STOCK TITAN

Upstream Bio to Present Mechanistic Insights into Verekitug’s Enhanced Potency via TSLP Receptor Targeting at European Academy of Allergy and Clinical Immunology (EAACI) Congress 2025

Rhea-AI Impact
(Low)
Rhea-AI Sentiment
(Neutral)
Tags
conferences
Upstream Bio (Nasdaq: UPB) announced an upcoming presentation at the European Academy of Allergy and Clinical Immunology (EAACI) Congress 2025 in Glasgow, UK. The presentation will showcase translational pharmacology modeling data for their drug verekitug, which targets the TSLP receptor for inflammatory diseases, particularly severe respiratory disorders. The data demonstrates verekitug's enhanced potency compared to treatments targeting the TSLP ligand, such as tezepelumab. Dr. Ashish Kalra, VP of Translational Research, will present these findings on June 15, 2025, focusing on the in silico system pharmacology modeling insights that explain the drug's superior potency mechanism.
Upstream Bio (Nasdaq: UPB) ha annunciato una presentazione imminente al Congresso 2025 della European Academy of Allergy and Clinical Immunology (EAACI) che si terrà a Glasgow, Regno Unito. La presentazione mostrerà i dati di modellazione farmacologica traslazionale per il loro farmaco verekitug, che agisce sul recettore TSLP per le malattie infiammatorie, in particolare i disturbi respiratori gravi. I dati evidenziano la maggiore potenza di verekitug rispetto ai trattamenti che mirano al ligando TSLP, come tezepelumab. Il dott. Ashish Kalra, vicepresidente della Ricerca Traslazionale, presenterà questi risultati il 15 giugno 2025, concentrandosi sulle intuizioni della modellazione farmacologica di sistema in silico che spiegano il meccanismo di potenza superiore del farmaco.
Upstream Bio (Nasdaq: UPB) anunció una próxima presentación en el Congreso 2025 de la European Academy of Allergy and Clinical Immunology (EAACI) que se celebrará en Glasgow, Reino Unido. La presentación mostrará datos de modelado farmacológico traslacional para su medicamento verekitug, que se dirige al receptor TSLP para enfermedades inflamatorias, especialmente trastornos respiratorios graves. Los datos demuestran la mayor potencia de verekitug en comparación con tratamientos que apuntan al ligando TSLP, como tezepelumab. El Dr. Ashish Kalra, vicepresidente de Investigación Traslacional, presentará estos hallazgos el 15 de junio de 2025, enfocándose en los conocimientos del modelado farmacológico sistémico in silico que explican el mecanismo de potencia superior del medicamento.
업스트림 바이오(Nasdaq: UPB)는 영국 글래스고에서 열리는 2025년 유럽 알레르기 및 임상면역학 학회(EAACI) 총회에서 곧 발표를 할 예정이라고 발표했습니다. 이번 발표에서는 염증성 질환, 특히 중증 호흡기 질환을 대상으로 하는 TSLP 수용체를 표적으로 하는 약물 베레키투그(vereKitug)의 전이 약리학 모델링 데이터를 선보일 예정입니다. 데이터는 테제펠루맙(tezepelumab)과 같은 TSLP 리간드를 표적으로 하는 치료제에 비해 베레키투그의 향상된 효능을 보여줍니다. 전이 연구 부사장인 아시시 칼라 박사는 2025년 6월 15일 이 약물의 우수한 효능 메커니즘을 설명하는 인 실리코 시스템 약리학 모델링 통찰을 중심으로 이 결과를 발표할 예정입니다.
Upstream Bio (Nasdaq : UPB) a annoncé une présentation prochaine lors du Congrès 2025 de l'European Academy of Allergy and Clinical Immunology (EAACI) à Glasgow, Royaume-Uni. Cette présentation mettra en avant des données de modélisation pharmacologique translationnelle pour leur médicament verekitug, ciblant le récepteur TSLP pour les maladies inflammatoires, notamment les troubles respiratoires sévères. Les données démontrent la puissance accrue de verekitug par rapport aux traitements ciblant le ligand TSLP, comme le tezépélumab. Le Dr Ashish Kalra, vice-président de la recherche translationnelle, présentera ces résultats le 15 juin 2025, en se concentrant sur les insights issus de la modélisation pharmacologique systémique in silico qui expliquent le mécanisme de puissance supérieure du médicament.
Upstream Bio (Nasdaq: UPB) kündigte eine bevorstehende Präsentation auf dem Kongress der European Academy of Allergy and Clinical Immunology (EAACI) 2025 in Glasgow, Großbritannien, an. Die Präsentation wird translational-pharmakologische Modellierungsdaten für ihr Medikament Verekitug vorstellen, das den TSLP-Rezeptor bei entzündlichen Erkrankungen, insbesondere schweren Atemwegserkrankungen, adressiert. Die Daten zeigen die erhöhte Wirksamkeit von Verekitug im Vergleich zu Behandlungen, die den TSLP-Liganden, wie Tezepelumab, anvisieren. Dr. Ashish Kalra, Vizepräsident der Translationalen Forschung, wird diese Ergebnisse am 15. Juni 2025 präsentieren und dabei Einblicke in die in silico Systempharmakologie-Modellierung geben, die den überlegenen Wirkmechanismus des Medikaments erklären.
Positive
  • None.
Negative
  • None.

