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WILATE, von Willebrand Factor/Coagulation Factor VIII
Complex
(Human)
WILATE is a human plasma-derived, sterile, purified, double virus inactivated von Willebrand Factor/Coagulation Factor VIII Complex. WILATE is supplied as a lyophilized powder for reconstitution for intravenous injection. The diluent for reconstitution of the lyophilized powder is Water for Injection with 0.1% Polysorbate 80.
WILATE contains no preservative. No albumin is added as a stabilizer. WILATE is labeled with the actual VWF:RCo and FVIII activities in IU per vial. The VWF activity (VWF:RCo) is determined using a manual agglutination method referenced to the current “WHO International Standard for von Willebrand Factor Concentrate”. The FVIII activity is determined using a chromogenic substrate assay referenced to the current “WHO International Standard for Human Coagulation Factor VIII Concentrate”. The assay methodologies are according to European Pharmacopoeia (Ph.Eur.). The resulting specific activity of WILATE is ≥ 60 IU VWF:RCo and ≥ 60 IU FVIII activities per mg of total protein.
The nominal composition of WILATE is as follows:
| Component | Ouantity/ 5 mL vial | Ouantity/ 10 mL vial |
| VWF:RCo | 500 IU | 1000 IU |
| FVIII | 500 IU | 1000 IU |
| Total protein | ≤ 7.5 mg | ≤ 15.0 mg |
| Glycine | 50 mg | 100 mg |
| Sucrose | 50 mg | 100 mg |
| Sodium chloride | 117 mg | 234 mg |
| Sodium citrate | 14.7 mg | 29.4 mg |
| Calcium chloride | 0.8 mg | 1.5 mg |
| Water for injection | 5 mL | 10 mL |
| Polysorbate 80 | 1 mg/mL | 1 mg/mL |
Von Willebrand Factor/Coagulation Factor VIII complex is the active ingredient in WILATE. It is derived from large pools of human plasma collected in U.S. plasma donation centers. All plasma donations are tested for viral markers in compliance with requirements of EU CPMP and FDA guidance. In addition, the limit for the titer of human parvovirus B19 DNA in the manufacturing pool is set not to exceed 104 IU/mL.
The product is manufactured from cryoprecipitate, which is reconstituted in a buffer and treated with aluminum hydroxide followed by two different chromatography steps, ultra- and diafiltration, and sterile filtration. The manufacturing process includes two virus inactivation steps, namely, treatment with an organic solvent/detergent (S/D) mixture, composed of tri-n-butyl phosphate (TNBP) and Octoxynol-9, and a terminal dry heat (TDH) treatment of the lyophilized product in final container [at +100°C (212°F) for 120 minutes at a specified residual moisture level of 0.7-1.6%]. In addition, the ion-exchange chromatography step utilized during WILATE manufacturing also removes some viruses [8]. The mean cumulative virus reduction factors of these steps are summarized in Table 3.
Table 3 : Virus Reduction During WILATE Manufacturing
| Production Step | Virus Reduction Factor [loa10] | ||||||
| Enveloped Viruses | Non-Enveloped Viruses | ||||||
| S/D Treatment | HIV-1 > 7.52 | SBV > 8.63 | BVDV > 4.18 | PRV > 8.54 | REO 3 na | HAV na | PPV na |
| Ion-Exchange Chromatography | nd | nd | nd | nd | 1.86 -2.33 | 1.16 -1.93 | 3.29 |
| TDH Treatment | 4.91- > 5.79 | > 5.51 | nd | 3.99-4.87 | > 6.40 | > 5.69 | 2.57-4.12 |
| Global Reduction Factor | > 12.43- > 13.31 | > 14.14 | > 4.18 | > 12.53 - > 13.41 | > 8.26- > 8.73 | > 6.85- > 7.62 | 5.86-7.41 |
| na: not applicable nd: not done (S/D reagents present) HIV-1: Human Immunodeficiency Virus - 1 SBV: Sindbis Virus BVDV: Bovine Viral Diarrhea Virus PRV: Pseudorabies Virus REO 3: Reovirus Type 3 HAV: Hepatitis A Virus PPV: Porcine Parvovirus |
|||||||
REFERENCES
8. Stadler M., et al. Characterisation of a novel high-purity, double virus inactivated von Willebrand Factor and Factor VIII concentrate (Wilate). Biologicals 2006; 34:281-288
WILATE is indicated in children and adults with von Willebrand disease for:
WILATE is not indicated for the treatment of hemophilia A.
Required IU = body weight (kg) x desired VWF:RCo rise (%) (IU/dL) x 0.5 (IU/kg per IU/dL)
Epected VWF:RCo rise (% of normal) = 2 x administered IU/ body weight (kg)
A guide for dosing in the treatment of major and minor hemorrhages is provided in Table 1.
Table 1 : Dosing for
Treatment of Minor and Major Hemorrhages in all VWD types
| Type of Hemorrhages | VWF:RCo and FVIII Activity Trough Levels (% of normal) | Loading Dosage (IU VWF:RCo/kg body weight) | Maintenance Dosage (IU VWF:RCo/kg body weight) | Frequency of Doses (hours) | Duration of Therapy (days) |
| Minor | > 30 | 20-40 | 20-30 | Repeat as needed 12-24 | Up to 3 days |
| Major | > 50 | 40-60 | 20-40 | Repeat as needed 12-24 | Up to 5-7 days |
A guide for dosing in minor and major surgeries is provided in Table 2.
