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Hemophilia A is a rare X-linked bleeding disorder caused by lack or dysfunction of coagulation factor VIII (FVIII). Hemophilia A is treated with replacement therapy, but frequent injections of the missing FVIII often lead to the formation of inhibitory antibodies. Patients who develop high levels of inhibitors must be treated with bypassing agents such as activated FVII (FVIIa). Both FVIII and FVIIa have short half-lives and require multiple injections. Long-acting forms of these proteins would therefore reduce the frequency of injections, improve patient compliance and reduce complications. In this article we present a new platform technology that produces long-acting forms of FVIII and FVIIa and improves the efficacy of hemophilia treatment. This technology is based on the binding of proteins/peptides to the outer surface of PEGylated liposomes (PEGLip). Binding is dependent on an amino acid consensus sequence within the proteins and is highly specific. At the same time, binding is non-covalent and does not require any modification of the therapeutic agent or its production process. Association of proteins with PEGLip results in substantial enhancements in their pharmacodynamic properties following administration. These improvements seem to arise from the association of formulated proteins with platelets prior to induction of coagulation.
Hemophilia is an inherited bleeding disorder caused by the lack or dysfunction of coagulation factors VIII (FVIII) or IX (FIX). The genes for FVIII and FIX are located on the X chromosome, and the vast majority of individuals with hemophilia are males. Hemophilia A accounts for approximately 75%–80% of all hemophilia cases with a prevalence of approximately 1/10,000 in the male population, whereas the prevalence of hemophilia B is 1/30,000.1,2 The severity of the bleeding tendency is determined by the residual clotting factor activity. Approximately 40% of hemophilia patients have a severe form of the disease, defined as having less than 1% (0.01 IU/ml) of normal factor activity.3
Hemophilia patients experience spontaneous hemorrhages into the joints, particularly the weight bearing joints such as knees, ankles and hips. This bleeding is painful and leads to long term inflammation and deterioration of the joint, resulting in permanent deformities, misalignment and loss of mobility. This is the major complication of hemophilia.4,5 Bleeding may also occur into the muscles, soft tissues and other organs.
Hemophilia is treated by supplying patients with the missing coagulation factor (FVIII or FIX). Replacement therapy may be provided on-demand (to stop a bleed) or prophylactically (to prevent bleeds). When treatment is provided on-demand, injections must be initiated at the first onset of symptoms so as to limit both the amount of bleeding and the extent of the resulting tissue damage.6 Prophylactic treatment has been shown to provide hemophilia patients with better overall care than on-demand treatment as it reduces the frequency of hemorrhages and slows the development of long term arthropathy.7 However, prophylactic treatment is more expensive than on-demand treatment and is not accessible to many patients.6
In this review, we focus on the treatment of hemophilia A, the most common form of the disease. The FVIII used to treat hemophilia A may be produced in mammalian cell lines genetically engineered to synthesize human FVIII (recombinant FVIII, rFVIII) or may be purified from normal pooled plasma (plasma-derived FVIII, pdFVIII).8
FVIII is a large glycoprotein (2332 amino acids) that is synthesized as a 330 kDa precursor and undergoes multiple processing steps to yield a heterodimer composed of a light chain (80 kDa) and a heterogeneous heavy chain (90–210 kDa)9 FVIII circulates in the plasma as an inactive precursor, tightly complexed with von Willebrand factor (vWF). Upon initiation of coagulation, FVIII is activated by thrombin. It dissociates from vWF, interacts with negatively charged phospholipids on the surface of activated platelets, and acts as a cofactor for factor IXa in the activation of factor X.1 This in turn leads to the generation of substantial amounts of thrombin, the key enzyme in the coagulation cascade, and to the generation of a hemostatic plug.
