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Jasper Therapeutics Announces Briquilimab Presentations at the European Academy of Allergy and Clinical Immunology (EAACI) Annual Congress

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Jasper Therapeutics (NASDAQ: JSPR) announced the acceptance of four abstracts for presentation at the EAACI Congress 2025 in Glasgow, focusing on their novel antibody therapy briquilimab. The presentations will showcase initial clinical data from the SPOTLIGHT Phase 1b/2a study testing briquilimab in cold urticaria and symptomatic dermographism patients. The abstracts cover various aspects including results from the SPOTLIGHT study, protection against allergen-induced dermatitis in mice, disease control in chronic spontaneous urticaria patients, and effects on COPD-like features in asthma models. The presentations will take place on June 14-15, 2025, featuring both oral and poster sessions.
Jasper Therapeutics (NASDAQ: JSPR) ha annunciato l'accettazione di quattro abstract per la presentazione al Congresso EAACI 2025 a Glasgow, focalizzati sulla loro nuova terapia con anticorpi briquilimab. Le presentazioni mostreranno i primi dati clinici dello studio SPOTLIGHT di fase 1b/2a, che testa briquilimab in pazienti con orticaria da freddo e dermografismo sintomatico. Gli abstract trattano vari aspetti, tra cui i risultati dello studio SPOTLIGHT, la protezione contro la dermatite indotta da allergeni nei topi, il controllo della malattia in pazienti con orticaria spontanea cronica e gli effetti sulle caratteristiche simili alla BPCO in modelli di asma. Le presentazioni si terranno dal 14 al 15 giugno 2025, con sessioni orali e poster.
Jasper Therapeutics (NASDAQ: JSPR) anunció la aceptación de cuatro resúmenes para presentación en el Congreso EAACI 2025 en Glasgow, centrados en su novedosa terapia con anticuerpos briquilimab. Las presentaciones mostrarán datos clínicos iniciales del estudio SPOTLIGHT de fase 1b/2a que prueba briquilimab en pacientes con urticaria por frío y dermografismo sintomático. Los resúmenes cubren varios aspectos, incluyendo resultados del estudio SPOTLIGHT, protección contra dermatitis inducida por alérgenos en ratones, control de la enfermedad en pacientes con urticaria espontánea crónica y efectos en características similares a EPOC en modelos de asma. Las presentaciones tendrán lugar del 14 al 15 de junio de 2025, con sesiones orales y de póster.
Jasper Therapeutics (NASDAQ: JSPR)는 2025년 글래스고에서 열리는 EAACI 학회에서 자사의 새로운 항체 치료제 브리퀼리맙(briquilimab)에 관한 4개의 초록이 채택되었음을 발표했습니다. 발표에서는 찬 우드리카리아 및 증상성 피부문신 환자를 대상으로 한 SPOTLIGHT 1b/2a상 초기 임상 데이터가 소개됩니다. 초록들은 SPOTLIGHT 연구 결과, 쥐에서 알레르기 유발 피부염 보호 효과, 만성 자발성 두드러기 환자의 질병 조절, 천식 모델에서 COPD 유사 특징에 미치는 영향 등 다양한 주제를 다룹니다. 발표는 2025년 6월 14일부터 15일까지 구두 및 포스터 세션으로 진행됩니다.
Jasper Therapeutics (NASDAQ : JSPR) a annoncé l'acceptation de quatre résumés pour présentation au Congrès EAACI 2025 à Glasgow, portant sur leur nouvelle thérapie par anticorps briquilimab. Les présentations mettront en avant les premières données cliniques de l'étude SPOTLIGHT de phase 1b/2a testant briquilimab chez des patients atteints d'urticaire au froid et de dermographisme symptomatique. Les résumés couvrent divers aspects, notamment les résultats de l'étude SPOTLIGHT, la protection contre la dermatite allergique induite chez la souris, le contrôle de la maladie chez les patients atteints d'urticaire spontanée chronique, ainsi que les effets sur les caractéristiques similaires à la BPCO dans des modèles d'asthme. Les présentations auront lieu les 14 et 15 juin 2025, avec des sessions orales et des posters.
Jasper Therapeutics (NASDAQ: JSPR) gab die Annahme von vier Abstracts für die Präsentation auf dem EAACI Kongress 2025 in Glasgow bekannt, die sich auf ihre neuartige Antikörpertherapie Briquilimab konzentrieren. Die Präsentationen zeigen erste klinische Daten aus der SPOTLIGHT Phase 1b/2a Studie, in der Briquilimab bei Patienten mit Kälteurtikaria und symptomatischem Dermatographismus getestet wird. Die Abstracts behandeln verschiedene Aspekte, darunter Ergebnisse der SPOTLIGHT-Studie, Schutz vor allergeninduzierter Dermatitis bei Mäusen, Krankheitskontrolle bei Patienten mit chronischer spontaner Urtikaria und Auswirkungen auf COPD-ähnliche Merkmale in Asthma-Modellen. Die Präsentationen finden vom 14. bis 15. Juni 2025 in Form von Vorträgen und Poster-Sessions statt.
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Insights