Table 2 : Dosing for
Treatment in Minor and Major Surgeries in all VWD Types
| Type of Surgery | Loading Dosage (IU VWF:RCo/kg body weight) (within 3 hours before surgery) | VWF:RCo Peak Levels (% of normal) | Maintenance Dosage (IU VWF:RCo/kg body weight) | VWF:RCo Trough Levels (% of normal) | Frequency of Doses (hours) | Duration of Therapy (days) |
| Minor (including tooth extraction) | 30-60 | 50 | 15-30 or half the loading dose | > 30 | 12-24 | Until wound healing achieved, up to 3 days |
| Major | 40-60 | 100 | 20-40 or half the loading dose | > 50 | 12-24 (at least 2 doses within first 24 hours after the start of surgery) | Until wound healing achieved, up to 6 days or more |
In order to decrease the risk of perioperative thrombosis, FVIII activity levels should not exceed 250%.
Whereas table 2 provides a dosing range that is expected to provide the desired peak levels of VWF:RCo, the following is an example on how to calculate the loading dose based on a patient's individual IVR which is to be determined pre-surgery.
Example:
Assumption: Baseline VWF:RCo value = 10 IU/dL, and VWF:RCo target level = 100 IU/dL = Δ 90 IU/dL
Assumption: Patient's weight = 75 kg, patient's IVR = 1.8 (IU/dL)/(IU/kg)
Loading Dose = 90 IU/dL x 75 kg /1.8 (IU/dL)/(IU/kg) = 3,750 IU VWF:RCo
1) Warm the concentrate (WILATE) and Diluent in the closed vials up to room temperature. If a water bath is used for warming, avoid water contact with the rubber stoppers or the caps of the vials. The temperature of the water bath should not exceed +37°C (98°F).
2) Remove the caps from the concentrate (WILATE) vial and the diluent vial and clean the rubber stoppers with an alcohol swab.
3) Peel away the lid of the outer package of the Mix2Vial™ transfer set. To maintain sterility, leave the Mix2Vial™ device in the clear outer packaging. Place the diluent vial on a level surface and hold the vial firmly. Take the Mix2Vial™ in its outer package and invert it over the diluent vial. Push the blue plastic cannula of the Mix2Vial™ firmly through the rubber stopper of the diluent vial (Fig. 1). While holding onto the diluent vial, remove the outer package from the Mix2Vial™, leaving the Mix2Vial™ attached firmly to the diluent vial (Fig. 2).
Figure 1 and 2
 |
4) With the concentrate (WILATE) vial held firmly on a level surface, quickly invert the diluent vial with the Mix2Vial™ attached and push the transparent plastic cannula end of the Mix2Vial™ firmly through the stopper of the concentrate (WILATE) vial (Fig. 3). The diluent will be drawn into the concentrate (WILATE) vial by the vacuum.
Figure 3
 |
5) With both vials still attached, gently swirl the concentrate (WILATE) vial to ensure the powder is fully dissolved to a clear solution. Do not shake the vial in order to avoid foaming. Once the contents of the WILATE vial are completely dissolved, firmly hold both the transparent and blue parts of the Mix2Vial™. Unscrew the Mix2Vial™ into two separate pieces (Fig. 4) and discard the empty diluent vial and the blue part of the Mix2Vial™.
The final solution is clear or slightly opalescent, colorless or slightly yellow. If the concentrate fails to dissolve completely or an aggregate is formed, do not use the preparation.
Figure 4
 |
For intravenous injection after reconstitution only
WILATE is available as a sterile, lyophilized powder for reconstitution for intravenous injection, provided in the following nominal strengths per single-use vial:
| Kit NDC Number | Size | Protein Amount |
| 68982-182-01 | 500 IU VWF:RCo and 500 IU FVIII activities in 5 mL | ≤ 7.5 mg |
| 68982-182-02 | 1000 IU VWF:RCo and 1000 IU FVIII activities in 10 mL | ≤ 15.0 mg |
REFERENCES
2. Nichols WL, Hultin MB, et al. von Willebrand Disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia 2008; 14: 171-232
4. Mannucci P.M., Federici A.B.: Antibodies to von Willebrand factor in von Willebrand disease; in Aledort L.M. (ed): Inhibitors to Coagulation Factors. New York, Plenum Press, 1995, pp 87-92
7. Azzi A., Morfini M., Mannucci P.M.: The transfusion-associated transmission of parvovirus B19. Transfus.Med.Rev. 1999;13:194-204
Manufactured by : Octapharma Pharmazeutika Produktionsges.m.b.H., Oberlaaer Strasse 235, A-1100 Vienna, Austria, U.S. License No. 1646. Distributed by : Octapharma USA, Inc., 121 River Street, 12th floor, Hoboken, NJ 07030, wilate® is a registered trademark of Octapharma. Issued August 2015
The most common adverse reactions to treatment with WILATE ( ≥ 1%) in patients with VWD were hypersensitivity reactions, urticaria, and dizziness. Seroconversions for antibodies to parvovirus B19 not accompanied by clinical signs of disease have been observed.
The most serious adverse reactions to treatment with WILATE in patients with VWD were hypersensitivity reactions [see WARNINGS AND PRECAUTIONS].
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed during these trials cannot be directly compared to rates in clinical trials of another drug and may not reflect the rates observed in clinical practice.
