Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The molybdenum cofactor (MoCo) is a vital component required for the proper functioning of molybdenum-dependent enzymes, including sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase. In Molybdenum Cofactor Deficiency (MoCD) Type A, the body is unable to synthesize this essential cofactor, leading to the accumulation of neurotoxic metabolites. As a therapeutic agent, the molybdenum cofactor would function as an enzyme cofactor replacement therapy, directly supplying the missing cofactor to restore the activity of these critical enzymes and mitigate the effects of the deficiency. The precursor to the molybdenum cofactor, cyclic pyranopterin monophosphate (cPMP), is administered as fosdenopterin (Nulibry) to enable the body to produce the active molybdenum cofactor.
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 Molybdenum Cofactor.