The half-life of human FVIII is about 10–12 hours.10,11 Effective prophylactic therapy therefore requires three weekly infusions of 20–40 IU/kg to maintain FVIII above levels at which spontaneous bleeding occurs.7 The need for frequent infusions reduces quality of life and may lead to problems with compliance and injection complications.12 Central venous access devices are frequently required, especially in children, but these devices are plagued by recurrent infections and thrombosis.13
Replacement treatment is complicated by the emergence of antibodies that inhibit the activity of the injected protein.14 Approximately 20%–40% of hemophilia A patients and 2%–3% of hemophilia B patients develop inhibitors.15,16 As expected, the more profound mutations resulting in the lack of circulating FVIII or FIX are associated with higher risk of inhibitor development.17 Neutralizing or inactivating autoantibodies to FVIII may also develop in patients without a history of coagulation factor deficiency. This condition, known as acquired hemophilia, affects 0.2–1 out of every million people per year.18 Despite the low incidence of acquired hemophilia, the disorder is often devastating and the costs of treatment are immense. There is therefore considerable interest in improving and optimizing existing treatment regimens.18,19
Treatment of hemophilia patients with inhibitors is based primarily on controlling or preventing acute hemorrhages and their sometimes life threatening complications. Patients with low inhibitor titers may be given high doses of factor concentrate. While some of the factor is neutralized by the inhibitors, enough remains in the circulation to induce hemostasis. Patients with high inhibitor titers (≥5 Bethasda units, BU) cannot be treated by replacement therapy because even high doses of coagulation factor are rapidly inactivated by the circulating antibodies.20 These patients must be treated with agents capable of inducing hemostasis independent of the presence of FVIII or FIX (bypassing agents). Two such agents are in widespread use: activated prothrombin complex concentrate (aPCC, also known as factor eight inhibitor bypass activity, FEIBA, Baxter AG, Vienna, Austria)21 and recombinant activated factor VII (rFVIIa; NovoSeven, Novo Nordisk AS, Bagsværd, Denmark).15,22 rFVIIa, given at supraphysiological doses, has been approved in many countries for the treatment of bleeding episodes in patients with congenital hemophilia and inhibitors to FVIII or FIX and patients with acquired hemophilia.23 The half-life of FVIIa in the circulation is approximately 2.3 hours.24,25 In most patients, bleeding episodes are therefore brought under control by administering two or three doses of 90 μg/kg given at two hour intervals.26,27
A long-acting form of FVIII would provide extended protection against bleeding and reduce gaps in protection caused by drops in FVIII levels between injections. Therefore, fewer injections would be required, resulting in fewer injection related complications, and better quality of life. Several attempts have been made to generate long-acting forms of FVIII.28 These included mutagenesis of the FVIII molecule to increase its stability29–31 and direct PEGylation of the FVIII protein.32–35 Modifying a large and complex protein such as FVIII is a difficult undertaking, though. The integrity of multiple active sites must be maintained and protein conformation must be preserved. Development of modified forms of FVIII is still in the preclinical stage and the safety and efficacy of these approaches has yet to be demonstrated in humans.28
There is also a clinical need for a more potent and long-acting form of FVIIa. As in the case of FVIII, long-acting FVIIa would require fewer injections, would reduce injection associated complications, and would provide patients with better control of bleeding episodes with fewer dips in FVIIa levels. Several approaches have been employed in attempts to improve FVIIa. These include substitution of one or more amino acids within the protein,36 PEGylation,37 and fusion of FVIIa to albumin.38 These proteins showed promising results in-vitro and in-animal models, but as in the case of FVIII, the efficacy and safety of these approaches has yet to be demonstrated in humans.
Liposomes, artificial phospholipid vesicles, have proven to be useful in stabilizing drugs and improving their pharmacological properties. In most cases, liposomes are used to encapsulate the therapeutic agent (usually a small molecule drug).39 Modifying the liposome surface with molecules such as polyethylene glycol prevents adsorption of plasma proteins to the liposome surface and interferes with recognition and uptake by the reticoloendothelial system (RES). This results in the generation of liposomes with a dramatically extended circulation time.40,41
PEGylated liposome (PEGLip) technology is a new approach to improving the pharmacodynamic properties of therapeutic proteins. Instead of encapsulating the drug, PEGylated liposomes are used as carriers with the protein bound non-covalently but with high specificity to the outer surface (Figure 1). Unlike approaches such as mutagenesis, direct PEGylation, or fusion to carrier proteins, PEGLip technology does not involve changes to a protein’s amino acid sequence and does not involve covalent attachment of stabilizing agents.
