Wednesday, October 5, 2016

Nplate with Reconstitution Pack





1. Name Of The Medicinal Product



Nplate®



Nplate®


2. Qualitative And Quantitative Composition



Each vial contains 250 µg of romiplostim. After reconstitution, a deliverable volume of 0.5 ml solution contains 250 µg of romiplostim (500 µg/ml). An additional overfill is included in each vial to ensure that 250 µg of romiplostim can be delivered.



Each vial contains 500 µg of romiplostim. After reconstitution, a deliverable volume of 1 ml solution contains 500 µg of romiplostim (500 µg/ml). An additional overfill is included in each vial to ensure that 500 µg of romiplostim can be delivered.



Romiplostim is produced by recombinant DNA technology in Escherichia coli (E. coli).



For a full list of excipients, see section 6.1.



3. Pharmaceutical Form



Powder and solvent for solution for injection.



The powder is white.



The solvent is a clear colourless liquid.



4. Clinical Particulars



4.1 Therapeutic Indications



Nplate is indicated for adult chronic immune (idiopathic) thrombocytopenic purpura (ITP) splenectomised patients who are refractory to other treatments (e.g. corticosteroids, immunoglobulins).



Nplate may be considered as second line treatment for adult non-splenectomised patients where surgery is contra-indicated.



4.2 Posology And Method Of Administration



Treatment should remain under the supervision of a physician who is experienced in the treatment of haematological diseases.



Posology



Nplate should be administered once weekly as a subcutaneous injection.



Initial dose



The initial dose of romiplostim is 1 µg/kg based on actual body weight.



Dose calculation
















Initial or subsequent once weekly dose:




Weight* in kg x Dose in µg/kg = Individual patient dose in µg


 


Volume to administer:







= Amount to inject in ml




Example:




75 kg patient is initiated at 1 µg/kg of romiplostim.



The individual patient dose =



75 kg x 1 µg/kg = 75 µg



The corresponding amount of Nplate solution to inject =




 


*Actual body weight at initiation of treatment should always be used when calculating dose of romiplostim. Future dose adjustments are based on changes in platelet counts only and made in 1 µg/kg increments (see table below).


  


Dose adjustments



A subject's actual body weight at initiation of therapy should be used to calculate dose. The once weekly dose of romiplostim should be increased by increments of 1 μg/kg until the patient achieves a platelet count > 50 x 109/l. Platelet counts should be assessed weekly until a stable platelet count (> 50 x 109/l for at least 4 weeks without dose adjustment) has been achieved. Platelet counts should be assessed monthly thereafter. Do not exceed a maximum once weekly dose of 10 μg/kg.



Adjust the dose as follows:












Platelet count



(x 109/l)




Action




< 50




Increase once weekly dose by 1 μg/kg




> 150 for two consecutive weeks




Decrease once weekly dose by 1 μg/kg




> 250




Do not administer, continue to assess the platelet count weekly



After the platelet count has fallen to < 150 x 109/l, resume dosing with once weekly dose reduced by 1 μg/kg



Due to the interindividual variable platelet response, in some patients platelet count may abruptly fall below 50 x 109/l after dose reduction or treatment discontinuation. In these cases, if clinically appropriate, higher cut-off levels of platelet count for dose reduction (200 x 109/l) and treatment interruption (400 x 109/l) may be considered according to medical judgement.



A loss of response or failure to maintain a platelet response with romiplostim within the recommended dosing range should prompt a search for causative factors (see section 4.4, loss of response to romiplostim).



Treatment discontinuation



Treatment with romiplostim should be discontinued if the platelet count does not increase to a level sufficient to avoid clinically important bleeding after four weeks of romiplostim therapy at the highest weekly dose of 10 μg/kg.



Patients should be clinically evaluated periodically and continuation of treatment should be decided on an individual basis by the treating physician. The reoccurrence of thrombocytopenia is likely upon discontinuation of treatment (see section 4.4).



