Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Liafensine is a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI), also known as a triple monoamine reuptake inhibitor. It was originally developed by Bristol Myers Squibb for the treatment of major depressive disorder and later investigated for treatment-resistant depression. Liafensine acts by inhibiting the reuptake of serotonin, norepinephrine, and dopamine in the brain, thereby increasing their extracellular concentrations. Recent development has been led by Denovo Biopharma using a biomarker-guided approach to identify patients most likely to respond to therapy[1][6][8]. In clinical trials, liafensine demonstrated efficacy comparable to established antidepressants but did not show superiority over them in earlier studies; however, recent biomarker-guided trials have shown significant improvement in depressive symptoms among DGM4-positive patients with treatment-resistant depression[7][10].
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 liafensine.