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CEPROTIN
[Protein C Concentrate (Human)] for Injection
CEPROTIN [Protein C Concentrate (Human)] is manufactured from human plasma purified by a combination of filtration and chromatographic procedures, including a column of immobilized mouse monoclonal antibodies on gel beads. see WARNINGS AND PRECAUTIONS: Transmission Of Infectious Agents.
The manufacturing process for CEPROTIN includes processing steps designed to reduce the risk of viral transmission. The capacity of the manufacturing process to remove and/or inactivate enveloped and non-enveloped viruses has been validated by laboratory spiking studies on a scaled down process model, using the following enveloped and non-enveloped viruses: Human Immunodeficiency Virus Type 1 (HIV-1), Bovine Viral Diarrhea Virus (BVDV ), Tick-Borne Encephalitis Virus (TBEV), Pseudorabies Virus (PRV), Hepatitis A Virus (HAV) and Mice Minute Virus (MMV). Virus reduction steps consist of detergent treatment (Polysorbate 80, P80), heat inactivation (Vapor Heating) and immunoaffinity chromatography (IAX).
Virus clearance studies for CEPROTIN have demonstrated that the process provides for a robust overall virus clearance capacity. A summary of log virus reduction factors per virus and manufacturing step is presented in Table 2.
Table 2 Summary of Mean Log10 Virus Reduction Factors for the
CEPROTIN Manufacturing Process
| Manufact-uring Step |
HIV-1 | HCV Model Viruses |
PRV | HAV | MMV | |
| BVDV | TBEV | |||||
| P80 Treatment | >5.1 | >4.7 | n.d. | 2.5* | >3.8* | 1.4* |
| IAX | 5.7 | n.d. | 4.8 | 5.4 | 3.1 | 3.6 |
| Vapor Heating | 4.6 | >5.9 | n.d. | 5.9 | >4.2 | 1.2 |
|
Abbreviations: IEX, Ion Exchange Chromatography; IAX, Immunoaffinity
Chromatography; HIV-1, Human Immunodeficiency Virus Type I; TBEV,
Tick-Borne Encephalitis Virus (model for hepatitis C virus); BVDV, Bovine
Viral Diarrhea Virus (model virus for HCV and other small, enveloped RNA
viruses); PRV, Pseudorabies Virus (model virus for enveloped DNA
viruses, e.g. HBV, Hepatitis B Virus); HAV, Hepatitis A Virus; MMV, Mice
Minute Virus (model for Human Parvovirus B19 and for non enveloped
viruses); n.d., not done. * Coupled with IEX. I |
||||||
CEPROTIN is indicated for pediatric and adult patients with severe congenital Protein C deficiency for the prevention and treatment of venous thrombosis and purpura fulminans.
For intravenous administration only.
Initiate treatment with CEPROTIN under the supervision of a physician experienced in replacement therapy with coagulation factors /inhibitors where monitoring of protein C activity is feasible.
The dose, administration frequency and duration of treatment with CEPROTIN depends on the severity of the protein C deficiency, the patient's age, the clinical condition of the patient and the patient's plasma level of protein C. Therefore, adjust the dose regimen according to the pharmacokinetic profile for each individual patient. see Protein C Activity Monitoring.
Table 1 provides the CEPROTIN dosing schedule for acute episodes, short-term prophylaxis and longterm prophylaxis.
Table 1 CEPROTIN Dosing Schedule for Acute Episodes, Short-term
Prophylaxis and Long-term Prophylaxis*
| Initial Dose† | Subsequent 3 Doses† |
Maintenance Dose† |
|
| Acute Episode /
Short-term Prophylaxis‡ |
100-120 IU/kg | 60 - 80 IU/kg Q 6 hours |
45 - 60 IU/kg Q 6 or 12 hours |
| Long-term Prophylaxis |
NA | NA | 45 - 60 IU/kg Q 12 hours |
| NA = Not applicable; Q = every. * Dosing is based upon a pivotal clinical trial of 15 patients. † The dose regimen should be adjusted according to the pharmacokinetic profile for each individual. (General, Protein C Activity Monitoring) ‡CEPROTIN should be continued until desired anticoagulation is achieved. |
|||
An initial dose of 100-120 IU/kg for determination of recovery and half-life is recommended for acute episodes and short-term prophylaxis. Subsequently, adjust the dose to maintain a target peak protein C activity of 100 %. After resolution of the acute episode, continue the patient on the same dose to maintain trough protein C activity level above 25% for the duration of treatment.