The PEGLip that we typically produce are composed of a 97:3 molar ratio of 1-palmitoyl-2-oleoyl phosphatidylcholine (POPC) to 1,2 distearoyl-sn-glycero-3-phosphatidylethanolamine-N-[methoxy(polyethyleneglycol)-2000] (DSPE-PEG 2000). The liposomes are prepared as follows. Lipids are dissolved in tert-butanol and lyophilized. The resulting dry lipid powder is resuspended to 110 mM lipid in 50 mM sodium citrate, pH 6.7 to form liposomes. The liposomes are then down-sized by extrusion through sequentially smaller polycarbonate filters until they reach a final diameter of 80–100 nm. The PEG molecules that extend outward from the liposome surface mediate binding of FVIII, FVIIa and other proteins to the liposome surface (Figure 1). As mentioned above, the PEG molecules also limit uptake of the liposomes by the RES, thereby extending half-life in the circulation.42–44
The binding of PEGLip to FVIII and FVIIa was demonstrated in real time using surface plasmon resonance (SPR). The protein being assayed was bound to the surface of a chip and association of liposomes was measured as a liposome solution flowed over the chip. SPR measurements showed that PEGLip bind both recombinant and plasma-derived FVIII45,46 as well as FVIIa.47 PEGLip also bind additional proteins such as recombinant human granulocyte colony-stimulating factor (G-CSF), granulocyte macrophage colony-stimulating factor (GM-CSF), and glucagon-like peptide 1 (GLP-1).48 Affinity constants (KD) for all of these interactions were in the low nM range (0.4–12 nM). All of the proteins that bind PEGLip share a consensus sequence of 8 amino acids (S/T–X–L/V–I/Q/S–S/T/Q–X–X–E) (Figure 1). A synthetic peptide derived from one of the two consensus sequences in FVIII (amino acids 1783–1796 of FVIII) also binds PEGLip with high affinity (KD of 2.3 nM). PEGLip do not bind several proteins that lack the consensus sequence, highlighting its significance for binding. These proteins include human serum albumin (HSA), human IgG, insulin, interferon alpha 2a, interferon alpha 2b, human growth hormone, and erythropoietin.48 Together, our data show that the consensus sequence is sufficient to mediate the binding of the proteins/peptides to PEGLip.
We also sought to identify the molecules or structure on PEGLip responsible for protein/peptide binding. We found that non-PEGylated POPC liposomes do not bind FVIII,45,46 FVIIa,47 or the FVIII-derived synthetic peptide.48 Analyses performed with liposomes composed of various types of lipids and lipid polymers revealed that the interaction between PEGLip and proteins is mediated primarily by the PEG molecule and the carbamate group adjacent to the PEG molecule within DSPE-PEG 2000.48 When PEG molecules were not present on the liposome surface (as in the case of POPC liposomes) no binding occurred. Likewise, when proteins lacking the consensus sequence were assayed, no binding was observed. Liposome-protein binding is therefore highly specific.
Formulation of a protein with PEGylated liposomes is very straightforward. The lyophilized protein powder of FVIII or FVIIa is simply reconstituted in liposome solution and allowed to fully dissolve. Even large and sensitive proteins such as FVIII may be formulated without any change in the production process or the purification procedure.45–47,49 Formulation is very gentle and it does not involve any covalent modification of the protein. The protein’s native structure is not changed, and the likelihood of antibody production does not increase. The protein is fully active immediately after formulation45–47 and it is free to interact with its normal binding partners.45 Administration to patients remains for the most part unchanged, though dosage and frequency of injections may need to be adjusted to account for extended therapeutic activity.
FVIII binds PEGLip specifically and with high affinity (two binding sites, KD of 4.5 and 1.9 nM), but this interaction does not alter FVIII activity, as shown by maintenance of full activity after formulation.45,46 The association of FVIII with PEGLip does not affect the FVIII protein’s structure. This was demonstrated by binding of several anti-FVIII antibodies to FVIII following PEGLip formulation45 Moreover, PEGLip formulation allows FVIII to interact with its natural binding partners. This was shown by in-vitro binding of PEGLip-formulated FVIII to vWF.45 Thus binding of PEGLip to FVIII does not change the protein’s biological properties.
