Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Dextran sulfate low molecular weight (LMW-DS) is a sulfated polysaccharide derivative currently being investigated as a potential disease-modifying therapy for amyotrophic lateral sclerosis (ALS). Developed in part by researchers at Oslo University Hospital, LMW-DS is hypothesized to interfere with the pathological aggregation of TAR DNA-binding protein 43 (TDP-43), a hallmark proteinopathy found in the motor neurons of nearly all ALS patients. By binding to misfolded proteins, LMW-DS may prevent the formation of toxic aggregates and facilitate their clearance. Additionally, the drug is thought to modulate neuroinflammatory pathways and stabilize the blood-brain barrier, which are often compromised in neurodegenerative conditions. Clinical trials, such as the Phase 2 study conducted by Oslo University Hospital, evaluate the safety and efficacy of LMW-DS administered via intravenous infusion to slow the progression of motor neuron loss and functional decline in ALS patients.
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 dextran sulfate low molecular weight.