In patients receiving prophylactic administration of CEPROTIN, higher peak protein C activity levels may be warranted in situations of an increased risk of thrombosis (such as infection, trauma, or surgical intervention). Maintenance of trough protein C activity levels above 25% is recommended.
These dosing guidelines are also recommended for neonatal and pediatric patients. see Use In Specific Populations: Pediatric Use and CLINICAL PHARMACOLOGY: Pharmacokinetics.
The measurement of protein C activity using a chromogenic assay is recommended for the determination of the patient's plasma level of protein C before and during treatment with CEPROTIN. The half-life of CEPROTIN may be shortened in certain clinical conditions such as acute thrombosis, purpura fulminans and skin necrosis. see CLINICAL PHARMACOLOGY: Pharmacokinetics. In the case of an acute thrombotic event, it is recommended that protein C activity measurements be performed immediately before the next injection until the patient is stabilized. After the patient is stabilized, continue monitoring the protein C levels to maintain the trough protein C level above 25%.
Patients treated during the acute phase of their disease may display much lower increases in protein C activity. Coagulation parameters should also be checked; however, in clinical trials data were insufficient to establish correlation between protein C activity levels and coagulation parameters.
In patients starting treatment with oral anticoagulants belonging to the class of vitamin K antagonists, a transient hypercoagulable state may arise before the desired anticoagulant effect becomes apparent.
This transient effect may be explained by the fact that protein C, itself a vitamin K-dependent plasma protein, has a shorter half-life than most of the vitamin K-dependent proteins (i.e. Factor II, IX and X).
In the initial phase of treatment, the activity of protein C is more rapidly suppressed than that of the procoagulant factors. For this reason, if the patient is switched to oral anticoagulants, protein C replacement must be continued until stable anticoagulation is obtained. Although warfarin-induced skin necrosis can occur in any patient during the initiation of treatment with oral anticoagulant therapy, individuals with severe congenital protein C deficiency are particularly at risk.
During the initiation of oral anticoagulant therapy, it is advisable to start with a low dose of the anticoagulant and adjust this incrementally, rather than use a standard loading dose of the anticoagulant.
Use Aseptic Technique
Use Aseptic Technique
Visually inspect CEPROTIN for particulate matter and discoloration prior to administration.
After reconstitution, the solution should be colorless to slightly yellowish and clear to slightly opalescent and free of visible particles. Do not use the solution if it does not meet this criteria. Administer CEPROTIN at room temperature not more than 3 hours after reconstitution.
Record the name and batch number of the product every time CEPROTIN is administered to a patient.
Administer CEPROTIN at a maximum injection rate of 2 mL per minute except for children with a body weight of < 10 kg, where the injection rate should not exceed a rate of 0.2 mL/kg/minute.
CEPROTIN is available in single-dose vials that contain nominally 500 (blue color bar) or 1000 (green color bar) International Units (IU) human protein C and is reconstituted with 5 mL and 10 mL of Sterile Water for Injection, respectively to provide a single dose of human Protein C at a concentration of 100 IU/mL.
CEPROTIN, when reconstituted with the appropriate volume of diluent, contains the following excipients: 8 mg/mL human albumin, 4.4 mg/mL trisodium citrate dihydrate and 8.8 mg/mL sodium chloride.
CEPROTIN is supplied as a sterile, white or cream colored, lyophilized powder for IV injection. It has a pH between 6.7 and 7.3 and an osmolality not lower than 240 mosmol/kg. One International Unit (IU) of protein C corresponds to the amidolytically measured activity of protein C in 1 mL of normal plasma.
The potency (IU) is determined using a chromogenic substrate method referenced against the World
Health Organization (WHO) International Standard (86/622).
CEPROTIN is available in single-dose vials that contain the following nominal product strengths:
 |
- 500 IU per vial: (NDC: 0944-4177-05)
 |
- 1000 IU per vial: (NDC: 0944-4179-10)
Actual potency is printed on the vial label.
