Cimzia® was well tolerated and showed a favourable benefit-risk profile over the 26-week treatment period. Cimzia® was continued in 88% of patients beyond week 6 and in 67% beyond week 26. The adverse events were related to the active protein [32]. PEGASYS® (Pfizer) approved in 2002 is a PEGylated human interferon α-2a for the treatment of patients with chronic hepatitis C or chronic hepatitis B. Subcutaneous treatment is once per week for 48 weeks, and this cycle may be repeated. Toxicology studies

BMS-777607 datasheet included 4- and 13-week toxicity studies in monkeys; no chronic toxicity studies were conducted (FDA, EMA EPAR). Toxicity observed was characteristic to interferon α, and no PEG-related histological or other changes were observed in the toxicity studies [13]. PEGASYS® was cleared mainly via the liver, its target organ and the kidney excreted the metabolic products [33]. In a 14C labelling study, 51% of the total radioactivity dose was found in urine, and 9.6% in faeces Selleck PLX4720 within 14 days after dosing. Subcutaneous and iv doses gave similar results. The bioavailability after sc administration of PEGASYS® is 61–80% in humans. The clinical dose of PEGASYS® is 2.7 and 3.6 µg kg−1 week−1 for a 50 kg person. No PEG-related events were reported [18]. Literature reviews of preclinical findings with other PEGylated molecules have identified findings of organ specific vacuolation in animals, with several molecules

[12, 13]. Vacuolation was seen in the kidney with a PEG-20 kDa TNF-binding protein (chronic doses of 10 mg kg−1 in rats or acute doses of 20–40 mg kg−1), whereas the same anti-TNF protein bound to a 50 kDa PEG showed minimal or no effects [23]. Importantly, there were no changes in kidney function associated with these effects. PEGylated haemoglobin (MP4: dosed at 21 mL kg−1 body weight MCE公司 with 4.3 g dL−1 of PEG-haemoglobin containing several 5 kDa PEG per molecule haemoglobin) administered to monkeys induced vacuolation in liver, renal tubules and macrophages in the bone marrow, spleen and lymph nodes at the high PEG-dose with MP4 replacing approximately 30% of the monkey’s blood volume [22].

For PEGylated haemoglobin, these vacuolation findings were dose dependent, transient and without toxic effects [13]. Several PEGylated coagulation factors are currently in clinical development. The following briefly summarizes the relevant non-clinical and clinical safety information available from literature. GlycoPEGylated rFVIIa (N7-GP), which is manufactured by enzymatic mono-PEGylation (>85% mono-PEGylated) of N-linked carbohydrate structures on rFVIIa, results in a 40-kDa PEG moiety attached to the rFVIIa protein. To determine the safety and pharmacokinetics of a single doses of N7-GP in healthy men, a randomized, placebo-controlled, dose-escalation trial with five cohorts (N7-GP dose of 12.5–100 μg kg−1) was performed. In each cohort, eight subjects were randomized to receive N7-GP (n = 6) or placebo (n = 2).