PEGLip formulation of both recombinant and plasma–derived forms of FVIII extends hemostatic efficacy in vivo. This was demonstrated by better survival of hemophilic mice following tail-vein transection. Standard FVIII, PEGLip-FVIII, or saline were administered to hemophilic mice 24 hours prior to transection of the left lateral tail vein. Mice that received PEGLip-FVIII bled less and survived significantly longer (P < 0.05) than mice that received standard FVIII or saline (Figure 2A).45,46 This significantly increased survival of tail-vein transected hemophilic mice following the injection of PEGip formulated recombinant FVIII was also demonstrated by others.50 The increased survival rate was dependent on the pre-formation of a complex of FVIII and PEGLip. Clotting times of whole blood samples from hemophilic mice injected with PEGLip-FVIII were much shorter than the clotting times of blood samples from mice injected with free FVIII. This faster clotting was detected shortly after injection and at various time points up to 72 hours post injection.50
PEGLip-FVIII provides human subjects with extended protection from bleeding.49 Several clinical trials tested the safety and the efficacy of PEGLip rFVIII (also referred to as BAY 79-4980).51 A single arm, subject blinded clinical trial was performed to assess the efficacy and safety of two levels of FVIII (25 or 35 IU/kg) with a fixed dose of liposomes (22 mg lipids/kg). Twenty-three severe hemophilia A patients were treated in three study segments. Standard FVIII was administered in the first study segment whereas PEGLip-FVIII was provided in the second and third segments. Segments were separated by 4-day washout periods and each prophylactic infusion was administered while subjects were in a non-bleeding state. As a measure of efficacy, the time between each prophylactic infusion and the next spontaneous bleed was recorded. Prophylactic treatment with PEGLip-FVIII nearly doubled the length of time subjects were protected from spontaneous bleeding (Figure 2B). A single prophylactic injection of 25 IU/kg PEGLip-FVIII resulted in a mean bleed-free interval of 10.9 days compared to 5.9 days with standard FVIII. Similarly, injection of 35 IU/kg PEGLip-FVIII resulted in a mean bleed-free interval of 13.3 days compared to 7.2 days with standard FVIII. This difference was significant (P < 0.05) for both dose levels (Figure 2B).49
A subsequent randomized, subject blinded, four-way crossover study involving 16 hemophilia A patients evaluated the efficacy and safety of prophylactic infusions of various PEGLip doses (4.2, 12.6, or 22.1 mg/kg) with a fixed FVIII dose (35 IU/kg). Mean number of bleeding-free days after each infusion increased from 7.8 days for 35 IU/ml of standard FVIII to 8.7, 10.8, and 10.9 days for 35 IU/ml of FVIII formulated in 4.2, 12.6, and 22.1 mg/kg of PEGLip, respectively.52 The study showed a dose response to PEGLip that reached saturation at the highest dose level.
An additional study tested the safety of PEGLip-FVIII and compared its pharmacokinetic profile to that of standard FVIII.53 In this randomized double-blind study, 26 severe hemophilia A patients received a single injection of standard FVIII (35 IU/kg) followed by 12 observation days and a 4-day Washout period. Patients then received a single injection of PEGLip-FVIII (35 IU/kg FVIII, 13 or 22 mg/kg PEGLip) followed once again by 12 days of observation. Pharmacokinetic (PK) analysis based on samples taken from patients during the trial showed no significant difference between standard FVIII and PEGLip-FVIII. This suggests that the increased protection from bleeding observed with PEGLip-FVIII did not result from a simple prolongation of FVIII half-life in the blood stream.
Safety and tolerability of PEGLip-FVIII were assessed in another clinical trial involving 18 severe hemophilia A patients. This study was directed primarily at determining the optimal infusion rate for PEGLip-FVIII. The study showed that PEGLip-FVIII may be administered at an infusion rate similar to that of standard FVIII.54
In all four of the studies described above, no production of inhibitory antibodies was detected, and no serious adverse events were reported. However, a few subjects experienced increased breathing frequency and flushing.53,54 At the first sign of symptoms, infusions were stopped and the patients recovered fully without further medical intervention. This type of hypersensitivity reaction is known as complement activation related pseudoallergy (CARPA) and has been described following administration of radiocontrast media, liposomal drugs, and micellar solvents. Unlike IgE mediated reactions, CARPA reactions arise at first treatment and become milder or disappear upon repeated exposure.54,55
The combined results of the phase I and II clinical studies described above show that PEGLip-FVIII is well tolerated and provides extended protection from bleeding following prophylactic treatment.
PEGLip formulation is desirable for FVIIa because this therapeutic protein has an extremely short half-life in the circulation (approximately 2.3 hours).24,25 In most patients treated with FVIIa, effective hemostasis is achieved only after two or three doses of 90 μg/kg26,27 given at two hour intervals.
