Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a four-drug investigational combination comprising **nivolumab** (a monoclonal antibody PD-1 checkpoint inhibitor), **ipilimumab** (a monoclonal antibody CTLA-4 checkpoint inhibitor), **hydroxychloroquine** (a small molecule antimalarial and autophagy inhibitor), and **NG-350A** (a next-generation blood-stable adenoviral vector engineered to express a potent agonist anti-CD40 monoclonal antibody specifically within tumor tissue). The combination represents a multi-modal approach intended to enhance anti-tumor immune responses through checkpoint blockade, immune activation, and inhibition of autophagy, with the oncolytic viral vector (NG-350A) potentially augmenting T-cell priming within the tumor microenvironment. NG-350A is being developed by Akamis Bio. This combination is currently experimental, with components (nivolumab + ipilimumab) already approved in various cancers, but the quadruple regimen itself is in early-phase investigation, particularly in solid tumors, including advanced/metastatic epithelial tumors.
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 nivolumab + ipilimumab + hydroxychloroquine + NG-350A.