A total of 157 VWD subjects (aged 1 to 83 years) received WILATE on 6769 occasions, including clinical studies that involved prophylactic use, treatment on demand, surgery, and pharmacokinetics. Of the 157 subjects, 32 (20.4%) had VWD type 1, 42 (26.8%) had VWD type 2, and 83 (52.9%) had VWD type 3; 96 (61.1%) subjects were female and 61 (38.9%) subjects were male. Overall, subjects received 11,222,241 IU of WILATE during 6355 exposure days. The most common adverse reactions were hypersensitivity reactions (3 subjects; 1.9%), urticaria and dizziness (each with 2 subjects; 1.3%). Five subjects (3.2%) showed seroconversion for antibodies to parvovirus B19 not accompanied by clinical signs of disease. Seroconversion for parvovirus B19 DNA has not been reported since implementation of minipool testing of plasma used for the manufacture of WILATE.
The immunogenicity of WILATE was specifically assessed in 97 subjects in 3 clinical studies in which subjects received 9,635,041 IU of WILATE during 5575 exposure days. No inhibitors of VWF were detected in these 3 studies. In one of 3 studies, which also assessed FVIII inhibitor development in 15 subjects, no inhibitors of FVIII were detected after administration of a total of 223,290 IU of WILATE over 419 administrations.
The detection of antibody formation is highly dependent on the sensitivity and specificity of the assay. Additionally, the observed incidence of antibody (including neutralizing antibody) positivity in an assay may be influenced by several factors including assay methodology, sample handling, timing of sample collection, concomitant medications, and underlying disease. For these reasons, comparison of the incidence of antibodies to WILATE with the incidence of antibodies to other products may be misleading.
The following adverse reactions have been identified during the post-approval use of WILATE. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to product exposure.
Post-marketing adverse reactions reported in patients treated with WILATE include, dyspnea, nausea, vomiting, rash, headache, tachycardia, flushing, hypotension, chills, cough, chest discomfort, abdominal pain, pyrexia, factor VIII inhibition, anaphylactic reaction and paresthesia.
No information provided.
Included as part of the PRECAUTIONS section.
Hypersensitivity reactions may occur with WILATE. Signs and symptoms include angioedema, burning and stinging at the infusion site, chills, flushing, generalized urticaria, headache, hives, hypotension, lethargy, nausea, restlessness, tachycardia, tightness of the chest, tingling, vomiting, and wheezing that may progress to severe anaphylaxis (including shock) with or without fever.[3] Closely monitor patients receiving WILATE and observe for any symptoms throughout the infusion period.
Because inhibitor antibodies may occur concomitantly with anaphylactic reactions, evaluate patients experiencing an anaphylactic reaction for the presence of inhibitors.[3] [See Neutralizing Antibodies]
Continued treatment using a FVIII-containing VWF product may cause an excessive rise in FVIII activity[1], which may increase the risk of thromboembolic events. Monitor plasma levels of VWF:RCo and FVIII activities in patients receiving WILATE to avoid sustained excessive VWF and FVIII activity levels.
Neutralizing antibodies (inhibitors) to FVIII and VWF in patients with VWD, especially type 3 patients, may occur. If a patient develops inhibitor to VWF (or to FVIII), the condition will manifest itself as an inadequate clinical response. Thus, if expected VWF activity plasma levels are not attained, or if bleeding is not controlled with an adequate dose or repeated dosing, perform an appropriate assay to determine whether a VWF inhibitor is present.
In patients with antibodies against VWF, VWF is not effective and WILATE administration may lead to severe adverse events. Consider other therapeutic options for such patients.
Because inhibitor antibodies may occur concomitantly with anaphylactic reactions, evaluate patients experiencing an anaphylactic reaction for the presence of inhibitors.[3] [See Hypersensitivity Reactions]
WILATE is made from human plasma. Because this product is made from human blood, it may carry a risk of transmitting infectious agents, e.g., viruses, and theoretically, the variant Creutzfeldt-Jakob disease (vCJD) agent. There is also the possibility that unknown infectious agents may be present in the product. The risk that WILATE will transmit viruses has been reduced by screening plasma donors for prior exposure to certain viruses, by testing for the presence of certain current virus infections, and by inactivating and removing certain viruses during manufacture. Despite these measures, it may still potentially transmit disease. [5]
Record the batch number of the product every time WILATE is administered to a patient, and consider appropriate vaccination (against hepatitis A and B virus) of patients in regular/repeated receipt of WILATE. ALL infections thought by a physician possibly to have been transmitted by this product should be reported by the physician or other healthcare provider to Octapharma USA, Inc., at 1-866-766-4860.
REFERENCES
1. Mannucci P.M.: Venous thromboembolism in von Willebrand disease. Thromb Haemost 2002;88:378-379
3. Mollison.P.L., Engelfriet C.P., Contreras M.: Some unfavourable effects of transfusion; in Klein H.G., Anstee D.J. (eds): Mollison's Blood Transfusion in Clinical Medicine. Blackwell Publishing, 2005, pp 666-700
5. Kasper, C.K., Kipnis, S.A. Hepatitis and Clotting Factor Concentrates. JAMA1972; 221:510
6. Biggs, R. Jaundice and Antibodies Directed Against Factors VIII and IX in Patients Treated for Haemophilia or Christmas Disease in the United Kingdom. Br J Haematol 1974; 26:313-329
There is no data with WILATE use in pregnant women to inform a drug-associated risk. Animal reproduction studies have not been conducted with WILATE. WILATE was given to four subjects (3 type 3 and 1 type 2B) during labor and delivery in one clinical study. Two subjects underwent vaginal delivery (type 3) and two subjects had a cesarean section (type 3/type 2B). In this study all procedures were uneventful.
