Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Turnobi is an intravenous formulation of L-citrulline, a non-essential amino acid that serves as a precursor in the nitric oxide (NO) synthesis pathway by being converted to L-arginine and subsequently to NO by nitric oxide synthase. By augmenting endogenous NO production, Turnobi is being developed to improve endothelial function, enhance vasodilation, and modulate microvascular blood flow, particularly in conditions characterized by vaso-occlusion and endothelial dysfunction such as sickle cell disease and acute lung injury. Clinical development has been led through academic–industry collaboration, notably Vanderbilt University and Asklepion Pharmaceuticals, with Phase 2–3 studies evaluating its ability to abort or lessen vaso-occlusive crises in pediatric and young adult patients with sickle cell disease and to prevent or treat acute lung injury in critical care settings.[1][5][7][11][13][17]
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 Turnobi.