Method of administration



For subcutaneous use.



After reconstitution of the powder, Nplate solution for injection is administered subcutaneously. The injection volume may be very small. A syringe with graduations of 0.01 ml should be used.



For instructions on reconstitution of Nplate before administration, see section 6.6.



Elderly patients (



No overall differences in safety or efficacy have been observed in patients < 65 and



Paediatric population



Nplate is not recommended for use in children below age 18 due to insufficient data on safety or efficacy. No recommendation on a posology can be made in this population.



Hepatic Impairment



Romiplostim should not be used in patients with moderate to severe hepatic impairment (Child-Pugh score



If the use of romiplostim is deemed necessary, platelet count should be closely monitored to minimise the risk of thromboembolic complications.



Renal impairment



No formal clinical studies have been conducted in these patient populations. Nplate should be used with caution in these populations.



4.3 Contraindications



Hypersensitivity to the active substance, to any of the excipients or to E. coli derived proteins.



4.4 Special Warnings And Precautions For Use



The following special warnings and precautions have been actually observed or are potential class effects based on the pharmacological mechanism of action of thrombopoietin (TPO) receptor stimulators.



Reoccurrence of thrombocytopenia and bleeding after cessation of treatment



Thrombocytopenia is likely to reoccur upon discontinuation of treatment with romiplostim. There is an increased risk of bleeding if romiplostim treatment is discontinued in the presence of anticoagulants or anti-platelet agents. Patients should be closely monitored for a decrease in platelet count and medically managed to avoid bleeding upon discontinuation of treatment with romiplostim. It is recommended that, if treatment with romiplostim is discontinued, ITP treatment be restarted according to current treatment guidelines. Additional medical management may include cessation of anticoagulant and/or antiplatelet therapy, reversal of anticoagulation, or platelet support.



Increased bone marrow reticulin



Increased bone marrow reticulin is believed to be a result of TPO receptor stimulation, leading to an increased number of megakaryocytes in the bone marrow, which may subsequently release cytokines. Increased reticulin may be suggested by morphological changes in the peripheral blood cells and can be detected through bone marrow biopsy. Therefore, examinations for cellular morphological abnormalities using peripheral blood smear and complete blood count (CBC) prior to and during treatment with romiplostim are recommended. See section 4.8 for information on the increases of reticulin observed in romiplostim clinical trials.



If a loss of efficacy and abnormal peripheral blood smear is observed in patients, administration of romiplostim should be discontinued, a physical examination should be performed, and a bone marrow biopsy with appropriate staining for reticulin should be considered. If available, comparison to a prior bone marrow biopsy should be made. If efficacy is maintained and abnormal peripheral blood smear is observed in patients, the physician should follow appropriate clinical judgment, including consideration of a bone marrow biopsy, and the risk-benefit of romiplostim and alternative ITP treatment options should be re-assessed.



Thrombotic/thromboembolic complications



Platelet counts above the normal range present a theoretical risk for thrombotic/thromboembolic complications. The incidence of thrombotic/thromboembolic events observed in clinical trials was similar between romiplostim and placebo, and an association between these events and elevated platelet counts was not observed. Caution should be used when administering romiplostim to patients with known risk factors for thromboembolism including but not limited to inherited (e.g. Factor V Leiden) or acquired risk factors (e.g. ATIII deficiency, antiphospholipid syndrome), advanced age, patients with prolonged periods of immobilisation, malignancies, contraceptives and hormone replacement therapy, surgery/trauma, obesity and smoking.



Cases of thromboembolic events (TEEs), including portal vein thrombosis, have been reported in patients with chronic liver disease receiving romiplostim. Romiplostim should be used with caution in these populations. Dose adjustment guidelines should be followed (see section 4.2).



Progression of existing Myelodysplastic Syndromes (MDS)



A positive benefit/risk for romiplostim is only established for the treatment of thrombocytopenia associated with chronic ITP and romiplostim must not be used in other clinical conditions associated with thrombocytopenia.