In the U.S. general population, regardless of drug exposure, the estimated background risk of major birth defect and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively.
There is no information regarding the presence of WILATE in human milk, the effect on the breastfed infant, and the effects on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for WILATE and any potential adverse effects on the breastfed infant from WILATE or from the underlying maternal condition.
Eleven pediatric subjects with VWD between 5 to 16 years of age (8 type 3, 1 type 2, 2 type 1) were treated with WILATE for 234 bleeding episodes (BEs) in clinical studies. Treatment success was achieved in 88% of BEs [see Clinical Studies]. Efficacy data during surgical prophylaxis were available for 13 pediatric VWD surgery subjects (3 subjects aged 0 to 2 years, 4 subjects aged 2 to 5 years, 3 subjects aged 6 to 12 years, and 3 subjects aged 12 to 16 years). Treatment success was achieved in 22 of 22 surgical procedures (17 minor and 5 major).
No dose adjustment is needed for pediatric patients as administered dosages were similar to those used in the adult population [see Clinical Trials].
Although some of the subjects who participated in the WILATE studies were over 65 years of age, the number of subjects was inadequate to allow subgroup analysis to support recommendations in the geriatric population.
No information provided.
WILATE is contraindicated in patients with known hypersensitivity reactions, including anaphylactic or severe systemic reactions, to human plasma-derived products, any ingredient in the formulation [see DESCRIPTION], or components of the container.
WILATE contains von Willebrand factor (VWF) and coagulation factor VIII (FVIII), constituents of normal plasma. VWF promotes platelet aggregation and platelet adhesion on damaged vascular endothelium; it also serves as a stabilizing carrier protein for the procoagulant protein FVIII, an essential cofactor in activation of factor X leading to formation of thrombin and fibrin. Patients suffering from VWD have a deficiency or abnormality of VWF. This reduction in VWF plasma concentration results in correspondingly low FVIII activity and abnormal platelet function, thereby resulting in excessive bleeding. [9] After administration, WILATE temporarily replaces missing VWF and FVIII that are needed for effective hemostasis.
There have been no specific pharmacodynamic studies on WILATE.
Pharmacokinetic (PK) profiles of WILATE were determined by FVIII activity, VWF:RCo, VWF:Ag, and VWF:CB obtained from an open label, prospective, randomized, controlled, two-arm cross-over study with WILATE and a comparator product conducted at 6 sites in the US. Twenty-two subjects with inherited VWD [type 1, n=6; type 2, n=9 (6 type 2A, 1 type 2B, and 2 type 2M); and type 3, n=7] received an intravenous bolus dose of WILATE containing approximately 40 IU of VWF:RCo/kg body weight. Twenty subjects completed the study as per protocol. PK parameters for VWF:RCo and FVIII activities are summarized in Table 4 and Table 5, respectively.
The PK parameters reported in Table 4 are based on VWF:RCo values obtained using a modified Behring Coagulation System (BCS) analytical method. The modified BCS was used because of its validated lower variability compared with the standard BCS. Measured concentrations (IU VWF:RCo/mL) are higher by the modified BCS than by the standard BCS analytical method which is used in some clinical laboratories. Dose adjusted Cmax and AUC determined by this modified BCS method are approximately 1.5 times higher than those by the standard BCS method. No difference has been found in incremental recovery.
Table 4 : Pharmacokinetic Parameters of VWF:RCo:mean ±
SD (range)
| Parameters | VWD type I (n = 5) |
VWD type II (n = 9) |
VWD type III (n = 6) |
Total (n = 20) |
| Cmax (IU/dL) |
74 ± 13 (62 - 91) |
77 ± 18 (40 - 100) |
79 ± 13 (65 - 102) |
76 ± 15 (40 - 102) |
| AUC (0-inf) (IU*hr/dL) |
1633 ± 979 (984 - 3363) |
1172±421 (571 - 1897) |
995 ± 292 (527 - 1306) |
1235 ±637 (527 - 3363) |
| Half-life (hrs) |
24.7 ± 17.9 (11.2 - 48.5 ) |
15.3 ± 6.3 (6.0 - 26.4) |
9.1± 2.6 (5.7 - 12.9 ) |
15.8 ± 11.0 (5.7 - 48.5) |
| CL (mL/h/kg) |
3.1 ± 1.1 (1.2 - 4.1) |
4.1 ± 1.7 (2.0 - 7.1) |
4.2 ± 1.4 (3.0 - 6.6) |
3.9 ± 1.5 (1.2 - 7.1) |
| Vss (mL/kg) |
81.7 ± 38.5 (15.3 - 74.2) |
76.6 ± 35.4 (45.3 - 158.8) |
49.4 ± 16.7 (29.7 - 67.1) |
69.7 ± 33.2 (29.7 - 158.8) |
| MRT (hrs) |
32.7 ± 25.8 (15.3 - 74.2) |
19.7 ± 5.6 (9.9 - 27.1) |
11.9 ± 2.9 (9.2 - 15.9) |
20.6 ± 14.8 (9.2 - 74.2) |
| Recovery (%IU/kg) |
1.8 ± 0.2 (1.5 - 2.0) |
