Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Megace ES (megestrol acetate) is an oral suspension formulation developed by Par Pharmaceutical that utilizes nanocrystal technology to enhance the bioavailability of megestrol acetate, a synthetic derivative of the steroid hormone progesterone. This 'Enhanced Solubility' (ES) version allows for a significantly lower volume of administration compared to the original Megace suspension. It is primarily indicated for the treatment of anorexia, cachexia, or unexplained significant weight loss in patients with acquired immunodeficiency syndrome (AIDS). Megestrol acetate acts as an appetite stimulant, likely through its activity as a progesterone receptor agonist and its ability to modulate hypothalamic neuropeptides (such as neuropeptide Y) and suppress pro-inflammatory cytokines like IL-1, IL-6, and TNF-alpha. It also possesses antineoplastic properties and is used in the management of advanced breast and endometrial cancers.
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 Megace ES.