Jasper to present promising briquilimab data for multiple mast cell diseases at EAACI, potentially expanding its market opportunities.

Jasper Therapeutics' upcoming presentations at the EAACI Congress highlight significant clinical progress for briquilimab, their novel anti-c-Kit antibody therapy. The most notable presentation will feature initial clinical data from the 180mg cohort in their SPOTLIGHT Phase 1b/2a study for inducible urticarias (CIndU) - specifically cold urticaria and symptomatic dermographism - that haven't responded to standard antihistamine treatment.

The company will also present updated results from their Phase 1b/2a study in chronic spontaneous urticaria (CSU), which reportedly demonstrates "rapid, clinically meaningful disease-control" - language that suggests positive efficacy signals. The preclinical presentations on briquilimab's effects in dermatitis and asthma/COPD models indicate Jasper is exploring broader applications beyond urticaria.

This multi-indication approach is strategically sound as mast cell dysregulation underlies numerous allergic and inflammatory conditions. By targeting c-Kit (CD117), a receptor crucial for mast cell development and function, briquilimab represents a potential platform therapy that could address several diseases with significant unmet needs. The presentation of clinical data at a prestigious allergology conference provides important visibility among key opinion leaders who influence treatment guidelines and prescription patterns.

REDWOOD CITY, Calif., June 03, 2025 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (Nasdaq: JSPR) (Jasper), a clinical stage biotechnology company focused on development of briquilimab, a novel antibody therapy targeting c-Kit (CD117) to address mast cell driven diseases such as chronic spontaneous urticaria (CSU), chronic inducible urticaria (CIndU) and asthma, today announced that four abstracts have been accepted for presentation at the EAACI Congress 2025, to be held June 13-16, 2025 in Glasgow, United Kingdom. Jasper will present initial clinical data from patients enrolled in the 180mg cohort of the SPOTLIGHT Phase 1b/2a study evaluating briquilimab in subcutaneous briquilimab in cold urticaria (ColdU) or symptomatic dermographism (SD) during an oral session on Saturday, June 14.

Details of the presentations are as follows:

Abstract Title: Initial Results from SPOTLIGHT, a Phase 1b/2a Dose Escalation Study of the anti-c-Kit Briquilimab Antibody in Adults with Inducible Urticaria (CIndU) Who Remain Symptomatic Despite H-1 Antihistamine Treatment
Abstract Number: 269
Session Type/Title: Oral Abstract Session on Clinical Trials (OAS-CT2, Clinical Trials on Dermatology)
Presentation Date/Time: June 14, 3:00-4:30pm

Abstract Title: A Single Dose of Briquilimab, an Anti-Human c-Kit (CD117)-Antibody, Protects Against Relapse of Epicutaneous Allergen-Induced Dermatitis in Mice Expressing Chimeric Human/Mouse CD117
Abstract Number: 523
Session Type/Title: Thematic Poster Session (Biologicals 02)
Presentation Date/Time: June 14, 12:00-1:00pm

Abstract Title: Briquilimab Demonstrates Rapid, Clinically Meaningful Disease-Control in Adults with Chronic Spontaneous Urticaria (CSU): Updated Results from Phase 1b/2a Study
Abstract Number: 100281
Session Type/Title: Flash Talk (L-FT08 Dermatology)
Presentation Date/Time: June 15, 12:45-1:45pm

Abstract Title: Targeting Mast Cells with Briquilimab, an Anti-Human c-Kit (CD117)-Antibody, Mitigates COPD-Like Features in an Allergen and Cigarette Smoke-Exacerbated Asthma Model Using Humanized h/mCD117 Mice
Abstract Number: 537
Session Type/Title: Thematic Poster Session (Asthma 07),
Presentation Date/Time: June 15, 12:45-1:45pm

