Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PRaG 3.0 is an investigational combination immunotherapy regimen being evaluated for the treatment of HER2-positive advanced refractory solid tumors. Developed as an investigator-initiated trial by the Second Affiliated Hospital of Soochow University, the regimen integrates disitamab vedotin (RC48-ADC)—a humanized anti-HER2 antibody conjugated to the cytotoxic payload monomethyl auristatin E (MMAE)—with hypofractionated radiotherapy, a PD-1/PD-L1 inhibitor, and the sequential administration of the cytokines GM-CSF and IL-2. The mechanism of action involves direct HER2-targeted cell killing and payload-mediated microtubule inhibition, complemented by radiotherapy-induced immunogenic cell death and immune checkpoint blockade. The sequential addition of GM-CSF and IL-2 is intended to further stimulate dendritic cell maturation and T-cell proliferation, creating a robust anti-tumor immune response in patients who have failed standard therapies.
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 disitamab vedotin + radiotherapy + PD-1 inhibitor + GM-CSF + IL-2.