1.8 ± 0.5 (1.0 - 2.4) |
2.1 ± 0.3 (1.8 - 2.6) |
1.9 ± 0.4 (1.0 - 2.6) |
| Cmax = peak concentration; AUC = area under curve; CL = clearance; Vss = volume of distribution at steady state; MRT = mean residence time | ||||
Table 5 : Pharmacokinetic Parameters of FVIII
activity: mean ± SD (range) – chromogenic
| Parameters | VWD type I (n = 5) |
VWD type II (n = 8*) |
VWD type III (n = 6) |
Total (n = 19*) |
| Cmax (IU/dL) |
117.1 ± 12.1 (103 - 135) |
147.2 ± 32.6 (102 - 206) |
120 ± 23 (91 - 148) |
112 ± 23 (59 - 148) |
| AUC (0-inf) (IU*hr/dL) |
1187±382 (523 - 1483) |
1778 ± 1430 (544 - 4821) |
2670 ± 854 (1874 - 3655) |
2290 ±1045 (464 - 4424) |
| Half-life (hrs) |
17.5 ± 4.9 (10.9 - 23.8) |
23.6 ± 8.3 (12.6 - 34.7) |
16.1 ± 3.1 (11.8 - 20.1) |
19.6 ± 6.9 (10.9 - 34.7) |
| CL (mL/h/kg) |
4.4 ± 3.7 (2.5 - 11.0) |
2.5 ± 0.9 (1.2 - 3.5) |
2.0 ± 0.6 (1.4 - 2.8) |
2.9 ± 2.1 (1.2 - 11.0) |
| Vss (mL/kg) |
95.0 ± 53.8 (57.1 - 190.0) |
79.5 ± 23.1 (52.8 - 116.2) |
44.2 ± 10.4 (31.8 - 57.1) |
72.4 ± 36.2 (31.8 - 190.0) |
| MRT (hrs) |
24.1 ± 5.5 (17.2 - 31.5) |
35.1 ± 14.2 (17.5 - 61.6) |
23.0 ± 3.7 (18.0 - 27.7) |
28.4 ± 11.1 (17.2 - 61.6) |
| Recovery (%IU/kg) |
1.9 ± 0.5 (1.1 - 2.5) |
2.2 ± 0.4 (1.6 - 2.8) |
2.5 ± 0.5 (2.0 - 3.0) |
2.2 ± 0.5 (1.1 - 3.0) |
| *One subject with implausible long half-life is not included in the summary table, except for recovery result. Cmax = peak concentration; AUC = area under curve; CL = clearance; Vss = volume of distribution at steady state; MRT = mean residence time |
Clinical efficacy of WILATE in the control of bleeding in subjects with VWD was determined in four prospective, open-label, non-controlled clinical studies (excluding PK study). For inclusion in the studies, subjects had to have inherited VWD (any type) that did not respond to desmopressin acetate. Subjects aged ≥ 12 to ≤ 65 years were eligible to enter three of the four studies, and subjects aged ≥ 6 to ≤ 85 years were eligible for one study. Exclusion criteria included the administration of other plasma-derived or blood products or desmopressin acetate 15 days before study entry, administration of acetylsalicylic acid 7 days before study entry, symptomatic infection, past or present inhibitor activity (3 studies), and severe liver or kidney disease (3 studies). A total of 70 VWD subjects with a mean age of 37 years (range 5–77 years) were enrolled in the studies, of whom 37 were type 3 and 30 were male. The total number of exposure days to WILATE for all investigations across the four studies ranged from 202 to 4917 days. Treated BEs were analyzed for efficacy using a set of objective criteria in addition to a subjective 4-point hemostatic efficacy scale (excellent, good, moderate and none) which was determined at the discretion of the investigator. In assessing efficacy using the objective criteria, treatment of a bleeding episode was classified as a success when none of the criteria listed below were met:
BEs treated with WILATE are summarized for all subjects (n=45) and subjects aged 5–16 years (n=11) in Table 6. Among the 70 VWD subjects administered WILATE in clinical studies (excluding the PK study), 45 received on demand treatment for 1068 BEs. Using the above objective criteria, corresponding efficacy for each bleeding event was rated as being successful in 84% of the episodes. In these 45 subjects with BEs, 93% of the successfully treated BEs occurred in VWD type 3 subjects (n=25). In 11 pediatric patients aged 5–16 years, efficacy was rated as being successful in 87.6% of BEs.
Table 6 :Proportion of Successful Treatments of
Bleeding Episodes with WILATE
| Number of BEs* | Number of successfully treated BEs | % Successes (95% CI) | |
| All subjects (n=45) | 1068 | 898 | 84.1 (81.8-86.2 |
| Subjects 5-16 years (n=11) | 234 | 205 | 87.6 (82.7-91.5) |
| *A “bleeding episode” may involve bleeding at multiple sites in this analysis. | |||
Dosing information for 972 successfully treated “bleeding episodes” (1423 infusions), and 211 successfully treated bleeding episodes (289 infusions) in subjects aged 5–16 years, for regional bleeding is summarized in Table 7. For the purpose of assigning success/failure to regional bleeding that occurred at the same time, bleeding at different sites over the same time span was counted as separate BEs. Thus, the number of these “episodes” is different from that in the overall evaluation for success/failure of WILATE in the treatment of BEs in Table 6. The majority of BEs were treated for 1-3 days. In subjects with GI bleeds, the duration for product use to control bleeding was longer (up to 7 days).