The diagnosis of ITP in adults and elderly patients should have been confirmed by the exclusion of other clinical entities presenting with thrombocytopenia, in particular the diagnosis of MDS must be excluded. A bone marrow aspirate and biopsy should normally have been done over the course of the disease and treatment, particularly in patients over 60 years of age, for those with systemic symptoms or abnormal signs such as increased peripheral blast cells.



In clinical studies of treatment with romiplostim in patients with MDS, cases of transient increases in blast cell counts were observed and cases of MDS disease progression to AML were reported. Based on available data from a randomized trial, there were numerically more subjects in the romiplostim arm with disease progression to AML (placebo 2/72, romiplostim 9/147) and with an increase in circulating blasts to greater than 10% (placebo 3/72, romiplostim 25/147). Of the cases of MDS disease progression to AML that were observed, patients with RAEB-1 classification of MDS at baseline were more likely to have disease progression to AML compared to lower risk MDS.



Romiplostim must not be used for the treatment of thrombocytopenia due to MDS or any other cause of thrombocytopenia other than ITP outside of clinical trials.



Loss of response to romiplostim



A loss of response or failure to maintain a platelet response with romiplostim treatment within the recommended dosing range should prompt a search for causative factors, including immunogenicity (see section 4.8) and increased bone marrow reticulin (see above).



Effects of romiplostim on red and white blood cells



Alterations in red (decrease) and white (increase) blood cell parameters have been observed in non-clinical toxicology studies (rat and monkey) but not in ITP patients. Monitoring of these parameters should be considered in patients treated with romiplostim.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



No interaction studies have been performed. The potential interactions of romiplostim with co-administered medicinal products due to binding to plasma proteins remain unknown.



Medicinal products used in the treatment of ITP in combination with romiplostim in clinical studies included corticosteroids, danazol, and/or azathioprine, intravenous immunoglobulin (IVIG), and anti-D immunoglobulin. Platelet counts should be monitored when combining romiplostim with other medicinal products for the treatment of ITP in order to avoid platelet counts outside of the recommended range (see section 4.2).



Corticosteroids, danazol, and azathioprine use may be reduced or discontinued when given in combination with romiplostim (see section 5.1). Platelet counts should be monitored when reducing or discontinuing other ITP treatments in order to avoid platelet counts below the recommended range (see section 4.2).



4.6 Pregnancy And Lactation



Pregnancy



For romiplostim no clinical data on exposed pregnancies are available.



Studies in animals have shown reproductive toxicity, such as transplacental passage and increased foetal platelet counts in rats (see section 5.3). The potential risk for humans is unknown.



Romiplostim should not be used during pregnancy unless clearly necessary.



Breast-feeding



There are no data on excretion of romiplostim in human milk. However, excretion is likely and a risk to the suckling child cannot be excluded. A decision on whether to continue/discontinue breast-feeding or to continue/discontinue therapy with romiplostim should be made taking into account the benefit of breast-feeding to the child and the benefit of romiplostim therapy to the woman.



4.7 Effects On Ability To Drive And Use Machines



No studies on the effects on the ability to drive and use machines have been performed. However, patients should be informed that in clinical trials mild to moderate, transient bouts of dizziness were experienced by some patients, which may affect the ability to drive or use machines.



4.8 Undesirable Effects



a. Summary of the safety profile



Based on an analysis of all adult ITP patients receiving romiplostim in 4 controlled and 5 uncontrolled clinical studies, the overall subject incidence of all adverse reactions for romiplostim-treated subjects was 91.5% (248/271). The mean duration of exposure to romiplostim in this study population was 50 weeks.



b. Tabulated list of adverse reactions



Frequencies are defined as: Very common (
























































































MedDRA system organ class




Very common




Common




Uncommon




Blood and lymphatic system disorders




 



 




