Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GCAN-101 is an experimental, plasma-derived intravenous immunoglobulin (IVIG) formulation developed as an immunostimulant for the treatment of various cancers, most notably metastatic melanoma. Developed by Gammacan International, the drug consists of purified polyclonal antibodies harvested from healthy donors. The therapeutic rationale was based on the observation that certain naturally occurring antibodies in the human immune repertoire can recognize and neutralize tumor-promoting factors or directly stimulate an anti-tumor immune response. Clinical development reached Phase 2 trials for melanoma, but the program was discontinued in the late 2000s following financial difficulties and restructuring at Gammacan International.
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 GCAN-101.