend serán presentados por el Dr. Richard Lafayette el 25 de octubre.
Vera también organizará un Día de I+D presencial y virtual en Nueva York el 2 de octubre de 2024, con la participación de expertos como el Dr. Jonathan Barratt, el Dr. Richard Lafayette y el Dr. Brad Rovin, quienes discutirán las actividades ampliadas de I+D sobre atacicept de Vera.
베라 테라퓨틱스(Vera Therapeutics, Nasdaq: VERA)는 IgAN 치료를 위한 아타시셉트(atacicept)의 ORIGIN 2b 임상 시험의 장기 결과가 2024년 10월 23일부터 27일까지 샌디에이고에서 열리는 미국 신장학회(ASN) 신장 주간에서 발표될 것이라고 발표했습니다. 발표는 10월 26일에 조나단 바렛 박사(Dr. Jonathan Barratt)에 의해 진행됩니다. 또한, ORIGIN 3 기 및 ORIGIN Extend 시험을 설명하는 두 개의 정보 포스터가 10월 25일에 리차드 라파예 박사(Dr. Richard Lafayette)에 의해 발표될 것입니다.
베라는 또한 2024년 10월 2일 뉴욕에서 대면 및 가상 R&D 데이를 개최하며, 조나단 바렛 박사, 리차드 라파예 박사, 브래드 로빈 박사와 함께 베라의 아타시셉트 R&D 활동 확장에 대해 논의할 예정입니다.
Vera Therapeutics (Nasdaq: VERA) a annoncé que les résultats à long terme de l'essai clinique ORIGIN Phase 2b d'atacicept pour le traitement de l'IgAN seront présentés lors de la Kidney Week 2024 de l'American Society of Nephrology (ASN) à San Diego, du 23 au 27 octobre. La présentation sera faite par le Dr. Jonathan Barratt le 26 octobre. De plus, deux affiches informatives décrivant les essais ORIGIN Phase 3 et ORIGIN Extend seront présentées par le Dr. Richard Lafayette le 25 octobre.
Vera organisera également une journée R&D en présentiel et virtuelle à New York le 2 octobre 2024, avec la participation d'experts tels que le Dr. Jonathan Barratt, le Dr. Richard Lafayette et le Dr. Brad Rovin, qui discuteront des activités R&D étendues d'atacicept de Vera.
Vera Therapeutics (Nasdaq: VERA) gab bekannt, dass die Langzeitresultate der ORIGIN Phase 2b klinischen Studie zu Atacicept zur Behandlung von IgAN auf der American Society of Nephrology (ASN) Kidney Week 2024 in San Diego vom 23. bis 27. Oktober präsentiert werden. Die Präsentation wird am 26. Oktober von Dr. Jonathan Barratt gehalten. Darüber hinaus werden zwei Informationsposter zu den ORIGIN Phase 3 und ORIGIN Extend Studien am 25. Oktober von Dr. Richard Lafayette vorgestellt.
Vera wird auch einen persönlichen und virtuellen R&D Tag in New York am 2. Oktober 2024 ausrichten, bei dem Experten wie Dr. Jonathan Barratt, Dr. Richard Lafayette und Dr. Brad Rovin über die erweiterten R&D Aktivitäten von Vera zu Atacicept diskutieren werden.
- Long-term results from ORIGIN Phase 2b trial of atacicept for IgAN to be presented at ASN Kidney Week 2024
- Two informational posters on ORIGIN Phase 3 and ORIGIN Extend trials accepted for presentation
- Upcoming R&D Day to discuss expanded atacicept R&D activities
- None.
- Two informational posters for ORIGIN Phase 3 and ORIGIN Extend trials of atacicept in IgAN accepted for presentation at Kidney Week;
- In-person and virtual R&D Day to discuss expanded atacicept R&D activities scheduled to take place in New York on October 2;
BRISBANE, Calif., Oct. 02, 2024 (GLOBE NEWSWIRE) -- Vera Therapeutics, Inc. (Nasdaq: VERA), a late clinical-stage biotechnology company focused on developing and commercializing transformative treatments for patients with serious immunological diseases, today announced that long-term results from the ORIGIN Phase 2b clinical trial of atacicept for the treatment of IgAN will be delivered in a late-breaking oral presentation, and two informational posters will describe the ORIGIN Phase 3 and ORIGIN Extend trials, at the American Society of Nephrology (ASN) Kidney Week 2024 in San Diego, California, from October 23 to 27.
