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| Return to: PLEGRIDY (pegylated interferon beta-1a) | |
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| #Post#: 623-------------------------------------------------- | |
| PLEGRIDY approved for RRMS by Scottish Medicines Consortium | |
| By: agate Date: January 18, 2015, 11:08 pm | |
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| From Medical News Today, January 15, 2015: | |
| [quote]PLEGRIDY (peginterferon beta-1a) receives SMC approval | |
| for the treatment of relapsing remitting multiple sclerosis | |
| PLEGRIDY� (peginterferon beta-1a) has been approved by the | |
| Scottish Medicines Consortium (SMC) as a treatment for adults | |
| with relapsing- remitting multiple sclerosis (RRMS). | |
| Peginterferon beta-1a is the only approved pegylated treatment | |
| for MS. Utilising the pegylation process allows patients to | |
| receive the benefits of an interferon treatment with fewer | |
| injections, which may be an attractive option for patients with | |
| RRMS seeking such a benefit. Less frequent dosing is one of the | |
| factors which have been associated with improved adherence to | |
| disease- modifying therapies in patients with | |
| relapsing-remitting multiple sclerosis. | |
| As well as pegylation allowing less frequent dosing, it also | |
| allows peginterferon beta-1a to be stored outside a refrigerator | |
| at room temperature (up to 25�C) for up to 30 days (but it must | |
| be kept away from light) offering flexibility to patients in | |
| terms of how they store their medication. | |
| Peginterferon beta-1a has demonstrated an efficacy and safety | |
| profile consistent with the established interferon class. It is | |
| dosed fortnightly and is administered subcutaneously with the | |
| PLEGRIDY PEN, a new, ready-to-use autoinjector. Other disease | |
| modifying treatments for multiple sclerosis are dosed between | |
| one and seven times a week.4 Data from patients treated up to 2 | |
| years with peginterferon beta-1a suggests that less than 1% | |
| (5/715) developed persistent- neutralising antibodies (which can | |
| reduce clinical efficacy) to the interferon beta-1a portion of | |
| peginterferon beta-1a. | |
| Dr James Overell, Consultant neurologist, South General | |
| Hospital, Glasgow said, "PLEGRIDY offers a strong efficacy and | |
| safety profile, with the additional benefits of a fortnightly | |
| dosing schedule and a convenient method of administration where | |
| patients don't need to see the needle. | |
| It represents a suitable option for appropriate newly diagnosed | |
| patients or patients with tolerability and compliance issues | |
| considering a switch from other injectable or oral agents." | |
| The SMC approval of peginterferon beta-1a is based on results | |
| from one of the largest pivotal studies of a beta interferon | |
| conducted, ADVANCE5, which involved more than 1,500 patients | |
| with RRMS. | |
| In the ADVANCE clinical trial, peginterferon beta-1a, dosed once | |
| every two weeks, significantly reduced annualised relapse rate | |
| (ARR) at one year by 36 percent compared to placebo (p=0.0007). | |
| Peginterferon beta-1a reduced the risk of sustained disability | |
| progression confirmed at twelve weeks by 38 percent (p=0.0383) | |
| and at twenty four weeks by 54 percent (p=0.0069, post-hoc | |
| analysis). In addition, the number of gadolinium-enhancing [Gd+] | |
| lesions was significantly reduced by 86 percent (p<0.0001) | |
| compared to placebo. | |
| Results over two years of ADVANCE confirm that its efficacy was | |
| maintained beyond the placebo-controlled first year of the | |
| study. | |
| "Biogen Idec wholeheartedly welcomes the SMC decision" said | |
| Terry O' Regan, Vice President and Managing Director of Biogen | |
| Idec in the UK & Ireland. "We are committed to improving the | |
| lives of people with MS by developing innovative therapies and | |
| providing greater choice and flexibility in terms of disease | |
| management. Today's recommendation for Plegridy is supportive of | |
| this aspiration." | |
| The safety and tolerability profile of peginterferon beta-1a | |
| observed in ADVANCE was consistent with that of established MS | |
| interferon therapies. The most commonly reported adverse drug | |
| reactions with peginterferon beta-1a treatment (incidence | |
| ≥10% and at least 2% more frequent on peginterferon | |
| beta-1a than on placebo) were injection site reaction, flu-like | |
| illness, fever, headache, muscle pain, chills, injection site | |
| pain, weakness, injection site itching, and joint pain. | |
| Peginterferon beta-1a is the fifth therapy to be offered by | |
| Biogen Idec to people living with MS, expanding on a | |
| comprehensive portfolio that addresses individual patient needs | |
| at every stage of their disease. | |
| About PLEGRIDY (peginterferon beta-1a) | |
| Peginterferon beta-1a is a subcutaneous injectable therapy for | |
| RRMS, in which interferon beta- 1a is pegylated to permit a less | |
| frequent dosing schedule. It is a pegylated interferon beta-1a. | |
| According to the Summary of Product Characteristics (SmPC), the | |
| recommended starting dose of peginterferon beta-1a is 63 | |
| micrograms at dose 1, increasing to 94 micrograms at dose 2, | |
| reaching the full dose of 125 micrograms by dose 3 and | |
| continuing with the full dose (125 micrograms) every 2 weeks | |
| thereafter. | |
| The safety and tolerability profile of peginterferon beta-1a | |
| observed in ADVANCE was consistent with that of established MS | |
| interferon therapies. It should be administered with caution to | |
| patients with previous depressive disorders, seizures, severe | |
| hepatic impairment and In addition, the EU SmPC indicates that | |
| the use of interferon beta products is associated with cases of | |
| nephrotic syndrome, thrombotic microangiopathy manifested as | |
| thrombotic thrombocytopenic purpura (TTP) or haemolytic uraemic | |
| syndrome (HUS), hyper and hypothyroidism, hepatitis, autoimmune | |
| hepatitis, rare cases of severe hepatic failure, and decreased | |
| peripheral blood counts, including rare pancytopenia. | |
| About Pegylation | |
| Pegylation prolongs the circulation time of the molecule in the | |
| body by increasing its size, thus enabling a longer half-life, | |
| stabilising the molecule by improving its solubility and | |
| shielding the molecule from enzymes in the body that try to | |
| break it down into smaller particles. Pegylation is a | |
| well-established scientific process for medicinal use. | |
| [/quote] [References omitted] | |
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