Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This agent is a combination of **ruxoprubart** (formerly NM8074) and **eculizumab**. Ruxoprubart is a humanized monoclonal antibody targeting the Bb domain of complement factor B, thus blocking the alternative pathway of complement activation while sparing the classical pathway. Eculizumab is a monoclonal antibody that inhibits terminal complement protein C5, preventing the formation of the membrane attack complex. The combination is being investigated for **paroxysmal nocturnal hemoglobinuria (PNH)**, particularly in patients with inadequate response to eculizumab monotherapy. The rationale is that blocking both factor B (upstream in the alternative pathway) and C5 (terminal pathway) may provide greater control of complement-mediated hemolysis and associated symptoms[1][2][5].
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 ruxoprubart + eculizumab.