Table 7 : Administered Dosages (VWF:RCo in IU/kg) in
Bleeding Episodes* Successfully Treated with WILATE: Mean ± SD (Range)
| Location | All Subjects
(n=45) |
Subjects 5-16 years
(n=11) |
||||||
| Initial Dose | Subsequent Doses | Initial Dose | Subsequent Doses | |||||
| # of Infusions | Dose: Mean ± SD (Range) | # of Infusions | Dose: Mean ± SD (Range) | # of Infusions | Dose: Mean ± SD (Range) | # of Infusions | Dose: Mean ± SD (Range) | |
| Joints | 542 | 28 ± 13 (7 - 69) |
259 | 21 ± 10 (7 - 60) |
117 | 32 ± 13 (14 - 69) |
41 | 25 ± 9 (12 - 62) |
| Epistaxis | 91 | 25 ± 10 (13 - 78) |
41 | 22 ± 14 (8 - 77) |
25 | 25 ± 10 (14 - 52) |
5 | 37 ± 25 (12 - 77) |
| GI Tract | 64 | 43 ± 19 (9 - 76) |
61 | 36 ± 21 (9 - 76) |
1 | 22 (N/A) |
0 | N/A |
| Oral | 33 | 27 ± 14 (10 - 80) |
8 | 24 ± 18 (8 - 60) |
21 | 24 ± 8 (16 - 52) |
2 | 25 ± 13 (16 - 35) |
| Gynecologic | 52 | 28 ± 17 (12 - 77) |
35 | 26 ± 9 (9 - 52) |
33 | 27 ± 16 (12 - 69) |
25 | 26 ± 8 (12 - 52) |
| Other** | 189 | 24 ± 12 (12 - 95) |
48 | 20 ± 13 (10 - 95) |
14 | 27 ± 7 (19 - 37) |
5 | 19 ± 4 (16 - 26) |
| *For the purpose of this analysis, bleeding at each site
is counted as a separate “episode”. **“Other” includes mostly muscle bleeds, hematuria, ecchymosis, hematoma and other miscellaneous sites of bleeding. |
||||||||
A prospective, open-label, single-arm, uncontrolled, multi-center clinical study was conducted to investigate the safety and hemostatic efficacy of WILATE in 28 subjects (19 female and 9 male) who underwent 30 surgeries. Two female subjects underwent 2 surgeries each. Subjects ranged in age from 12 to 74 years (median = 36). Three subjects were between 12 and 17 years old and 4 were 65 years or older. Six subjects had type 1 VWD, 1 had type 2A, 1 type 2B, and 20 had type 3 VWD. One type 1 and one type 3 subject had 2 surgeries each.
Twenty-one surgeries were classified as major (e.g. orthopedic joint replacement, cesarean section and vaginal deliveries, laminectomy, tonsillectomy, appendectomy, 3rd molar extractions) and 9 were classified as minor (e.g. menisectomy, teeth extractions other than 3rd molars, septoplasty, biopsy). Seven surgeries (3 major, 4 minor) were performed in type 1 VWD subjects, 2 surgeries (1 major, 1 minor) were performed in type 2 (A/B) VWD subjects, and 21 surgeries (17 major, 4 minor) were performed in type 3 VWD subjects. The types of surgery for the 9 minor procedures were: dental (n=5, 55.6%); orthopedic (n=2, 22.2%); ophthalmologic (n=1, 11.1%); and ear, nose and throat (n=1, 11.1%). The types of surgery for the 21 major procedures were: orthopedic (n=8, 38.1%); obstetric/gynecological (n=5, 23.8%); gastrointestinal (n=4, 19.0%); dental (n=2, 9.5%); and ear, nose and throat (n=2, 9.5%). The type of surgery according to VWD type were: VWD type 1 (n=7) – dental (n=4, 57.1%), orthopedic (n=2, 28.6%), and ear, nose and throat (n=1, 14.3%); VWD type 2 (A/B) (n=2) – orthopedic (n=1, 50%), and obstetric/gynecological (n=1, 50%); VWD type 3 (n=21) – orthopedic (n=7, 33.3%), gastrointestinal (n=4, 19.0%), obstetric/gynecological (n=4, 19.0%), dental (n=3, 14.3%), ear, nose and throat (n=2, 9.5%), and ophthalmologic (n=1, 4.8%).
Dosing was individualized based on in-vivo recovery results performed before surgery. Mean total loading dose per infusion was 51.4 IU/kg (median 52.1 IU/kg; range 27-77 IU/kg). Major surgeries required a mean loading dose of 54.7 IU/kg (median 55.5 IU/kg; range 36-69 IU/kg) in comparison with a mean loading dose of 41.9 IU/kg (median 37.5 IU/kg; range 27-77 IU/kg) for minor surgeries. Mean total maintenance dose per infusion was 28.5 IU/kg (median 28.5 IU/kg; range 8-63 IU/kg). Major surgeries required a mean maintenance infusion of 29.6 IU/kg (median 30 IU/kg; range 8-63 IU/kg) in comparison with a mean maintenance infusion of 21.6 IU/kg (median 20.6 IU/kg; range 14-38 IU/kg) for minor surgeries.
