Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Fensolvi is a branded, long-acting injectable formulation of leuprolide acetate, a synthetic nonapeptide analog of naturally occurring gonadotropin-releasing hormone (GnRH). It acts as a GnRH agonist and is indicated for the treatment of pediatric patients 2 years of age and older with central precocious puberty (CPP). Fensolvi utilizes an innovative in-situ polymeric gel delivery system that allows for sustained release over six months following subcutaneous injection. By continuously stimulating pituitary GnRH receptors, it initially increases and then suppresses luteinizing hormone (LH) and follicle-stimulating hormone (FSH) secretion, leading to decreased production of sex steroids from the gonads. This mechanism halts or reverses premature pubertal development in affected children. The drug was developed by Tolmar Pharmaceuticals[3][4][5][10].
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 fensolvi.