WALTHAM, Mass., June 05, 2025 (GLOBE NEWSWIRE) -- Upstream Bio, Inc. (Nasdaq: UPB), a clinical-stage company developing treatments for inflammatory diseases, with an initial focus on severe respiratory disorders, today announced an upcoming presentation at the European Academy of Allergy and Clinical Immunology (EAACI) Congress 2025 in Glasgow, UK, on Sunday, June 15, 2025. The presentation features translational pharmacology modeling data that supports Thymic Stromal Lymphopoietin (TSLP) receptor targeting with verekitug as a mechanism for greater potency when compared to treatment approaches that target the TSLP ligand.

Presentation details:

Presentation Title: In silico system pharmacology modeling provides insights into a mechanism for greater potency of TSLP/TSLPR pathway inhibition with verekitug, a novel antibody antagonist of the TSLP receptor, as compared with tezepelumab

Presenting Author: Ashish Kalra, PhD, Vice President, Translational Research, Upstream Bio

Poster Number: D3.113

Session: TPS55 – Asthma 06

Presentation Date and Time: Sunday, June 15, 2025 – 12:45 - 13:45 BST

About TSLP and TSLPR Blockade
Thymic Stromal Lymphopoietin (TSLP) is a cytokine that is a key driver of the inflammatory response in major allergic and inflammatory diseases, such as asthma, where disruption of TSLP signaling has been clinically validated as an effective therapeutic strategy.

TSLP activation is one of the first events in the inflammatory cascade stimulated by allergens, viruses and other triggers, initiating the activation of downstream targets such as IL-4, IL-5, IL-13, IL-17 and IgE. Because TSLP is a target upstream in the inflammatory cascade, blocking the TSLP receptor (TSLPR) presents an opportunity for a single treatment to impact the drivers of multiple pathological inflammatory processes across a broad set of diseases.

About Verekitug
Verekitug is a novel recombinant fully human immunoglobulin G1 (IgG1) monoclonal antibody (mAb) that binds to the TSLP receptor and inhibits proinflammatory signaling initiated by TSLP. It is the only monoclonal antibody currently in clinical development that targets and inhibits the TSLP receptor. Verekitug is currently being evaluated in two separate multi-national, placebo-controlled, randomized Phase 2 clinical trials, the VALIANT trial in patients with severe asthma (NCT06196879) and the VIBRANT trial in patients with chronic rhinosinusitis with nasal polyps (CRSwNP) (NCT06164704). Upstream Bio is also initiating a Phase 2 clinical trial (NCT06981078) of verekitug in patients with moderate-to-severe chronic obstructive pulmonary disease (COPD).

In preclinical studies, verekitug demonstrated high occupancy of the TSLP receptor and potent inhibition of TSLP signaling. Additionally, verekitug inhibited cytokine production from both CD4+ T cells and ILC2 cells and completely suppressed skin allergic reactions in a non-human primate model, suggesting that it may be effective against multiple types of inflammation.

Three clinical trials have been completed for verekitug, including a Phase 1 single-ascending dose (SAD) clinical trial and a Phase 1b multiple-ascending dose (MAD) clinical trial. In these trials, verekitug was well tolerated, had no clinically meaningful immunogenicity, and showed a predictable and consistent pharmacokinetic profile and high subcutaneous bioavailability.