One package of CEPROTIN contains one glass vial of CEPROTIN powder, one glass vial of Sterile Water for Injection, USP, one transfer needle, one filter needle, one full prescribing physician insert and one patient package insert.
CEPROTIN, packaged for sale, is stable for 3 years when stored refrigerated at 2°C–8°C (36°F-46°F). Do not freeze in order to prevent damage to the diluent vial. Store the vial in the original carton to protect it from light. The reconstituted solution should be used within 3 hours of reconstitution. Do not use beyond the expiration date on the CEPROTIN vial.
Manufacture by: Baxalta US Inc. Lexington, MA 02421 USA. Revised: Sep 2018
The common adverse reactions related to CEPROTIN treatment observed were the following hypersensitivity or allergic reactions: lightheadedness and itching and rash.
Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in one clinical study of a drug cannot be directly compared with rates in the clinical studies of the same drug or another drug and may not reflect the rates observed in practice.
The safety profile of CEPROTIN was based on 121 patients from clinical studies and compassionate use in severe congenital Protein C deficiency. Duration of exposure ranged from 1 day to 8 years. One patient experienced hypersensitivity/allergic reactions (itching and rash) and lightheadedness which were determined by the investigator to be related to CEPROTIN.
No inhibiting antibodies to CEPROTIN have been observed in clinical studies. However, the potential for developing antibodies cannot be ruled out.
The following adverse reactions have been identified during postapproval use of CEPROTIN:
Psychiatric Disorders: Restlessness
Skin and Subcutaneous Tissue Disorders: Hyperhydrosis
General Disorders and Administration Site Conditions: Injection Site Reaction
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 drug exposure.
No formal drug interaction studies have been conducted.
see WARNINGS AND PRECAUTIONS: Bleeding Episodes for information regarding simultaneous administration of CEPROTIN and tissue plasminogen activator (tPA).
see DOSAGE AND ADMINISTRATION: Initiation Of Vitamin K Antagonists for information regarding use of CEPROTIN and vitamin K antagonists.
Included as part of the "PRECAUTIONS" Section
CEPROTIN may contain traces of mouse protein and/or heparin as a result of the manufacturing process. Allergic reactions to mouse protein and/or heparin cannot be ruled out. If symptoms of hypersensitivity/allergic reaction occur, discontinue the injection/infusion. In case of anaphylactic shock, the current medical standards for treatment are to be observed.
Because CEPROTIN is made from human plasma, it may carry a risk of transmitting infectious agents, e.g., viruses, and theoretically, the Creutzfeldt-Jakob disease (CJD) agent.
ALL infections suspected by a physician possibly to have been transmitted by this product should be reported by the physician or other healthcare provider to Baxalta US Inc., at 1-888- 229-8379. Discuss the risks and benefits of this product with your patient.
Several bleeding episodes have been observed in clinical studies. Concurrent anticoagulant medication may have been responsible for these bleeding episodes. However, it cannot be completely ruled out that the administration of CEPROTIN further contributed to these bleeding events.
Simultaneous administration of CEPROTIN and tissue plasminogen activator (tPA) may further increase the risk of bleeding from tPA.
CEPROTIN contains trace amounts of heparin which may lead to Heparin-induced Thrombocytopenia, which can be associated with a rapid decrease of the number of thrombocytes. Identifying HIT is complicated because these symptoms may already be present in acute phase patients with severe congenital protein C deficiency. Determine the platelet count immediately and consider discontinuation of CEPROTIN.
Inform patients on a low sodium diet that the quantity of sodium in the maximum daily dose of CEPROTIN exceeds 200 mg. Monitor patients with renal impairment closely for sodium overload.
Inform patients of the early signs of hypersensitivity reactions including hives, generalized urticaria, tightness of the chest, wheezing, hypotension and anaphylaxis, as the risk of an allergic type hypersensitivity reaction cannot be excluded. In addition, CEPROTIN may contain traces of mouse protein or heparin as a result of the manufacturing process. Allergic reactions to mouse protein or heparin cannot be ruled out. Inform patients to immediately discontinue the injection/infusion and inform their physician as soon as possible if symptoms of hypersensitivity/allergic reaction occur. Maintain CEPROTIN in the original carton to protect from light prior to reconstitution.