ASN Kidney Week 2024 Presentation Details: | |
Title: | Long-term Results from the ORIGIN Phase 2b Study of Atacicept for the Treatment of IgAN |
Presenting Author: | Jonathan Barratt, M.D., Ph.D., F.R.C.P., The Mayer Professor of Renal Medicine, University of Leicester |
Abstract Number: | SA-OR102 |
Session: | Late-Breaking Science Orals - 2 |
Location: | Room 6C, Convention Center |
Date, Time: | Saturday, October 26, 2024, 5:20 PM – 5:30 PM PT |
Title: | ORIGIN 3: A Global Randomized, Controlled, Phase 3 Study of Atacicept in IgAN |
Presenting Author: | Richard Lafayette, M.D., F.A.C.P., Professor of Medicine, Nephrology and Director of the Stanford Glomerular Disease Center at Stanford University Medical Center |
Poster Number: | INFO09-FR |
Location: | Exhibit Hall, Convention Center |
Date, Time: | Friday, October 25, 10:00 AM – 12:00 PM PT |
Title: | ORIGIN Extend: A Long-Term Extension Study of Atacicept in IgAN |
Presenting Author: | Richard Lafayette, M.D., F.A.C.P., Professor of Medicine, Nephrology and Director of the Stanford Glomerular Disease Center at Stanford University Medical Center |
Poster Number: | INFO10-FR |
Location: | Exhibit Hall, Convention Center |
Date, Time: | Friday, October 25, 10:00 AM – 12:00 PM PT |
Upcoming R&D Day in New York
As previously announced, Vera will host an in-person and virtual R&D Day in New York, NY at 8:00 AM ET on Wednesday, October 2, 2024. The event will feature Jonathan Barratt, MD, PhD, FRCP (University of Leicester), Richard Lafayette, MD, FACP (Stanford University Medical Center), and Brad Rovin, MD (Ohio State University Wexner Medical Center), who will join the company’s management team to discuss Vera’s expanded atacicept R&D activities. A live question and answer session will follow the formal presentation. To register, click here.
About Vera
Vera Therapeutics is a late clinical-stage biotechnology company focused on developing treatments for serious immunological diseases. Vera’s mission is to advance treatments that target the source of immunological diseases in order to change the standard of care for patients. Vera’s lead product candidate is atacicept, a fusion protein self-administered as a subcutaneous injection once weekly that blocks both B-cell Activating Factor (BAFF) and A PRoliferation-Inducing Ligand (APRIL), which stimulate B cells and plasma cells to produce autoantibodies contributing to certain autoimmune diseases, including IgAN, also known as Berger’s disease, and lupus nephritis. In addition, Vera is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove medically useful. Vera is also developing MAU868, a monoclonal antibody designed to neutralize infection with BK virus (BKV), a polyomavirus that can have devastating consequences in certain settings such as kidney transplant. Vera retains all global developmental and commercial rights to atacicept and MAU868. For more information, please visit www.veratx.com.
About Atacicept
Atacicept is an investigational recombinant fusion protein that contains the soluble transmembrane activator and calcium-modulating cyclophilin ligand interactor (TACI) receptor that binds to the cytokines B-cell activating factor (BAFF) and A PRoliferation-Inducing Ligand (APRIL). These cytokines are members of the tumor necrosis factor family that promote B-cell survival and autoantibody production associated with certain autoimmune diseases, including IgAN and lupus nephritis.
The Phase 2b ORIGIN clinical trial of atacicept in IgAN met its primary and key secondary endpoints, with statistically significant and clinically meaningful proteinuria reductions and stabilization of eGFR versus placebo through 36 weeks. The safety profile during the randomized period was comparable between atacicept and placebo. Through 72 weeks, atacicept demonstrated further reductions in Gd-IgA1, hematuria, and proteinuria, as well as stabilization of eGFR reflecting a profile consistent with that of the general population without IgAN.
Atacicept has received FDA Breakthrough Therapy Designation for the treatment of IgAN, which reflects the FDA’s determination that, based on an assessment of data from the Phase 2b ORIGIN clinical trial, atacicept may demonstrate substantial improvement on a clinically significant endpoint over available therapies for patients with IgAN. Vera believes atacicept is positioned for best-in-class potential, targeting B cells and plasma cells to reduce autoantibodies and having been administered to more than 1,500 patients in clinical studies across different indications.
Forward-looking Statements
Statements contained in this press release regarding matters, events or results that may occur in the future are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, Vera’s anticipated presentations of clinical trial data, and Vera’s product candidates, strategy, and regulatory matters. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as “delivered,” “expanded,” “scheduled,” “substantial,” and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Vera’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks related to the regulatory approval process, results of earlier clinical trials may not be obtained in later clinical trials, preliminary results may not be predictive of topline results, risks and uncertainties associated with Vera’s business in general, the impact of macroeconomic and geopolitical events, and the other risks described in Vera’s filings with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management’s assumptions and estimates as of such date. Vera undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.
For more information, please contact:
Investor Contact:
Joyce Allaire
LifeSci Advisors
212-915-2569
jallaire@lifesciadvisors.com
Media Contact:
Madelin Hawtin
LifeSci Communications
MHawtin@lifescicomms.com
FAQ
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