About Jasper

Jasper is a clinical-stage biotechnology company focused on developing briquilimab as a therapeutic for chronic mast cell diseases. Briquilimab is a targeted aglycosylated monoclonal antibody that blocks stem cell factor from binding to the cell-surface receptor KIT, thereby inhibiting signaling through the receptor. This inhibition disrupts the critical survival signal, leading to the depletion of the mast cells via apoptosis which removes the underlying source of the inflammatory response in mast cell driven diseases such as chronic urticaria and asthma. Jasper is currently conducting clinical studies of briquilimab as a treatment in patients with CSU, CIndU or asthma. Briquilimab has a demonstrated efficacy and safety profile in patients and healthy volunteers, with positive clinical outcomes in CSU and CIndU. For more information, please visit us at www.jaspertx.com.

Forward-Looking Statements

Certain statements included in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are sometimes accompanied by words such as “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “should,” “would,” “plan,” “predict,” “potential,” “seem,” “seek,” “future,” “outlook” and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding briquilimab’s potential, including with respect to its potential in mast cell driven diseases such as CSU, CIndU, and asthma; and Jasper’s presentations at the EAACI Annual Congress. These statements are based on various assumptions, whether or not identified in this press release, and on the current expectations of Jasper and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as, and must not be relied on by an investor as, a guarantee, an assurance, a prediction or a definitive statement of fact or probability. Many actual events and circumstances are beyond the control of Jasper. These forward-looking statements are subject to a number of risks and uncertainties, including general economic, political and business conditions; the risk that the potential product candidates that Jasper develops may not progress through clinical development or receive required regulatory approvals within expected timelines or at all; the risk that clinical trials may not confirm any safety, potency or other product characteristics described or assumed in this press release; the risk that prior test, study and trial results may not be replicated in continuing or future studies and trials; the risk that Jasper will be unable to successfully market or gain market acceptance of its product candidates; the risk that prior study results may not be replicated; the risk that Jasper’s product candidates may not be beneficial to patients or successfully commercialized; patients’ willingness to try new therapies and the willingness of physicians to prescribe these therapies; the effects of competition on Jasper’s business; the risk that third parties on which Jasper depends for laboratory, clinical development, manufacturing and other critical services will fail to perform satisfactorily; the risk that Jasper’s business, operations, clinical development plans and timelines, and supply chain could be adversely affected by the effects of health epidemics; the risk that Jasper will be unable to obtain and maintain sufficient intellectual property protection for its investigational products or will infringe the intellectual property protection of others; and other risks and uncertainties indicated from time to time in Jasper’s filings with the SEC, including its Annual Report on Form 10-K for the year ended December 31, 2024 and subsequent Quarterly Reports on Form 10-Q. If any of these risks materialize or Jasper’s assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. While Jasper may elect to update these forward-looking statements at some point in the future, Jasper specifically disclaims any obligation to do so. These forward-looking statements should not be relied upon as representing Jasper’s assessments of any date subsequent to the date of this press release. Accordingly, undue reliance should not be placed upon the forward-looking statements.

Contacts:

Alex Gray (investors)
Jasper Therapeutics
650-549-1454 
agray@jaspertherapeutics.com

Joyce Allaire (investors)
LifeSci Advisors
617-435-6602
jallaire@lifesciadvisors.com

Lauren Walker (media)
Real Chemistry
646-564-2156
lbarbiero@realchemistry.com


FAQ

What will Jasper Therapeutics (JSPR) present at EAACI Congress 2025?

Jasper Therapeutics will present four abstracts about briquilimab, including initial clinical data from the SPOTLIGHT Phase 1b/2a study and results from various preclinical and clinical studies in urticaria and asthma models.

When and where will JSPR present their briquilimab data?

The presentations will take place on June 14-15, 2025, at the EAACI Congress in Glasgow, United Kingdom.

What conditions is Jasper Therapeutics' briquilimab being developed to treat?

Briquilimab is being developed to treat mast cell driven diseases including chronic spontaneous urticaria (CSU), chronic inducible urticaria (CIndU), and asthma.

What is the mechanism of action of JSPR's briquilimab?

Briquilimab is a novel antibody therapy targeting c-Kit (CD117) to address mast cell driven diseases.

What is the current development stage of Jasper Therapeutics' briquilimab?

Briquilimab is currently in Phase 1b/2a clinical trials, as demonstrated by the SPOTLIGHT study in cold urticaria and symptomatic dermographism patients.
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