Reconstitute the lyophilized CEPROTIN powder with the supplied diluent (Sterile Water for Injection) using the sterile transfer needle. Gently swirl the vial until all powder is dissolved.
Visually inspect the solution for discoloration and particulate matter. The reconstituted solution should be colorless to slightly yellowish and clear to slightly opalescent and free from visible particles. Do not administer CEPROTIN if discoloration or particulate matter is observed. The solution is drawn through the sterile filter needle into a sterile disposable syringe.
The reconstituted solution contains no preservatives and is intended for single use only. Once reconstituted, administer the product by intravenous injection within 3 hours. Appropriately discard all unused solution, empty vials and used needles.
The attached CEPROTIN (Protein C Concentrate [Human]) "Information For Patients" contains more detailed instructions on the preparation of CEPROTIN.
Protein C contained in CEPROTIN is a normal constituent of human plasma and acts like endogenous protein C. Studies in heterologous species to evaluate carcinogenicity, reproductive toxicology and developmental toxicology have not been performed.
CEPROTIN has not demonstrated mutagenic potential in the Salmonella Thyphimurium reverse mutation assay (Ames test).
Animal reproduction studies have not been conducted with CEPROTIN. It is also not known whether CEPROTIN can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. CEPROTIN should be given to pregnant women only if clearly needed.
CEPROTIN has not been studied for use during labor and delivery. Use only if clearly needed.
CEPROTIN has not been studied for use in nursing mothers. Use CEPROTIN only if clearly needed.
Neonatal and pediatric subjects were enrolled during the prospective and retrospective studies described in CLINICAL STUDIES (14). Of the 18 subjects enrolled during the prospective study, 1 was newborn, 3 were between 28 days and 23 months, 9 were between 2 and 11 years, 1 was between 12 and 16 years, and 4 were older than 16 years [see Clinical Studies: Pivotal Study]. Of the 11 subjects enrolled and treated during the retrospective study, 9 were between 2 and 11 years, and 2 were older than 16 years [see Clinical Studies: Retrospective Analysis].
Clinical studies of CEPROTIN did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects.
No experience in the treatment of patients with renal and/or hepatic impairment is available.
No Information Provided
None known.
Protein C is the precursor of a vitamin K-dependent anticoagulant glycoprotein (serine protease) that is synthesized in the liver. see DOSAGE AND ADMINISTRATION: Initiation Of Vitamin K Antagonists. It is converted by the thrombin/thrombomodulin-complex on the endothelial cell surface to activated Protein C (APC). APC is a serine protease with potent anticoagulant effects, especially in the presence of its cofactor protein S. APC exerts its effect by the inactivation of the activated forms of factors V and VIII, which leads to a decrease in thrombin formation. APC has also been shown to have profibrinolytic effects.
The Protein C pathway provides a natural mechanism for control of the coagulation system and prevention of excessive procoagulant responses to activating stimuli. A complete absence of protein C is not compatible with life. A severe deficiency of this anticoagulant protein causes a defect in the control mechanism and leads to unchecked coagulation activation, resulting in thrombin generation and intravascular clot formation with thrombosis.
In clinical studies, the intravenous administration of CEPROTIN demonstrated a temporary increase, within approximately half an hour of administration, in plasma levels of APC. Replacement of protein C in protein C-deficient patients is expected to control or, if given prophylactically, to prevent thrombotic complications.
Table 3 provides pharmacokinetic results for asymptomatic and symptomatic subjects with protein C deficiency.
