Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
DSPE-DOTA-Gd is a gadolinium-based contrast agent designed for use in magnetic resonance imaging (MRI). It consists of a lipid derivative (1,2-distearoyl-sn-glycero-3-phosphoethanolamine or DSPE) conjugated to DOTA (1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic acid), which acts as a chelator for gadolinium ions (Gd3+). The resulting compound can be incorporated into liposomes or lipid nanoparticles to create MRI-detectable formulations with high relaxivity and stability. This design allows for enhanced imaging contrast and site-targeted delivery in molecular imaging studies. The agent has been shown to have high longitudinal relaxivity and low risk of transmetallation with other metal ions such as zinc, contributing to its biocompatibility. It is being investigated primarily as an MRI enhancer for applications including molecular imaging and targeted drug delivery[1][2][4][7].
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 DSPE-DOTA-Gd.