Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Cavit + ferric sulfate is a dental treatment combination being investigated by Virginia Commonwealth University for use in pulpotomy procedures in primary teeth. This approach utilizes a 15.5% ferric sulfate solution as a hemostatic agent to control pulpal bleeding from the pulp stumps, followed by the application of Cavit (a non-eugenol temporary restorative material manufactured by 3M) as a base material. Cavit is composed of zinc oxide, zinc sulfate, and calcium salts, and is known for its excellent sealing capability and induction of an alkaline pH that may promote hard tissue formation. The combination is designed to address the high rate of internal resorption and radiological failure associated with traditional eugenol-containing zinc oxide (ZOE) materials, such as IRM, when used in conjunction with ferric sulfate. By eliminating the release of free eugenol, the treatment aims to provide a more stable environment that avoids the inflammatory responses and failures typically seen in vital pulp therapy in children with pulpitis.
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 Cavit + ferric sulfate.