Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Pegademase bovine is a modified form of the enzyme adenosine deaminase (ADA) derived from bovine sources and conjugated with polyethylene glycol (PEG) to extend its half-life in circulation. It is used as an enzyme replacement therapy for severe combined immunodeficiency disease (SCID) associated with ADA deficiency. The drug works by replacing the missing or deficient ADA enzyme, thereby reducing toxic levels of adenosine and 2'-deoxyadenosine that accumulate in patients with ADA deficiency and are harmful to lymphocytes. This correction helps restore immune function over time, although improvement may take weeks to months. Pegylation reduces immunogenicity and prolongs the duration of action[1][2][4][5][6][8].
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 pegademase bovine.