About Upstream Bio
Upstream Bio is a clinical-stage biotechnology company developing treatments for inflammatory diseases, with an initial focus on severe respiratory disorders. The Company is developing verekitug, the only known antagonist currently in clinical development that targets the receptor for thymic stromal lymphopoietin (TSLP), a cytokine which is a clinically validated driver of inflammatory response positioned upstream of multiple signaling cascades that affect a variety of immune mediated diseases. The Company has advanced this highly potent monoclonal antibody into separate Phase 2 trials for the treatment of severe asthma and chronic rhinosinusitis with nasal polyps and is initiating development in chronic obstructive pulmonary disease. Upstream Bio’s team is committed to maximizing verekitug’s unique attributes to address the substantial unmet needs for patients underserved by today’s standard of care. To learn more, please visit www.upstreambio.com.

Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, each as amended. These statements may be identified by words such as “aims,” “anticipates,” “believes,” “continue,” “could,” “estimates,” “expects,” “forecasts,” “goal,” “intends,” “may,” “plans,” “possible,” “potential,” “predict,” “project,” “seeks,” “should,” “target,” “will” and variations of these words or similar expressions. Any statements in this press release that are not statements of historical fact may be deemed to be forward-looking statements. These forward-looking statements include, without limitation, express or implied statements regarding: the global development of verekitug for the treatment of severe asthma, CRSwNP and COPD, including the initiation, timing, progress and results of ongoing and planned clinical trials; and expectations regarding the differentiation, safety, efficacy, tolerability, and/or extended dosing interval of verekitug. Any forward-looking statements in this press release are based on the Company’s current expectations, estimates and projections only as of the date of this release and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. Readers are cautioned that actual results, levels of activity, safety, efficacy, performance or events and circumstances could differ materially from those expressed or implied in the Company’s forward-looking statements due to a variety of risks and uncertainties, which include, without limitation, risks and uncertainties related to: Upstream Bio’s ability to advance verekitug through clinical development, and to obtain regulatory approval of and ultimately commercialize verekitug on the expected timeline, if at all; the initiation, timing, progress and results of clinical trials; Upstream Bio’s ability to fund its development activities and achieve development goals; Upstream Bio’s dependence on third parties to conduct clinical trials and manufacture verekitug, and commercialize verekitug, if approved; Upstream Bio’s ability to attract, hire and retain key personnel, and protect its intellectual property; Upstream Bio’s financial condition and need for substantial additional funds in order to complete development activities and commercialize verekitug, if approved; regulatory developments and approval processes of the U.S. Food and Drug Administration and comparable foreign regulatory authorities; Upstream Bio’s competitors and industry; and other risks and uncertainties described in greater detail under the caption “Risk Factors” in Upstream Bio’s most recent Annual Report on Form 10-K and Quarterly Report on Form 10-Q, as well as any subsequent filings with the SEC. Any forward-looking statements represent Upstream Bio’s views only as of today and should not be relied upon as representing its views as of any subsequent date. Upstream Bio explicitly disclaims any obligation or undertaking to update any forward-looking statements contained herein to reflect any change in its expectations or any changes in events, conditions or circumstances on which any such statement is based except to the extent required by law, and claims the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995.



Investor and Media Contact:
Meggan Buckwell
Director, Corporate Communications and Investor Relations
ir@upstreambio.com

FAQ

What will Upstream Bio (UPB) present at EAACI Congress 2025?

Upstream Bio will present translational pharmacology modeling data showing how verekitug's TSLP receptor targeting mechanism provides greater potency compared to TSLP ligand-targeting treatments.

When and where is Upstream Bio's (UPB) presentation at EAACI Congress 2025?

The presentation is scheduled for Sunday, June 15, 2025, from 12:45 - 13:45 BST in Glasgow, UK.

Who will present Upstream Bio's (UPB) research at EAACI Congress 2025?

Dr. Ashish Kalra, Vice President of Translational Research at Upstream Bio, will present the research.

What is verekitug and how does it differ from other treatments?

Verekitug is Upstream Bio's novel antibody antagonist that targets the TSLP receptor, showing greater potency compared to treatments like tezepelumab that target the TSLP ligand.
UpStream Bio Inc.

NASDAQ:UPB

UPB Rankings

UPB Latest News

UPB Stock Data

502.97M
40.12M
19.8%
87.82%
6.91%
Biotechnology
Pharmaceutical Preparations
Link
United States
WALTHAM