Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Evorpacept is a recombinant fusion protein and immunotherapy agent designed to block the CD47–SIRPα pathway, which is a key immune checkpoint exploited by cancer cells to evade phagocytosis. By binding with high affinity to CD47 on tumor cells, evorpacept prevents its interaction with SIRPα on phagocytic cells (such as macrophages and dendritic cells), thereby abrogating the "don't eat me" signal that inhibits immune-mediated clearance of cancer cells[1][2][3]. This blockade enhances macrophage-mediated phagocytosis, stimulates dendritic cell activity, promotes T-cell activation through cross-priming, and can improve the efficacy of other anti-cancer therapies including monoclonal antibodies, antibody-drug conjugates (ADCs), and checkpoint inhibitors[2][5][6]. Evorpacept has demonstrated a favorable safety profile in clinical trials compared to earlier anti-CD47 agents due to its engineered inactive Fc domain[6]. It is being developed primarily for various solid tumors and hematologic malignancies by ALX Oncology in collaboration with several partners.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on evorpacept.