Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
E-602 + cemiplimab is an investigational combination therapy comprised of E-602, a first-in-class human sialidase enzyme therapeutic developed by Palleon Pharmaceuticals, and cemiplimab, an approved anti-PD-1 monoclonal antibody (marketed as Libtayo)[1][3][4][6]. E-602 is designed to enzymatically degrade immunosuppressive sialoglycans found on hypersialylated tumors and immune cells, effectively restoring antitumor immunity by reversing glyco-immune checkpoint–mediated suppression. Cemiplimab blocks PD-1, an immune checkpoint, to promote T-cell mediated immune response against cancer cells. The combination was evaluated in Phase 1/2 trials (GLIMMER-01) for patients with advanced, PD-(L)1-resistant solid tumors including melanoma, non-small cell lung cancer (NSCLC), and esophagogastric junction cancer. The combination achieved tumor desialylation, reduced pro-tumor macrophages (CD163+), increased cytokine levels, and showed early antitumor activity with no dose-limiting toxicities[1][2][4][6].
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 E-602 + cemiplimab.