Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy involves the use of Ganoderma lucidum spore powder as an adjuvant to standard chemotherapy (specifically gemcitabine or cisplatin) for the treatment of non-small cell lung carcinoma (NSCLC). Ganoderma lucidum, a medicinal mushroom also known as Reishi or Lingzhi, contains bioactive compounds such as polysaccharides and triterpenes that are thought to possess immunomodulatory, antioxidant, and antineoplastic properties. In this clinical context, the spores are administered orally to potentially enhance the therapeutic efficacy of chemotherapy while mitigating common toxicities, including bone marrow suppression and gastrointestinal mucosal damage. The intervention is currently being evaluated in a Phase 2 randomized, placebo-controlled trial led by Gao Yajie at The First Affiliated Hospital of Dalian Medical University to assess its impact on quality of life and various biochemical markers of oxidative stress and inflammation.
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 Ganoderma lucidum spore + chemotherapy.