Efficacy of WILATE in surgical procedures was assessed by the surgeon at the conclusion of surgery and by the investigator-hematologist at 24 hours following completion of the final maintenance dose. Efficacy of WILATE was assessed using a stringent and objective 4-point ordinal efficacy scale (excellent, good, moderate, or none) based on estimated expected versus actual blood loss, transfusion requirements and post-operative bleeding and oozing. A rating of excellent or good was required to declare the outcome a success. An independent data monitoring committee (IDMC) additionally conducted an independent post hoc adjudication of intra- and post-operative assessments made by the surgeon/investigator-hematologist. In situations where the IDMC's assessment differed from that of the surgeon and/or investigator-hematologist, the IDMC assessment took priority.
The overall efficacy of WILATE treatment for surgical procedures in this study was 96.7%. Treatment with WILATE was successful in all minor surgeries and in 95.2% of major surgeries (Table 13). It was also successful in all surgical procedures in VWD type 3 and type 2 subjects and in 85.7% of procedures in VWD type 1 subjects (Table 14). One failure was reported in a VWD type 1 subject undergoing lumbar laminectomy (major surgery) who experienced slightly greater blood loss (25 mL) than the expected maximum (20 mL).
Table 13 : Hemostatic Efficacy Assessment by Severity
of Surgery as Adjudicated by the IDMC (n=30)
| Efficacy grade | Minor (n=9) |
Major (n=21) |
All surgeries (n=30) |
||||||
| n (%) | Rate | 98.75% CI | n (%) | Rate | 98.75% CI | n (%) | Rate | 98.75% CI | |
| Success | 9 (100) | 1.000 | 0.569, 1.000 | 20 (95.2) | 0.952 | 0.704, 1.000 | 29 (96.7) | 0.967 | 0.784, 1.000 |
| Failure | 0 | 1 (4.8) | 1 (3.3) | ||||||
| CI = confidence interval; IDMC = Independent Data Monitoring Committee; n = number of surgeries; rate = overall success rate. | |||||||||
Table 14 : Hemostatic Efficacy Assessment by Type of
VWD as Adjudicated by the IDMC (n=30)
| Efficacy grade | VWD type 1 | VWD type 2 | VWD type 3 | ||||||
| n (%) | Rate | 98.75% CI | n (%) | Rate | 98.75% CI | n (%) | Rate | 98.75% CI | |
| Overall IDMC assessment Success | 6 (85.7) | 0.857 | 0.328, 0.999 | 2 100) | 1.000 | 0.079, 1.000 | 21 (100) | 1.000 | 0.785, 1.000 |
| Failure | 1 (14.3) | 0 | 0 | ||||||
| CI = confidence interval; IDMC = Independent Data Monitoring Committee; n = number of surgeries; rate = overall success rate; VWD = von Willebrand Disease. | |||||||||
In this study, actual blood loss (median) was lower than the expected maximal estimated blood loss in all types of surgeries. The actual blood loss was also lower than the average predicted blood loss in minor surgeries and equal in major surgeries (Table 15).
Table 15 : Expected and Actual Estimated Blood Loss
during Surgery
| Estimated Blood Loss | Minor Surgery (n = 9) |
Major Surgery (n= 21) |
| Expected Maximum - Median (range) mL | 50 (1-200) | 500 (20-2000) |
| Expected Average - Median (range) mL | 20 (1-100) | 100 (5-1500) |
| Actual - Median (range) mL | 15 (1-50) | 100 (0-1200) |
Intra-operative transfusion was predicted in 5 subjects, but actually given in only 2. One subject received platelets intra-operatively for previously existing thrombocytopenia and one subject who underwent abdominal hysterectomy received one infusion of rejuvenated (in biochemical solution) packed red blood cells intra-operatively which was planned pre-surgery.
Three subjects received transfusions following surgery due to anemia and low hemoglobin values seen post-operatively.
REFERENCES
9. Mannucci P.M.: Treatment of von Willebrand's disease. New England Journal of Medicine 2004;351:683-694
WILATE von Willebrand
Factor/Coagulation Factor VIII Complex
(Human)
Please read this Patient Information carefully before using WILATE and each time you get a refill, as there may be new information. This Patient Information does not take the place of talking with your healthcare provider about your medical condition or your treatment.
What is WILATE?
WILATE is an injectable medicine that is used to treat bleeding in adults and children with severe von Willebrand disease (VWD) as well as patients with mild or moderate VWD in whom the use of desmopressin is known or suspected to be ineffective or contraindicated.
WILATE is also used for the prevention of excessive bleeding during and after surgery in adults and children with VWD.
Who should not use WILATE?
You should not use WILATE if you are allergic to von Willebrand Factor or Factor VIII or any of the other ingredients of WILATE.
What should I tell my healthcare provider before using WILATE?
Talk to your healthcare provider about any medical conditions that you have or have had.
Tell your healthcare provider about all of the prescription and non-prescription medicines you take, including over-the-counter medicines, dietary supplements, or herbal medicines.
Tell your healthcare provider if you are pregnant or nursing because WILATE might not be right for you.
How should I use WILATE?
You get WILATE as an infusion into your vein after reconstitution of the lyophilized powder by mixing it with the supplied 5 or 10 milliliter sterile solvent (Water for Injection with 0.1% Polysorbate) with the supplied transfer device (see instruction for reconstitution and injection of WILATE).
Your healthcare provider will instruct you on how to do reconstitutions and infusions using sterile technique on your own or with the help of a family member, and they may watch you give yourself the first dose of WILATE.