Table 3: Pharmacokinetics of CEPROTIN in Subjects with Severe
Congenital Protein C Deficiency
| PK parameter | N | Median | 95% CI for median | Min | Max |
| Cmax[IU/dL] | 21 | 110 | 106 to 127 | 40 | 141 |
| Tmax[h] | 21 | 0.50 | 0.50 to 1.05 | 0.17 | 1.33 |
| Incremental recovery [(IU/dL)/(IU/kg)] | 21 | 1.42 | 1.32 to 1.59 | 0.50 | 1.76 |
| Initial half-life [h] | 21 | 7.8 | 5.4 to 9.3 | 3.0 | 36.1 |
| Terminal half-life [h] | 21 | 9.9 | 7.0 to 12.4 | 4.4 | 15.8 |
| Half-life by the noncompartmental approach [h] | 21 | 9.8 | 7.1 to 11.6 | 4.9 | 14.7 |
| AUC0-Infinity[IU*h/dL] | 21 | 1500 | 1289 to 1897 | 344 | 2437 |
| MRT [h] | 21 | 14.1 | 10.3 to 16.7 | 7.1 | 21.3 |
| Clearance [dL/kg/h] | 21 | 0.0533 | 0.0428 to 0.0792 | 0.0328 | 0.2324 |
| Volume of distribution at steady state [dL/kg] | 21 | 0.74 | 0.70 to 0.89 | 0.44 | 1.65 |
| Cmax= Maximum concentration after infusion; Tmax= Time at maximum concentration; AUC0-Infinity= Area under the curve from 0 to infinity; MRT = Mean residence time; and Incremental recovery = Maximum increase in Protein C concentration following infusion divided by dose | |||||
The protein C plasma activity was measured by chromogenic and/or clotting assay. The maximum plasma concentrations (Cmax ) and area under the plasma concentration-time curve (AUC) appeared to increase dose-linearly between 40 and 80 IU/kg. The median incremental recovery was 1.42 [(IU/dL)/(IU/kg)] after intravenous administration of CEPROTIN. The median half-lives, based on noncompartmental method, ranged from 4.9 to 14.7 hours, with a median of 9.8 hours. In patients with acute thrombosis, both the increase in protein C plasma levels as well as half-life may be considerably reduced. No formal study or analysis has been performed to evaluate the effect of covariates such as race and gender on the pharmacokinetics of CEPROTIN.
The pharmacokinetic profile in pediatric patients has not been formally assessed. Limited data suggest that the pharmacokinetics of CEPROTIN may be different between very young children and adults. The systemic exposure (Cmax and AUC) may be considerably reduced due to a faster clearance, a larger volume of distribution, and/or a shorter half-life of protein C in very young children than in older subjects. Consider this fact when a dosing regimen for children is determined. Doses should be individualized based upon protein C activity levels. see DOSAGE AND ADMINISTRATION: Protein C Activity Monitoring.
Cardio-respiratory studies performed in dogs evaluating mean arterial pressure, cardiac output, systemic vascular resistance, heart rate, QT interval changes, pulmonary artery pressure, respiratory rate and respiratory minute volume demonstrated no adverse effects at a maximum dose of 500 IU/kg.
Anaphylactoid reactions as determined by measurement of bronchospastic activity in guinea pigs demonstrated no adverse effects at the maximum dose of 300 IU/kg. Thrombogenic potential was evaluated in rabbits using the Wessler stasis model and demonstrated no adverse effects at 200 IU/kg.
Overall, safety pharmacology studies evaluating cardio-respiratory function, acute dose anaphylactoid potential and thrombogenicity demonstrated no adverse effects in a range of doses from 1.6 to 4.2 times the maximum single human dosage per kilogram body weight.
Toxicity testing in rats and mice following single dosing of 2000 IU/kg or 1500 IU/kg, respectively, demonstrated no adverse clinical effects or gross pathology at 14 days post dosing.
Studies were not conducted to evaluate repeated-dose toxicity in animals. Prior experience with CEPROTIN has suggested immunogenic response in heterologous species following repeated dosing of this human derived protein. Thus, the long-term toxicity potential of CEPROTIN following repeated dosing in animals is unknown.
Investigation of route of injection tolerance demonstrated that CEPROTIN did not result in any local reactions after intravenous, intra-arterial injections of 500 IU/kg (5 mL) and paravenous injections of 100 IU/kg (1 mL) in rabbits.
CEPROTIN contains 4.4 mg of Trisodium Citrate Dihydrate (TCD) per mL of reconstituted product. Studies in mice evaluating 1000 IU vials reconstituted with 10 mL vehicle followed by dosing at 30 mL/kg (132 mg/kg TCD) and 60 mL/kg (264 mg/kg TCD) resulted in signs of citrate toxicity (dyspnea, slowed movement, hemoperitoneum, lung and thymus hemorrhage and renal pelvis dilation).
