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First oral drug approved by FDA; Gilenya to be in pharmacies shortly

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  • First oral drug approved by FDA; Gilenya to be in pharmacies shortly

    Huge news and a relief to those needle-phobic. All details are below. - Dave

    Novartis gains FDA approval for Gilenya™, a novel first-line multiple sclerosis treatment shown to significantly reduce relapses and delay disability progression
    • Gilenya is the first approved oral treatment indicated for relapsing forms of MS in the US, a major advance for people with this disease
    • Gilenya showed superior efficacy by reducing relapses by 52% at one year compared with interferon beta-1a IM, a commonly prescribed treatment
    • Two-year, placebo-controlled study showed that Gilenya significantly reduced the risk of disability progression
    • Well-studied safety and tolerability profile with over 2,600 clinical trial patients
    East Hanover, NJ, September 22, 2010 /PRNewswire/ — Today Novartis announced that the US Food and Drug Administration (FDA) approved the oral multiple sclerosis (MS) treatment Gilenya™ (fingolimod) 0.5 mg daily, a first-line treatment for relapsing forms of multiple sclerosis – the most common forms of the disease. The FDA approval makes Gilenya the first oral treatment indicated for relapsing forms of MS available in the US.

    “Today is a significant and encouraging day for people with relapsing forms of MS in the US,” said Nicholas LaRocca, Vice President of Healthcare Delivery and Policy Research at the National Multiple Sclerosis Society. “A new treatment option that offers significant efficacy in the convenience of a capsule is a welcome alternative to frequent injections for individuals living with this chronic disease.”

    Gilenya reduces the frequency of MS relapses (flare-ups) and helps slow the build-up of some of the physical problems caused by MS. In clinical trials, Gilenya has a well-studied safety and tolerability profile, which has been characterized in over 2,600 clinical trial patients, some of whom are in their seventh year of treatment, with more than 4,500 patient years of experience.

    “Through a novel mechanism of action, Gilenya can significantly improve clinical outcomes among patients with relapsing forms of MS,” said Fred Lublin, MD, Saunders Family Professor of Neurology, The Corinne Goldsmith Dickinson Center for Multiple Sclerosis, Mount Sinai School of Medicine. “Gilenya provides significant efficacy and manageable safety when used in accordance with approved labeling, making it a valuable advancement for relapsing MS patients and the physicians who treat them.”

    The Gilenya approval was based on the largest clinical trial program ever submitted to date to the FDA for a new MS drug and included combined data from clinical studies showing significant efficacy in reducing relapses, the risk of disability progression, and the number of brain lesions detected by magnetic resonance imaging (MRI), a measure of disease activity, in people with relapsing forms of MS.

    “We are proud to have worked successfully with the MS community toward a shared goal of bringing a novel efficacious treatment to people with relapsing forms of MS,” said Trevor Mundel, MD, Global Head of Development at Novartis Pharma AG. “We are actively pursuing regulatory approval in Europe and the rest of the world.”

    Gilenya is the first in a new class of drugs called sphingosine 1-phosphate receptor (S1PR) modulators. In MS, the immune system damages the covering that protects nerve fibers in the central nervous system (CNS), which includes the brain and spinal cord. Gilenya’s novel mechanism is unknown, but it is thought to work by reducing the immune system’s attack on the CNS by retaining certain white blood cells (lymphocytes) in the lymph nodes. This prevents the white blood cells from reaching the CNS, where they could potentially attack the protective covering around the nerve fibers, resulting in less inflammatory damage to the nerve cells. The white blood cell retention is reversible if Gilenya treatment is stopped.

    About Gilenya

    Gilenya is a prescription medicine used to treat relapsing forms of MS in adults. Gilenya can decrease the number of MS flare-ups (relapses). Gilenya does not cure MS, but it can help slow the build up of physical problems that MS causes.

    The FDA regulatory application included data showing Gilenya 0.5 mg reduced relapses by 52% (P<0.001) at one year compared with interferon beta-1a IM (Avonex®), one of the most commonly prescribed treatments for MS. Gilenya also reduced disease activity as measured by the number of new and newly enlarged T2 lesions on MRI scans compared to interferon beta-1a IM (1.6 vs 2.6, respectively, P=0.002) at one year. Data from a two-year placebo-controlled study showed a reduction in relapse rate (54% reduction P<0.001, compared with placebo) and risk of disability progression among Gilenya patients (30% reduction confirmed at 3-month follow-up visit P=0.02, compared with placebo).

    In both studies, treatment with Gilenya also resulted in statistically significant reductions in brain lesion activity as measured by MRI.

    Gilenya was submitted to the European Medicines Agency (EMA) and to the US Food and Drug Administration for review in December 2009. The EMA regulatory review and other filings worldwide are ongoing.

    Gilenya Important Safety Information

    Gilenya may cause serious side effects such as slow heart rate (bradycardia or bradyarrhythmia), infections, macular edema, breathing and liver problems.

    Gilenya can cause a patient’s heart rate to slow down, especially after the first dose. The heart rate will usually slow down the most about six hours after a patient takes their first dose of Gilenya. Patients might feel dizzy or tired or be aware of a slow or irregular heartbeat if their heart rate slows down. A doctor will watch patients for the first six hours after they take the first dose to see if they have any serious side effects. A patient’s slow heart rate will usually return to normal within about one month after they start taking Gilenya. Patients should call their doctor if at any time they have dizziness, tiredness or a slow or irregular heartbeat.