Bone marrow disorder*



Thrombocytopenia*




Anaemia



Aplastic anaemia



Bone marrow failure



Leukocytosis



Splenomegaly



Thrombocythaemia



Platelet count increased



Platelet count abnormal




Cardiac disorders




 



 




 



 




Myocardial infarction



Heart rate increased




Ear and labyrinth disorders



 

 


Vertigo




Eye disorders




 



 




 



 




Conjunctival haemorrhage



Accommodation disorder



Blindness



Eye disorder



Eye pruritus



Lacrimation increased



Papilloedema



Visual disturbances




Gastrointestinal disorders




 



 




Nausea



Diarrhoea



Abdominal pain



Constipation



Dyspepsia




Vomiting



Rectal haemorrhage



Breath odour



Dysphagia



Gastro-oesophageal reflux disease



Haematochezia



Mouth haemorrhage



Stomach discomfort



Stomatitis



Tooth discolouration




General disorders and administration site conditions




 



 




Fatigue



Oedema peripheral



Influenza like illness



Pain



Asthenia



Pyrexia



Chills



Injection site reaction




Injection site haemorrhage



Chest pain



Irritability



Malaise



Face oedema



Feeling hot



Feeling jittery




Hepatobiliary disorders




 



 




 



 




Portal vein thrombosis



Increase in transaminase




Infections and infestations




 



 




 



 




Influenza



Localised infection



Nasopharyngitis




Injury, poisoning and procedural complications



 


Contusion



 


Investigations




 



 




 



 




Blood pressure increased



Blood lactate dehydrogenase increased



Body temperature increased



Weight decreased



Weight increased




Metabolism and nutrition disorders




 



 




 



 




Alcohol intolerance



Anorexia



Decreased appetite



Dehydration



Gout




Musculoskeletal and connective tissue disorders




 



 




Arthralgia



Myalgia



Muscle spasms



Pain in extremity



Back pain



Bone pain




Muscle tightness



Muscular weakness



Shoulder pain



Muscle twitching




Neoplasms benign, malignant and unspecified (incl cysts and polyps)




 



 




 



 




Multiple myeloma



Myelofibrosis




Nervous system disorders




Headache




Dizziness



Migraine



Paraesthesia




Clonus



Dysgeusia



Hypoaesthesia



Hypogeusia



Neuropathy peripheral



Transverse sinus thrombosis




Psychiatric disorders




 



 




Insomnia




Depression



Abnormal dreams




Renal and urinary disorders




 



 




 



 




Protein urine present




Reproductive system and breast disorders



 

 


Vaginal haemorrhage




Respiratory, thoracic and mediastinal disorders




 



 




Pulmonary embolism*




Cough



Rhinorrhoea



Dry throat



Dyspnoea



Nasal congestion



Painful respiration




Skin and subcutaneous tissue disorders




 



 




Pruritus



Ecchymosis



Rash




Alopecia



Photosensitivity reaction



Acne



Dermatitis contact



Dry skin



Eczema



Erythema



Exfoliative rash



Hair growth abnormal



Prurigo



Purpura



Rash papular



Rash pruritic



Skin nodule



Skin odour abnormal



Urticaria




Vascular disorders




 



 




Flushing




Deep vein thrombosis



Hypotension



Peripheral embolism



Peripheral ischaemia



Phlebitis



Thrombophlebitis superficial



Thrombosis



* see section 4.4



c. Description of selected adverse reactions



In addition the reactions listed below have been deemed to be related to romiplostim treatment.



Thrombocytosis



Based on an analysis of all adult ITP patients receiving romiplostim in 4 controlled and 5 uncontrolled clinical studies, 3 events of thrombocytosis were reported, n = 271. No clinical sequelae were reported in association with the elevated platelet counts in any of the 3 subjects.



Thrombocytopenia after cessation of treatment



Based on an analysis of all adult ITP patients receiving romiplostim in 4 controlled and 5 uncontrolled clinical studies, 4 events of thrombocytopenia after cessation of treatment were reported, n = 271 (see section 4.4).