This was a multi-center, open-label, non-randomized, phase 2/3 study in 3 parts which evaluated the safety and efficacy of CEPROTIN in subjects with severe congenital protein C deficiency for the (ondemand) treatment of acute thrombotic episodes, such as purpura fulminans (PF), warfarin-induced skin necrosis (WISN) and other thromboembolic events, and for short-term or long-term prophylaxis. Eighteen subjects (9 male and 9 female), ages ranging from 0 (newborn) to 25.7 years participated in this study.
The clinical endpoint of the study was to assess whether episodes of PF and/or other thromboembolic events were treated effectively, effectively with complications, or not treated effectively. Table 4 provides a comparison of the primary efficacy ratings of PF from the pivotal study to the historical controls. Inadequate data is available for treatment of WISN.
Table 4: Comparison of Primary Efficacy Rating of Episodes of Purpura
Fulminans in the Protein C Concentrate (Human) Pivotal Study of
Historical Controls
| Protein C Concentrate (Human) | Historical Controls | ||||
| Episode Type | Primary Efficacy Rating | N | % | N | % |
| Purpura Fulminans | Effective | 17 | 94.4 | 11 | 52.4 |
| Effective with Complication | 1 | 5.6 | 7 | 33.3 | |
| Not Effective | 0 | 0.0 | 3 | 14.3 | |
| Total | 18 | 100 | 21 | 100 | |
Of 18 episodes of PF (6 severe, 11 moderate, 1 mild) treated with CEPROTIN for the primary efficacy rating, 17 (94.4%) were rated as effective, and 1 (5.6%) was rated as effective with complications; none (0%) were rated not effective. When compared with the efficacy ratings for 21 episodes of PF (historical control group), subjects with severe congenital protein C deficiency were more effectively treated with CEPROTIN than those treated with modalities such as fresh frozen plasma or conventional anticoagulants.
Table 5 provides a summary of the secondary treatment ratings for treatment of skin lesions and other thrombotic episodes from part one of the study.
Table 5: Summary of Secondary Treatment Ratings for Treatment of
Skin Lesions and Other Thrombotic Episodes - Protein C Concentrate
(Human) Pivotal Study Part 1
| Purpura Fulminans Skin Necrosis | Other Thrombotic Events | Total | ||||||||||
| Mild | Moderate | Severe | Total | Total | ||||||||
| Rating Category | N | % | N | % | N | % | N | % | N | % | N | % |
| Excellent | 1 | 5.6 | 7 | 38.9 | 5 | 27.8 | 13 | 72.2 | 4 | 80.0 | 17 | 73.9 |
| Good | 0 | 0.0 | 4 | 22.2 | 0 | 0.0 | 4 | 22.2 | 1 | 20.0 | 5 | 21.7 |
| Fair | 0 | 0.0 | 0 | 0.0 | 1 | 5.6 | 1 | 5.6 | 0 | 0 | 1 | 4.3 |
| Total | 1 | 5.6 | 11 | 61.1 | 6 | 33.3 | 18 | 100.0 | 5 | 100.0 | 23 | 100.0 |
| N = Number of episodes | ||||||||||||
In a secondary efficacy rating, 13 (72.2%) of the 18 episodes of PF treated with CEPROTIN were rated as excellent, 4 (22.2%) were rated as good, and 1 (5.6%) episode of severe PF was rated as fair; all were rated as effective. Four (80%) of the 5 episodes of venous thrombosis had treatment ratings of excellent, while 1 (20%) was rated as good.
CEPROTIN was also demonstrated to be effective in reducing the size and number of skin lesions. Nonnecrotic skin lesions healed over a maximum 12-day (median 4-day) period and necrotic skin lesions healed over a maximum 52-day (median 11-day) period of CEPROTIN treatment, as shown in Table 6.
Table 6: Number of Days to Complete Healing of Skin Lesions in the
Protein C Concentrate (Human) Pivotal Study
| Lesion Type | Number of Episodes (Number of Subjects ) | Mean | Median | Minimum | Maximum |
| Nonnecrotic | 16 (9 subjects) | 4.6 | 4.0 | 1 | 12 |
| Necrotic | 7 (5 subjects) | 21.1 | 11.0 | 5 | 52 |
Changes in the extent of venous thrombus were also measured for the 5 thromboembolic episodes. CEPROTIN prevented an increase in the extent of thrombus during 4 (80%) of the thromboembolic episodes by Day 3 of treatment, and 1 (20%) episode by Day 5 of treatment.
