Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This investigational cell-based therapy consists of autologous umbilical cord blood-derived mononuclear cells (UCB-MNCs) developed by Dr. Timothy J. Nelson and the Todd and Karen Wanek Family Program for Hypoplastic Left Heart Syndrome at Mayo Clinic. The therapy involves collecting umbilical cord blood from infants diagnosed with hypoplastic left heart syndrome (HLHS) at birth, processing it to isolate mononuclear stem cells, and delivering them via intramyocardial injection into the right ventricular myocardium during Stage II palliation surgery (Glenn procedure), typically performed at 3-13 months of age. The goal is to strengthen the underdeveloped right ventricle through regenerative medicine. However, a Phase IIb multicenter trial (AutoCell-S2) involving 95 children found that the treatment failed to enhance cardiac function and was associated with unfavorable changes in longitudinal cardiac strain and higher rates of serious adverse events compared to controls.
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 autologous umbilical cord blood-derived mononuclear cells.