SPR analyses showed that PEGLip bind specifically to FVIIa. As in the case of FVIII, binding of liposomes to FVIIa was dependant on the presence of the DSPE-PEG lipopolymer. POPC liposomes lacking DSPE-PEG bound FVIIa to a much lower level than PEGLip. Kinetic analysis of the PEGLip-FVIIa interaction indicated that the PEGLip bind to FVIIa with an affinity (KD) of 0.4 nM.47 Formulation of FVIIa with PEGLip did not affect its in vitro activity.47 Most importantly, formulation of FVIIa with PEGLip improved survival of hemophilic mice following tail vein transection. Hemophilic mice were injected with standard FVIIa, PEGLip-FVIIa, or saline. Fifteen minutes after injection, tail veins were transected and survival was scored up to 24 hours. We found that mice injected with PEGLip-FVIIa survived significantly longer (P < 0.05) than mice injected with standard FVIIa (Figure 3A).
The safety and efficacy of PEGLip-FVIIa were tested in humans in an open label, exploratory, cross over, phase I/II clinical study in six adult subjects with severe hemophilia A and inhibitory FVIII antibodies.56 Each subject received two infusions: one infusion of 90 μg/kg standard FVIIa and one infusion of 90 μg/kg PEGLip-formulated FVIIa. The two infusions were separated by a 10-day washout period. Injection volume was kept constant while injection order was randomized. Blood samples were collected from patients at various time points both before and after each infusion of FVIIa or PEGLip-FVIIa. Whole blood samples were then analyzed by rotational thrombelastography, a method recording the kinetics of clot formation and the firmness of the clots. PEGLip-formulated FVIIa produced significantly (P < 0.05) shorter clotting times and higher clot firmness than standard FVIIa up to 5 hours post injection. Clotting time of standard FVIIa 30 min post injection was the same as clotting time of PEGLip-FVIIa 2 hours post injection. Clotting time of standard FVIIa 1 hour post injection was the same as clotting time of PEGLip-FVIIa 3.2 hours post injection (Figure 3B). Maximal clot firmness induced by standard FVIIa 0.5 hour post injection was as high as that induced by PEGLip-FVIIa ~2.7 hours post injection. Thrombin generation assays showed that thrombin was produced faster and more efficiently following infusion of PEGLip-FVIIa than following infusion of standard FVIIa. No significant differences were detected between the PK of PEGLip-FVIIa and standard FVIIa.
One of the subjects in the trial experienced transient hyperemia, an increase in blood pressure and anxiety during the infusion of the first 1 mL of PEGLip-FVIIa. This non-IgE mediated reaction (CARPA) is associated with PEGLip.55 and is not related to FVIIa. The reaction subsided within one hour. In all other subjects, PEGLip-FVIIa was well tolerated and there were no serious adverse events nor were there any significant changes in vital signs, clinical chemistry or hematological parameters. Measurements of coagulation parameters indicated that there was no increase in thrombotic risk.
An analysis of the results of the clinical trial indicates that PEGLip-FVIIa provides about two more “efficacy hours” than standard FVIIa. In treatment of bleeding episodes in hemophilia patients with inhibitors, one 90 μg/kg dose of PEGLip-FVIIa may be roughly equivalent to two infusions of standard FVIIa given at 2-hour intervals.
In preclinical models, formulation of FVIII and FVIIa with PEGLip improved pharmacokinetic properties in vivo and increased circulation half-life.45–47 However, phase I clinical experiments showed that there was no difference between the pharmacokinetic behavior of standard FVIII and PEGLip-formulated FVIII53 and between standard FVIIa and PEGLip-formulated FVIIa.56 This suggests that extension of circulation half-life is not the primary mechanism responsible for increased hemostatic efficacy.