All seven of the short-term prophylaxis treatments with CEPROTIN were free of complications of PF or thromboembolic events, as shown in Table 7.
Table 7: Summary of Complications During Short Term Prophylaxis in
the Protein C Concentrate (Human) Pivotal Study
| Reason for Treatment | Number of Treatments | Presentation of Purpura Fulminans During Treatment Episodes | Thromboembolic Complications During Treatment Episode | Number of Treatments Free of Complications | |||
| N | % | N | % | N | % | ||
| Anticoagulation Therapy | 3 | 0 | 0.0 | 0 | 0.0 | 3 | 100.0 |
| Surgical Procedure | 4 | 0 | 0.0 | 0 | 0.0 | 4 | 100.0 |
| Total | 7 | 0 | 0.0 | 0 | 0.0 | 7 | 100.0 |
No episodes of PF occurred in four subjects ranging from 42 to 338 days of long-term prophylactic treatment with CEPROTIN, as shown in Table 8. When not on prophylactic treatment and receiving CEPROTIN on-demand, the same four subjects experienced a total of 13 (median of 3) episodes of PF over a range of 19 to 323 days. The time to first episode of PF after exiting from long-term prophylaxis treatment ranged from 12 to 32 days for these four subjects.
Table 8: Number and Rate of Episodes of Skin Lesions or Thrombosis for Four
Subjects Who Received Long-Term Prophylactic Treatment and Were Treated
On-Demand in the Protein C Concentrate (Human) Pivotal Study
| Summary Statistic | Long-Term Prophylactic Treatment | While On-Demand* | Time to First Episode After Existing Long Term Prophylaxis | ||||
| Number of Episodes per Subject | Number of Days Receiving Prophylactic Treatment | Monthly Rate of Episodes | Number of Episodes per Subject | Number of Days Not Receiving Study Drug | Monthly Rate of Episodes | ||
| Mean | 0 | 229 | 0.0 | 3.3 | 165 | 1.91 | 23.3 |
| Median | 0 | 268 | 0.0 | 3.0 | 159 | 0.49 | 24.5 |
| Minimum | 0 | 42 | 0.0 | 1.0 | 19 | 0.25 | 12.0 |
| Maximum | 0 | 338 | 0.0 | 6.0 | 323 | 6.40 | 32.0 |
| * Total number of episodes while subjects were On-Demand was 13 | |||||||
A retrospective study to capture dosing information and treatment outcome data in subjects with severe congenital protein C deficiency who were treated with CEPROTIN under an emergency use IND was also conducted. Eleven subjects (6 male and 5 female), ages ranging from 2.1 to 23.8 years participated in this study.
There were 28 acute episodes of PF/WISN and vascular thrombus reported in which time to resolution ranged from 0 to 46 days. The treatment outcome for these episodes was rated effective in all cases except one.
CEPROTIN
[Protein C Concentrate (Human)]
Pronounced: see PRO ten
Please read this leaflet carefully before using CEPROTIN [Protein C Concentrate (Human)]. This leaflet is based on the information provided to your doctor, and is a summary of the important information you need to know about your medicine for your severe congenital Protein C deficiency. This leaflet does not take the place of talking with your doctor and does not contain all of the information available about CEPROTIN.
Use this leaflet only after you have received instructions from your doctor. If you have any questions after reading this leaflet, ask your doctor or pharmacist.
The name of your medicine is CEPROTIN, pronounced "see PRO ten". CEPROTIN contains Protein C, a natural protein that is made in the liver and is present in your blood. Protein C is a part of human plasma that regulates the blood clotting (coagulation) system and prevents abnormal clot formation (thrombosis). Plasma is the liquid part of human blood.
CEPROTIN is used to treat patients with Severe Congenital Protein C Deficiency for the prevention and treatment of:
CEPROTIN temporarily raises the levels of Protein C in the body. Protein C plays a major role in preventing your body from forming too many blood clots. CEPROTIN is for those patients who either don't produce enough Protein C or whose Protein C doesn't work correctly. CEPROTIN allows your body's blood clotting process to function properly.