    Gilenya can increase a patient’s risk of serious infections. Gilenya lowers the number of white blood cells (lymphocytes) in the blood. This will usually go back to normal within two months of stopping treatment. A patient’s doctor may perform a blood test before they start taking Gilenya. Patients should call their doctor right away if they have fever, tiredness, body aches, chills, nausea or vomiting.

    Macular edema can cause some of the same vision symptoms as an MS attack (optic neuritis). Patients may not notice any symptoms with macular edema. Macular edema usually starts in the first three to four months after taking Gilenya. A doctor should test a patient’s vision before they start taking Gilenya and three to four months after they start taking Gilenya, or any time they notice vision changes during treatment. Risk of macular edema may be higher if a patient has diabetes or has had an inflammation of the eye called uveitis. Patients should call their doctor right away if they have blurriness, shadows or a blind spot in the center of their vision, sensitivity to light or unusually colored vision.

    Some patients who take Gilenya have shortness of breath. Patients should call their doctor right away if they have trouble breathing.

    Gilenya may cause liver problems. A doctor should do blood tests to check a patient’s liver before they start taking Gilenya. Patients should call their doctor right away if they have nausea, vomiting, stomach pain, loss of appetite, tiredness, dark urine, or their skin or the whites of their eyes turn yellow.

    Gilenya may harm an unborn baby. Women should talk to their doctor if they are pregnant or planning to become pregnant. Women who can become pregnant should use effective birth control while on Gilenya and for at least two months after stopping. If a patient becomes pregnant while taking Gilenya or if they become pregnant within two months after stopping Gilenya, they should tell their doctor right away. Women who take Gilenya should not breastfeed, as it is not known if Gilenya passes into breast milk.

    Patients should tell their doctor about all their medical conditions, including if they have had or now have an irregular or abnormal heartbeat, a heart rate of less than 55 beats a minute, a fever, infection or if they are unable to fight infections, eye problems, diabetes, breathing or liver problems, or high blood pressure. Patients should especially tell their doctor if they have had chicken pox or have recently received the vaccine for chicken pox. A doctor may do a test for chicken pox virus and patients may need to get the vaccine for chicken pox and wait one month before starting Gilenya.

    Patients should tell their doctor about all the medicines they take, including medicines for heart problems or high blood pressure, vaccines, other medicines to control their immune system or treat cancer, or ketoconazole (an antifungal) by mouth.

    The most common side effects with Gilenya were headache, flu, diarrhea, back pain, abnormal liver tests and cough.

    For full prescribing information and the medication guide log onto
    Dave Bexfield

  • #2
    I am beyond excited to hear this. I plan to be an early adopter


    • #3
      It appears the cost will be $4,000 a month or $48K per month. Expensive, but cheaper than Tysabri.
      Dave Bexfield


      • #4
        Just a note, I received a call from my neuro's nurse yesterday afternoon and the drug is now available. I have an appointment on Tuesday to go fill out all of the paperwork and get orders for what I imagine will be a battery of blood tests. I have already had the mandatory eye exam checking for macular edema (I don't have that, yay!).

        I am pretty happy, as it means my neuro really took me seriously when I presented an educated case to switch me from copaxone (new active lesions, disease progression in comparison report of my MRIs) and there is no way I can remain on Copaxone for the long term. And he remembered and had her call me....YAY

        And for the most exciting thing, I get to stop taking the copaxone on Tuesday after my appointment for a 1 month wash out period. I am thrilled. No more pokes and prods, no taking my needles with me to Mexico in December.

        I'll let ya'll know how it goes. Its of course not for everyone, but its definitely for me.


        • #5
          4 weeks on Gilenya

          I have just completed my first 4 weeks of Gilenya. It is a process to get on this.
          Recap of the process:
          visit with my neurologist to discuss, sign consent forms, etc.
          Blood work
          More blood work- neuro didn't realize that a varicella titer had to be drawn even if you have a history of chicken pox
          Appointment with Dermatologist for full body survey looking for cancers
          Appointment with Ophthamologist and retinal scan
          Once all of this is accomplished, I received a call from my "nurse navigator". She reviewed the medication side effects, etc, etc. This was a long, not particularly helpful call, but it is a necessary step in the process.
          About a week later, call from my neurologist that my first 2 weeks of meds had arrived and that I had to come in for a 6 hour observation for the first dose.
          December 17th- First dose- neuro office had a small office set up with a recliner chair and that was it. I took knitting and reading. My DH brought lunch. They checked my pulse every hour. I started at 58 and dropped to 50 but no symptoms. The day was pretty easy(boring) and definitely painless. It definitely beats the injections.
          I wasn't on any treatment, so no washout period was needed.
          It seemed like a long process, but I guess it was less than 6 weeks from start to finish.
          I receive frequent calls from my nurse navigator. The drug comes from a specialty pharmacy. This is a rather cumbersome process. The calls with this pharmacy seem to take about 20 minutes each time. I am hoping this improves.
          The med comes in a 28 pill pack which is called a month supply. It isn't clear how this works as few months have just 28 days. I am trying to get 90 days supply, but so far, no luck.
          So far, I am pretty happy with the med. I have had 2 skin infections- one from a cat scratch and one from a biopsy done by the dermatologist. I am a bit worried that this is an effect of the med, but it could just be bad luck.
          I hope this helps anyone starting down this road.
          Last edited by pawpaw; 01-14-2011, 05:52 PM.