Progression of existing Myelodysplastic Syndromes (MDS)



Based on available data from a randomized clinical study in subjects with myelodysplastic syndromes (MDS), a numerical increase in cases of MDS disease progression to AML and transient increases in blast cell counts were seen in patients treated with romiplostim compared to placebo. Of the cases of MDS disease progression to AML that were observed, patients with RAEB-1 classification of MDS at baseline were more likely to have disease progression to AML compared to lower risk MDS (see section 4.4). Overall survival and AML free survival were similar to placebo. More hemorrhagic deaths were reported in the placebo arm. A reduction in the risk for clinically significant bleeding events and platelet transfusion events was seen with romiplostim treatment.



Increased bone marrow reticulin



In clinical studies, romiplostim treatment was discontinued in 4 of the 271 patients because of bone marrow reticulin deposition. In 6 additional patients reticulin was observed upon bone marrow biopsy (see section 4.4).



Immunogenicity



Clinical studies in adult ITP patients examined antibodies to romiplostim.



While 5.8% and 3.9% of the subjects were positive for developing binding antibodies to romiplostim and TPO respectively, only 2 subjects (0.4%) were positive for neutralizing antibodies to romiplostim but these antibodies did not cross react with endogenous TPO. Both subjects tested negative for neutralising antibodies to romiplostim at 4 months after the end of dosing. The incidence of pre-existing antibodies to romiplostim and TPO was 8.0% and 5.4%, respectively.



As with all therapeutic proteins, there is a potential for immunogenicity. If formation of neutralising antibodies is suspected, contact the local representative of the Marketing Authorisation Holder (see section 6 of the Package Leaflet) for antibody testing.



Adverse reactions from spontaneous reporting:



The frequency category of the adverse reactions identified from spontaneous reporting that have not been reported in clinical trials cannot be estimated (Frequency: not known). The adverse reactions identified from spontaneous reporting include:



Vascular disorders: Erythromelalgia.



4.9 Overdose



No adverse effects were seen in rats given a single dose of 1000 μg/kg or in monkeys after repeated administration of romiplostim at 500 µg/kg (100 or 50 times the maximum clinical dose of 10 µg/kg, respectively).



In the event of overdose, platelet counts may increase excessively and result in thrombotic/thromboembolic complications. If the platelet counts are excessively increased, discontinue Nplate and monitor platelet counts. Reinitiate treatment with Nplate in accordance with dosing and administration recommendations (see section 4.2).



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Pharmacotherapeutic group: Antihemorrhagics, ATC code: B02BX04



Romiplostim is an Fc-peptide fusion protein (peptibody) that signals and activates intracellular transcriptional pathways via the thrombopoietin (TPO) receptor (also known as cMpl) to increase platelet production. The peptibody molecule is comprised of a human immunoglobulin IgG1 Fc domain, with each single-chain subunit covalently linked at the C-terminus to a peptide chain containing 2 TPO receptor-binding domains.



Romiplostim has no amino acid sequence homology to endogenous TPO. In pre-clinical and clinical studies no anti-romiplostim antibodies cross reacted with endogenous TPO.



Clinical data



The safety and efficacy of romiplostim have been evaluated for up to 3 years of continuous treatment. In clinical studies, treatment with romiplostim resulted in dose-dependent increases in platelet count. Time to reach the maximum effect on platelet count is approximately 10-14 days, and is independent of the dose. After a single subcutaneous dose of 1 to 10 µg/kg romiplostim in ITP patients, the peak platelet count was 1.3 to 14.9 times greater than the baseline platelet count over a 2 to 3 week period and the response was variable among patients. The platelet counts of ITP patients who received 6 weekly doses of 1 or 3 µg/kg of romiplostim were within the range of 50 to 450 x 109/l for most patients. Of the 271 patients who received romiplostim in ITP clinical studies, 55 (20%) were age 65 and over, and 27 (10%) were 75 and over. No overall differences in safety or efficacy have been observed between older and younger patients in the placebo-controlled studies.



