Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Laresse is a temporary dermal filler developed by FzioMed, a U.S.-based medical device company. It is composed of absorbable medical polymers, specifically carboxymethylcellulose (CMC) and polyethylene oxide (PEO). Classified as a medical device rather than a traditional pharmaceutical drug, Laresse is intended for the correction of facial soft tissue contour deficiencies, such as wrinkles and nasolabial folds. The product is non-bacterial, non-animal based, and not chemically cross-linked, which is intended to reduce the likelihood of allergic reactions. Although it received CE Mark approval and was launched in Europe in 2006, marketing and salesforce support were largely withdrawn by 2008.
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 Laresse.