Do not use CEPROTIN unless your doctor confirms that you have severe congenital Protein C deficiency.
Tell your doctor about all your medical conditions.
Allergic to Mouse Protein or Heparin:
If you are known to have allergic-type reactions (rash, hives, itching, tightness of the chest, difficulty breathing, throat tightness, and low blood pressure) to mouse protein or to heparin, talk to your doctor before using this product. CEPROTIN contains small amounts of heparin and/or mouse protein as a result of the manufacturing process.
Low Sodium Diet/Kidney Impairment:
Talk with your doctor before using CEPROTIN if you are on a low sodium diet or have problems with your kidney, as the amount of sodium in the maximum daily dose of CEPROTIN exceeds 200 mg.
Pregnancy or Breast-feeding:
Inform your doctor if you are pregnant or breast-feeding. Your doctor will decide if CEPROTIN may be used during pregnancy and/or breast-feeding.
Tell your doctor about all the medicines you are taking including prescription and nonprescription medicines, vitamins, and herbal supplements. Tell your doctor if you are on a special diet.
You could have an allergic reaction to CEPROTIN. You should be aware of the early signs of allergic reactions. These include: rash, hives, itching, tightness of the chest, difficulty breathing, throat tightness, and low blood pressure. The signs and symptoms of low blood pressure can include a weak pulse, feeling lightheaded or dizzy when you stand, and possibly shortness of breath. If you experience any of these symptoms while being treated with CEPROTIN, stop the treatment and contact your doctor. If you experience a severe allergic reaction, including difficulty breathing and (near) fainting, seek emergency treatment.
You could get an infectious disease since this drug product is made from human plasma. However, there are steps in the collection of the plasma and in the making of CEPROTIN to lessen this possibility. For example, blood and plasma donors are screened for certain viral infections. There are also steps in the processing of the plasma that can inactivate or remove viruses.
Like all medicines, CEPROTIN can cause side effects, although not everyone gets them. The common side effects to CEPROTIN observed in clinical trials were the following hypersensitivity or allergic reactions: lightheadedness and itching and rash.
There have also been individual reports, after the drug was marketed, of restlessness, increased sweating and injection site reaction.
If you develop any side effects, including any not listed in this leaflet, please contact your doctor.
CEPROTIN is given by intravenous administration (infusion into a vein). It is given to you under the close supervision of your doctor who is experienced in replacement therapy of coagulation factors/inhibitors and where monitoring of protein C activity is possible. Your dosage will vary depending upon your condition, your age and your body weight. Your doctor may require that you have blood taken to help determine the dose of CEPROTIN that you should get. See following Instructions for Use.
Store CEPROTIN in powder form, without the diluent (Sterile Water for Injection) added. Store CEPROTIN in the refrigerator at 2°C to 8°C (36°F to 46°F). Store the vial in the original carton to protect it from light. Do not freeze in order to prevent damage to the diluent vial.
Do not use CEPROTIN beyond the expiration date printed on the CEPROTIN vial.
Active ingredient: human Protein C
Other ingredients: human albumin, sodium chloride and trisodium citrate dihydrate
CEPROTIN is a white or cream colored powder that is mixed with the water provided in the package (Sterile Water for Injection) before injection. After mixing with the Sterile Water for Injection, the solution is colorless to slightly yellowish and clear to slightly opalescent and free from visible particles.
CEPROTIN comes in the following strengths:
BLUE BAR: Approximate dosage strength of 500 IU per vial.
GREEN BAR: Approximate dosage strength of 1000 IU per vial.
One package of CEPROTIN contains one vial of CEPROTIN powder, one vial of Sterile Water for Injection (diluent), one double-ended transfer needle, one filter needle, one full prescribing physician insert and one patient package insert.
Baxalta Customer Service: 1-888-237-7684
Product website: www.ceprotin.com
INSTRUCTIONS FOR USE
CEPROTIN
Protein C Concentrate (Human)
(For intravenous use only)
IMPORTANT: Contact your doctor if you experience any problems with this procedure. These instructions are intended only as an aid for those patients who have been instructed by their doctor on the proper way to self-infuse the product. Do not attempt to self-infuse unless you have been taught how by your doctor.
