Eculizumab, the active ingredient in Soliris, is a monoclonal antibody that specifically binds to the complement protein C5 with
high affinity, thereby inhibiting its cleavage to C5a and C5b and
preventing the generation of the terminal complement complex C5b-9.
Soliris inhibits terminal complement mediated intravascular hemolysis
in PNH patients. [emphasis mine]
A genetic mutation
in PNH patients leads to the generation of populations of abnormal RBCs
(known as PNH cells) that are deficient in terminal complement
inhibitors, rendering PNH RBCs sensitive to persistent terminal
complement-mediated destruction. The destruction and loss of these PNH
cells (intravascular hemolysis) results in low RBC
counts (anemia),
and also fatigue, difficulty in functioning, pain, dark urine,
shortness of breath, and blood clots.
In the placebo-controlled clinical study, Soliris when administered as recommended
reduced hemolysis as shown by the reduction of serum
LDH
levels from 2200 ±
1034 U/L (mean ± SD) at baseline to 700 ± 388 U/L by week one
and maintained the effect through the end of the study at week 26 (327
±
433 U/L). In the single arm clinical study, Soliris maintained this
effect through
52 weeks [see CLINICAL STUDIES].
A population PK analysis with a standard 1-compartmental model was conducted
on the multiple dose PK data from 40 PNH patients receiving the
recommended
Soliris regimen [see DOSAGE AND ADMINISTRATION].
In this model, the clearance of Soliris for a typical PNH patient
weighing 70
kg was 22 mL/hr and the volume of distribution was 7.7 L. The
half-life was
272 ± 82 hrs (mean ± SD). The mean observed peak and trough serum
concentrations of Soliris by week 26 were 194 ± 76 mcg/mL and 97 ±
60 mcg/mL, respectively.
Studies have not been conducted to evaluate the PK of Soliris in special patient populations identified by gender, race, age (pediatric
or geriatric), or the presence of renal
or hepatic
impairment.
Tags:
Permalink Reply by Linda Burke on April 6, 2010 at 10:36pm
Permalink Reply by Joy Lewis O'Brien on April 7, 2010 at 7:01pm Thanks, Joy - I appreciate you adding this very specific information on Soliris. As we discussed, it's been the best and most detailed info I've found anywhere. If someone else has additional information, we'd certainly welcome it!
Permalink Reply by Cheryl Biermann on April 8, 2010 at 9:05am WELCOME - Friends, Family Members, Patients, and Researchers - JOIN US!
The Foundation for Children with Atypical HUS encourages patients and investigators to share information and explore options/resources as we work together to gain insight into this rare complement disorder. By increasing contact opportunities with researchers and medical personnel interested in helping the aHUS community, our stories foster a better understanding of atypical hemolytic uremic syndrome.
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