Rozrolimupab
| Clinical data | |
|---|---|
| ATC code | none |
| Identifiers | |
| |
| CAS Number |
909402-77-3  |
| ChemSpider | none |
| Chemical and physical data | |
| Molar mass | Antibodies 144.8–148.8 kg/mol |
 (what is this?) (verify) | |
Rozrolimupab is a recombinant antibody mixture, specifically containing 25 Rhesus D, or RhD, human antibodies, and is currently under development by Symphogen for the treatment of immune thrombocytopenic purpura (ITP) and for the prevention of hemolytic disease of the newborn (HDN). [1]
Clinical trials
Phase two trials have proved to be promising. Utilizing a single intravenous infusion dosing, this phase was held in 41 centers across the United States, Europe, and Asia in order to evaluate an effective dose.[1] The 61 patient study was assesing rozrolimupab's ability to effectively treat ITP and HDN as well as how safe and tolerable the drug is. Common adverse effects included mild to moderate headache, pyrexia, chills, and fatique. The study showed that administration of the drug did effect platelet responses in the blood, with a median time of response of roughly two and a half days, and on average lasting a total of 14 days.[2]
Current ITP and HDN treatment
While the current blood-derived treatment has proved successful, its dependence on a donor population proves problematic. Rozrolimupab's manufactured antibody mixture allows for a promising future.[1]
References
- 1 2 3 "Symphogen Rozrolimupab". Retrieved 2013-12-11.
- ↑ "Symphogen Pressroom". Retrieved 2013-12-11.