Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PKHB1 is a synthetic peptide that mimics the C-terminal binding domain of thrombospondin-1 (TSP-1) and functions as a CD47 agonist. It induces immunogenic cell death (ICD) in various cancer cells, including hematological malignancies such as acute lymphoblastic leukemia (ALL), chronic lymphocytic leukemia (CLL), and solid tumors like breast cancer, particularly triple-negative subtypes[2][5][6]. The mechanism of action involves caspase-independent, calcium-dependent cell death associated with mitochondrial alterations, reactive oxygen species production, intracellular Ca2+ accumulation, and exposure/release of damage-associated molecular patterns (DAMPs) such as calreticulin, HSP70/90, ATP, and HMGB1[2][4][5]. This leads to dendritic cell maturation and activation of antitumor T-cell responses. In vivo studies show that PKHB1 reduces tumor volume/weight and promotes intratumoral CD8+ T-cell infiltration in breast cancer models[2]. Additionally, it has demonstrated antiviral effects by inhibiting herpes simplex virus type 1 replication in preclinical models[4]. PKHB1 is currently under preclinical investigation for oncology indications.
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 PKHB1.