IPH5201, an Anti-CD39 mAb, as Monotherapy or in Combination with Durvalumab in Advanced Solid Tumors

The adenosine pathway is a source of emerging targets in cancer immunotherapy. IPH5201 is a mAb that targets the adenosine pathway by blocking human CD39 enzymatic activity. In this first-in-human, phase 1 study, IPH5201 as monotherapy or in combination with durvalumab was well tolerated with a manageable safety profile in patients with advanced solid tumors. Preliminary evidence for disease stabilization and reduction of tumoral CD39 enzymatic activity were observed.

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Publication Details

Journal
Cancer Research Communications
Published
2025-09-01
DOI
https://doi.org/10.1158/2767-9764.crc-25-0361
Citations
1
Primary Topic
Adenosine and Purinergic Signaling
Type
article
Field-Weighted Citation Impact
1.12

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article

IPH5201, an Anti-CD39 mAb, as Monotherapy or in Combination with Durvalumab in Advanced Solid Tumors

Meredith McKean, Vicky Barnhart, Eric Tu, Raymond Mager et al.
1 citations
Cancer Research Communications
Adenosine and Purinergic Signaling
1.12
article

IPH5201, an Anti-CD39 mAb, as Monotherapy or in Combination with Durvalumab in Advanced Solid Tumors

Meredith McKean, Vicky Barnhart, Eric Tu, Raymond Mager, Martina Imbimbo, Chunling Fan, Carine Paturel, Yun He, Steven Eck, Paula G. Fraenkel, Antoîne Italiano, Elina Murtomaki, Benedito A. Carneiro, Zachary A. Cooper, Patricia Martín-Romano, Teresa Macarulla, Antoine Hollebecque, John D. Powderly, Arsène‐Bienvenu Loembé, Eduardo Castañón Álvarez, Agnes Boyer Chamard
article en
1 citations

Abstract

The adenosine pathway is a source of emerging targets in cancer immunotherapy. IPH5201 is a mAb that targets the adenosine pathway by blocking human CD39 enzymatic activity. In this first-in-human, phase 1 study, IPH5201 as monotherapy or in combination with durvalumab was well tolerated with a manageable safety profile in patients with advanced solid tumors. Preliminary evidence for disease stabilization and reduction of tumoral CD39 enzymatic activity were observed.

Cancer Research CommunicationsVol. 5(9)
AstraZeneca (United Kingdom) (GB), Hebron University (PS), Université de Bordeaux (FR), Brown University (US), Institut Gustave Roussy (FR), Centre Hospitalier Universitaire Vaudois (CH), AstraZeneca (South Korea) (KR), Carolina BioOncology Institute (US), Massachusetts Medical Society (US), Sarah Cannon (US), AstraZeneca (Brazil) (BR), Gobierno de Navarra (ES), Vall d'Hebron Hospital Universitari (ES), Institut Bergonié (FR), Clinica Universidad de Navarra (ES), Tennessee Oncology (US), Innate Pharma (France) (FR), AstraZeneca (United States) (US), Lifespan (US), Vall d'Hebron Institute of Oncology (ES)
AstraZeneca
Openalex Percentile: Top 21%
Adenosine and Purinergic Signaling
1.12
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