Results from pivotal placebo-controlled studies



The safety and efficacy of romiplostim was evaluated in two placebo-controlled, double-blind studies in adults with ITP who had completed at least one treatment prior to study entry and are representative of the entire spectrum of such ITP patients.



Study S1 (212) evaluated patients who were non-splenectomised and had an inadequate response or were intolerant to prior therapies. Patients had been diagnosed with ITP for approximately 2 years at the time of study entry. Patients had a median of 3 (range, 1 to 7) treatments for ITP prior to study entry. Prior treatments included corticosteroids (90% of all patients), immunoglobulins (76%), rituximab (29%), cytotoxic therapies (21%), danazol (11%), and azathioprine (5%). Patients had a median platelet count of 19 x 109/l at study entry.



Study S2 (105) evaluated patients who were splenectomised and continued to have thrombocytopenia. Patients had been diagnosed with ITP for approximately 8 years at the time of study entry. In addition to a splenectomy, patients had a median of 6 (range, 3 to 10) treatments for ITP prior to study entry. Prior treatments included corticosteroids (98% of all patients), immunoglobulins (97%), rituximab (71%), danazol (37%), cytotoxic therapies (68%), and azathioprine (24%). Patients had a median platelet count of 14 x 109/l at study entry.



Both studies were similarly designed. Patients (9/l) platelet counts. In both studies, efficacy was determined by an increase in the proportion of patients who achieved a durable platelet response. The median average weekly dose for splenectomised patients was 3 µg/kg and for non-splenectomised patients was 2 µg/kg.



A significantly higher proportion of patients receiving romiplostim achieved a durable platelet response compared to patients receiving placebo in both studies. Following the first 4-weeks of study romiplostim maintained platelet counts > 50 x 109/l in between 50% to 70% of patients during the 6 month treatment period in the placebo-controlled studies. In the placebo group, 0% to 7% of patients were able achieve a platelet count response during the 6 months of treatment. A summary of the key efficacy endpoints is presented below.



Summary of key efficacy results from placebo-controlled studies











































































































 


Study 1



non-splenectomised patients




Study 2



splenectomised patients




Combined



studies 1 & 2


   


 



 




romiplostim



(n = 41)




Placebo



(n = 21)




romiplostim



(n = 42)




Placebo



(n = 21)




romiplostim



(n = 83)




Placebo



(n = 42)




No. (%) patients with durable platelet responsea




25 (61%)




1 (5%)




16 (38%)




0 (0%)




41 (50%)




1 (2%)




(95% CI)




(45%, 76%)




(0%, 24%)




(24%, 54%)




(0%, 16%)




(38%, 61%)




(0%, 13%)




p-value




< 0.0001




0.0013




< 0.0001


   


No. (%) patients with overall platelet responseb




36 (88%)




3 (14%)




33 (79%)




0 (0%)




69 (83%)




3 (7%)




(95% CI)




(74%, 96%)




(3%, 36%)




(63%, 90%)




(0%, 16%)




(73%, 91%)




(2%, 20%)




p-value




< 0.0001




< 0.0001




< 0.0001


   


Mean no. weeks with platelet responsec




15




1




12




0




14




1




(SD)




3.5




7.5




7.9




0.5




7.8




2.5




p-value




< 0.0001




< 0.0001




< 0.0001


   


No. (%) patients requiring rescue therapiesd




8(20%)




13 (62%)




11 (26%)




12 (57%)




19 (23%)




25 (60%)




(95% CI)




(9%, 35%)




(38%, 82%)




(14%, 42%)




(34%, 78%)




(14%, 33%)




(43%, 74%)




p-value




0.001




0.0175




< 0.0001


   


No. (%) patients with durable platelet response with stable dosee




21 (51%)




0 (0%)




13 (31%)




0 (0%)




34 (41%)




0 (0%)

No comments:

Post a Comment