You must carefully follow your healthcare provider's instructions regarding the dose and schedule for infusing WILATE so that your treatment will work the best that it can for you.
WILATE comes in different dosage strengths. The actual number of international units (IU) of von Willebrand Factor and Factor VIII in the vial will be imprinted on the label and box. Always check the actual dosage strength printed on the label to make sure you are using the strength prescribed by your healthcare provider.
Contact your healthcare provider right away if bleeding is not controlled after using WILATE.
Talk to your healthcare provider before travelling. Plan to bring enough WILATE for your treatment during this time.
If you forget to use WILATE, do not inject a double dose to make up for the forgotten dose. Proceed with the next infusion as scheduled.
Do not stop using WILATE without consulting with your healthcare provider.
What are the possible side-effects of WILATE?
Allergic reactions may occur. Call your healthcare provider or emergency department right away if you have any of the following symptoms: difficulty breathing, chest tightness, swelling of the face, rash or hives.
Because it is made from human blood, there is the risk that WILATE can potentially transmit disease or cause allergic reactions. Tell your healthcare provider if you have low-grade fever, rash, joint pain, nausea, vomiting, feeling tired, and yellowing of the skin.
Common side effects of WILATE are hypersensitivity reactions including urticaria (rash) dizziness, and testing positive for a common virus (parvovirus B19).
These are not all of the possible side effects from WILATE. Ask your healthcare provider for more information. You are encouraged to report side effects to Octapharma USA Inc. at 1-866-766-4860 or FDA at 1-800-FDA-1088.
Talk to your healthcare provider about any side-effect that bothers you or that does not go away.
How should I store WILATE?
Keep WILATE in its original box to protect it from exposure to light. Do not freeze WILATE .
You can store WILATE for up to 36 months at +2°C to +8°C (36°F to 46°F) from date of manufacture. Within this period, WILATE may be stored for a period of up to 6 months at room temperature (maximum of +25°C or 77°F). Note on the carton the date which the product was removed from the refrigerator.
After storage at room temperature, the product must be used or discarded, and it must not be put back into the refrigerator.
Do not use WILATE after the expiration date printed on the vial.
Do not use WILATE if the reconstituted solution is cloudy, contains particles, or is not colorless.
Use WILATE immediately after mixing.
Dispose all materials, including any unused WILATE , in an appropriate container.
What else should I know about WILATE?
Do not use WILATE for a medical condition for which it was not prescribed. Do not share WILATE with other people, even if they have the same diagnosis and symptoms that you have.
Recredits at Octapharma available to patients
For more product information on WILATE, please visit www.wilateusa.com
For more information on patient assistance programs that are available to you, please contact the Octapharma Patient Support Center at 1-800-554-4440.
Manufactured by : Octapharma Pharmazeutika Produktionsges.m.b.H., Oberlaaer Strasse 235, A-1100 Vienna, Austria, U.S. License No. 1646. Distributed by : Octapharma USA, Inc., 121 River Street, 12th floor, Hoboken, NJ 07030
Instructions for Use
WILATE von Willebrand
Factor/Coagulation Factor VIII Complex
(Human)
WILATE is supplied as a powder. Before it can be infused in your vein (intravenous injection), you must mix the powder with the supplied liquid diluent.
Do not attempt to do an infusion to yourself unless you have been taught how by your healthcare provider or hemophilia center.
Always follow the specific instructions given by your healthcare provider. The steps listed below are general guidelines for using WILATE. If you are unsure of the procedures, please call you healthcare provider before using WILATE. Your healthcare provider will prescribe the dose that you should take.
Preparation and Reconstitution
1) Warm the WILATE and diluent vials in the closed vials up to room temperature. If a water bath is used for warming, avoid water contact with the rubber stoppers or the caps of the vials. The temperature of the water bath should not exceed +37°C (98°F).
2) Remove the caps from the WILATE vial and the diluent vial and clean the rubber stoppers with an alcohol swab.
3) Peel away the lid of the outer package of the Mix2Vial™ transfer set. To maintain sterility, leave the Mix2Vial™ device in the clear outer packaging. Place the diluent vial on a level surface and hold the vial firmly. Take the Mix2Vial™ in its outer package and invert it over the diluent vial. Push the blue plastic cannula of the Mix2Vial™ firmly through the rubber stopper of the diluent vial (Fig. 1). While holding onto the diluent vial, remove the outer package from the Mix2Vial™, leaving the Mix2Vial™ attached firmly to the diluent vial (Fig. 2).
Figure 1 and 2
 |
4) With the WILATE vial held firmly on a level surface, quickly invert the diluent vial with the Mix2Vial™ attached and push the transparent plastic cannula end of the Mix2Vial™ firmly through the stopper of the WILATE vial (Fig. 3). The diluent will be drawn into the WILATE vial by the vacuum.
Figure 3
 |
5) With both vials still attached, gently swirl the WILATE vial to ensure the powder is fully dissolved to a clear solution. Do not shake the vial in order to avoid foaming. Once the contents of the WILATE vial are completely dissolved, firmly hold both the transparent and blue parts of the Mix2Vial™. Unscrew the Mix2Vial™ into two separate pieces (Fig. 4) and discard the empty diluent vial and the blue part of the Mix2Vial™.
The final solution is clear or slightly opalescent, colorless or slightly yellow. If the concentrate fails to dissolve completely or an aggregate is formed, do not use the preparation.
Figure 4
 |
Administration
For intravenous use after reconstitution only.