Extensive in vitro experiments measuring clot formation and lysis by rotational thrombelastography, indicate that platelets must be present in order for PEGLip formulation to improve the hemostatic properties of FVIII and FVIIa.47,57 When PEGLip-FVIII and PEGLip-FVIIa were added to severe hemophilic whole blood or platelet rich plasma, clots formed much faster than when similar concentrations of standard FVIII and FVIIa were used. Clots were also firmer and more resistant to fibrinolysis. Similarly, ex-vivo rotational thrombelastometry experiments in whole blood drawn from hemophilic mice indicated that clotting times were much faster in mice injected with PEGLip-FVIII rather than with free FVIII.50 Such improvements in kinetics, clot firmness, and resistance to fibrinolysis depended on platelets as they were not observed when experiments were performed in platelet poor plasma.57
In order to gain a deeper understanding of the mechanisms responsible for these improvements in efficacy, we tested whether PEGLip themselves bind platelets. Flow cytometry analysis indicated that fluorescent PEGLip associate with platelets in-vitro in a dose related manner. This association was further confirmed in-vivo following the injection of fluorescent PEGLip into hemophilic mice.57 Interactions between liposomes of various compositions, including PEG liposomes, and blood cells have been reported previously by others.50,58
Having shown that PEGLip bind FVIII and FVIIa45,47 and that PEGLip bind platelets, we next tested whether PEGLip are capable of delivering proteins to platelets. Fluorescently labeled FVIII and FVIIa were formulated with non-fluorescent PEGLip and shown by flow cytometry to bind human platelets in-vitro. These results were also found in-vivo as PEGLip-formulated fluorescent proteins interacted with the platelets of hemophilic mice following injection.57 Fluorescently labeled human serum albumin (HSA), which does not bind to PEGLip, did not show increased binding to platelets following formulation with PEGLip. This indicates that PEGLip-mediated association of proteins with platelets is dependent on prior binding of the proteins to PEGLip.
The combined results indicate the following mechanism (Figure 4): Formulation of FVIII or FVIIa with PEGLip leads to non-covalent binding of the protein to the outer surface of the PEGylated liposomes. After injection of the formulated proteins to the bloodstream the liposomes associate with non-activated platelets and a complex of platelet-PEGLip-protein (FVIII/FVIIa) is formed in-vivo. Following injury, platelets are recruited to sites of injury where they adhere to the damaged vessel wall. Due to their prior association with PEGLip, they carry FVIII and FVIIa with them. Platelets are activated at the wound site and coagulation complexes form on the surface of the activated platelets. Since FVIII and FVIIa are already present on the platelets prior to activation, the coagulation cascade is more efficient. Clots form faster and the clots are more stable.
The association of PEGLip-FVIII or PEGLip-FVIIa with platelets may also lead to increased concentration of FVIII or FVIIa at the wound site, even when the overall concentration of FVIII or FVIIa in the circulation is low. Accordingly, expression of FVIII in platelets was shown to be effective at inducing hemostasis even when FVIII protein expression levels did not exceed 1% of normal levels. This was probably due to recruitment of platelets to the sites of injury and local release of FVIII from activated platelets at wound sites.59
PEGLip technology improves the pharmacodynamic properties of both coagulation factors VIII and VIIa. This was demonstrated in preclinical experiments and in five different clinical trials with both FVIII and FVIIa. The combined results indicate that PEGLip-FVIII prevents bleeding for a significantly longer period than standard FVIII, and that one dose of PEGLip-FVIIa may be roughly equivalent to two infusions of standard FVIIa given at 2 hour intervals when treating a bleed in hemophilia patients with inhibitors.
Of the approaches currently available to generate long-acting forms of FVIII and FVIIa, PEGLip formulation has the advantage of being the only approach that has been tested extensively in clinical trials. PEGLip-FVIII and PEGLip-FVIIa have been shown to be safe in trials involving more than 90 hemophilia patients. In general, treatments with PEGLip-formulated FVIII and FVIIa were well tolerated.
One of the most problematic complications of hemophilia treatment is the induction of inhibitory antibodies. PEGLip formulation does not change the structure of FVIII and FVIIa. It thereby avoids one of the biggest obstacles to producing improved coagulation factors: changes in structure that induce antibody formation. Because of the large size and complexity of the FVIII protein and the sensitivity of hemophilia A patients to even small changes in the protein,60,61 FVIII can be considered a worst case scenario for increased immunogenicity. Extensive experience with PEGLip-FVIII in several clinical studies has shown no increase in antibody generation. PEGLip formulation thus avoids one of the major pitfalls of the drug development process.49,52,53
PEGLip-FVIII/FVIIa are well tolerated and suitable for long-term treatment of hemophilia. This was demonstrated in toxicology studies, which included injecting high doses of PEGLip-FVIII and PEGip-FVIIa into rats and rabbits (acute toxicology) and repeated injections (up to nine months of weekly injections) of PEGLip into rats and rabbits.45 PEGylated liposomes were also shown to be non-toxic in mice and dogs.62
In the years to come, we expect PEGLip-FVIII and PEGLip-FVIIa to become an attractive treatment for hemophilia A patients and hemophilia patients with inhibitors.
The authors are employees of Omri Laboratories Ltd. The authors report no conflicts of interest in this work.