Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
H101 + camrelizumab is a combination therapy consisting of an oncolytic adenovirus (H101) and a humanized monoclonal antibody targeting programmed cell death protein 1 (PD-1), known as camrelizumab. H101 is an E1B55KD-deleted recombinant human type 5 adenovirus that selectively replicates in and lyses tumor cells, also modulating the tumor microenvironment by downregulating CD47 expression to promote macrophage-mediated phagocytosis of cancer cells and increasing cytokine production (TNF, IL-12, IFN-γ). Camrelizumab blocks PD-1 on T lymphocytes, B cells, and NK cells to prevent its interaction with PD-L1/PD-L2 ligands expressed by tumor or antigen-presenting cells. This blockade restores immune function through activation of cytotoxic T lymphocytes against tumors. The combination has demonstrated synergistic anti-tumor effects in preclinical models by enhancing both innate and adaptive anti-tumor immunity[2][5][6]. It is being investigated primarily for solid tumors including glioblastoma and bladder cancer.
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 H101 + camrelizumab.