Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Recombinant human apolipoprotein M (rhAPOM) is a recombinant version of the human apolipoprotein M (ApoM) protein, a 25 kDa member of the lipocalin protein superfamily. ApoM is primarily expressed in the liver and kidneys and serves as the principal physiological carrier of the bioactive lipid sphingosine-1-phosphate (S1P) in high-density lipoprotein (HDL) particles. Developed by the University of Miami Miller School of Medicine in collaboration with Pfizer's Centers for Therapeutic Innovation, rhAPOM is being investigated as a systemic replacement therapy for glomerular diseases, specifically Alport syndrome. In preclinical models of Alport syndrome (Col4a3 knockout mice), weekly administration of rhAPOM restores renal ApoM levels, reduces triglyceride and lipid droplet accumulation in podocytes by promoting cholesterol efflux, and protects against renal failure, albuminuria, glomerulosclerosis, and tubulointerstitial fibrosis.
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 recombinant human apolipoprotein M.