Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
NX1907 is a preclinical-stage small molecule drug candidate being developed by NEXTGEN Bioscience for the treatment of idiopathic pulmonary fibrosis (IPF). It functions as a dual inhibitor of macrophage migration inhibitory factor (MIF) and D-dopachrome tautomerase (D-DT, also known as MIF-2). These two cytokines are structurally related and share the CD74 receptor, playing critical roles in promoting the inflammatory and fibrotic processes that characterize IPF. By simultaneously inhibiting both MIF and D-DT, NX1907 aims to provide superior anti-fibrotic activity compared to single-target inhibitors, potentially offering a new therapeutic approach to slow disease progression and improve lung function in patients with fibrotic lung diseases.
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 NX1907.