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    Early Access Program Atl1102

    Antisense Therapeutics and myTomorrows ATL1102 Early Access Program for

    Patients with Multiple Sclerosis
    Antisense Therapeutics Limited (“ANP” or “the Company”) is pleased to announce that it has signed a
    global agreement with innovative expanded access provider myTomorrows (Amsterdam, The
    Netherlands) to implement an Early Access Program (EAP) for ATL1102 for the treatment of Multiple
    Sclerosis (MS). This program will initially be established in selected countries within the European Union
    (EU) including the 4 major pharmaceutical markets in that territory.
    Early Access Programs allow biopharmaceutical companies to provide eligible patients with ethical
    access to investigational medicines for unmet medical needs within the scope of the existing early
    access legislation. Access is provided in response to physician requests where other treatments have
    been unsuccessful and no alternative or appropriate treatment options are available to these patients.
    MS is a life-long, chronic disease that progressively destroys the central nervous system (CNS). It
    affects approximately 400,000 people in Europe and more than 1 million worldwide. A significant
    number of patients fail to be adequately treated with current medicines due to efficacy, safety or
    tolerance related issues.

    ATL1102 is directed to the target VLA-4 (Very Late Antigen– 4) for the treatment of MS. The drug was

    shown to reduce MS brain lesions in a Phase II clinical trial with the data published in the medical

    journal Neurology (Limmroth, V. et al Neurology September 19, 2014).

    Subject to myTomorrows receiving the requisite regulatory approvals and support for the ATL1102 EAP
    program, ANP expects to provide ATL1102 to MS treatment centers in the EU at prices that are
    comparable to current medicines used to treat MS. Initially the focus will be on those major European
    countries where the drug would qualify for use.
    The Company plans to access an existing source of ATL1102 material for use in the EAP that, assuming
    it is of suitable quality (to be confirmed through appropriate retesting), could potentially be available
    in the 4th quarter 2015 for the commencement of the EAP.
    Under the EAP agreement, myTomorrows will perform at their cost the EAP activities including relevant
    data collection and the seeking of the EAP approvals. myTomorrows are to receive a share of EAP
    related revenue less the cost of drug and associated pass through costs including those to Isis
    Pharmaceuticals from whom ANP in-licensed ATL1102.
    Separate to this EAP agreement, ANP is seeking a partner for the on-going clinical development and
    potential commercialisation of ATL1102. In the event of future licensing revenue and sales of ATL1102,
    myTomorrows will also be entitled to a percentage of such sales and licensing revenue received by
    ANP as compensation for the services provided, but only in those countries where an EAP had been
    established.

    Antisense Therapeutics’ CEO and Managing Director Mark Diamond said
    "Antisense Therapeutics is pleased to establish this Early Access Program for ATL1102 that may help
    the lives of those suffering from MS by providing an alternate treatment option. We look forward to
    working with treating physicians and myTomorrows to make ATL1102 available to the European
    medical community”.
    myTomorrows’ Chief Business Officer, Govert Schouten, said
    “myTomorrows is an innovative early access provider with a rapid, proactive and patient-centric
    Internet-based platform to facilitate reimbursed early access to drugs like ATL1102 in the treatment
    of MS. We have developed a core expertise in this field having implemented and conducted global
    Early Access Programs and, relevant to ATL1102, having previously managed CNS-focused EAP’s. This
    is an exciting opportunity that we believe fits well with the aims of the EAP legislation and so we look
    forward to making ATL1102 available for MS patients in need of new therapeutic options.”
    Contact Information:

    Website: www.antisense.com.au

    About Antisense Therapeutics Limited
    Antisense Therapeutics Limited is an Australian publicly listed biopharmaceutical drug discovery and development company.
    Its mission is to create, develop and commercialise second generation antisense pharmaceuticals for large unmet markets.
    Antisense Therapeutics has 4 products in its development pipeline that it has in-licensed from Isis Pharmaceuticals Inc. (ISIS),
    a world leader in antisense drug development and commercialisation - ATL1102 (injection) which has successfully completed
    a Phase II efficacy and safety trial in patients with relapsing-remitting multiple sclerosis (RRMS), ATL1103 drug designed to
    block GHr production which in a Phase II clinical trial reduced blood IGF-1 levels in patients with the growth disorder
    acromegaly, ATL1102 (inhaled) which is at the pre-clinical research stage as a potential treatment for asthma and ATL1101
    a second-generation antisense drug at the pre-clinical stage being investigated as a potential treatment for cancer.
    About myTomorrows
    MyTomorrows is an online platform that is creating freedom of choice for physicians and patients with unmet medical needs
    by offering earlier access to medicines that show promising results during clinical trials, but are not officially registered yet.
    With the support of their doctors, patients who suffer from cancer, a neurological disorder, a rare disease or a severe
    depression, can have earlier access to such medicines. For more information about myTomorrows, please visit the website
    www.mytomorrows.com.
    ATL1102 background Information
    ATL1102 is a second generation antisense inhibitor of CD49d, a subunit of VLA-4 (Very Late Antigen-4). In inflammation,
    white blood cells (leukocytes) move out of the bloodstream into the inflamed tissue, for example, the Central Nervous System
    (CNS) in MS, and the lung airways in asthma. The inhibition of VLA-4 may prevent white blood cells from entering sites of
    inflammation, thereby slowing progression of the disease. Antisense inhibition of VLA-4 expression has demonstrated activity
    in a number of animal models of inflammatory disease including asthma and MS with the MS animal data having been
    published in a peer reviewed scientific journal. ATL1102 was shown by the Company to reduce MS lesions in a Phase II clinical
    trial in RRMS patients and the data has been published (Limmroth, V. et al Neurology, 2014; 83(20): 1780-1788).



    [/SIZE][/FONT][/SIZE][/FONT]
    Early access pogram slide presentation-
    http://www.asx.com.au/asxpdf/20150527/pdf/42ytkk65s7dzn4.pdf

    Scientific Paper-ATL1102 Phase II MS trial results published in NEUROLOGY
    http://www.asx.com.au/asxpdf/20140922/pdf/42sc4g2kv2283m.pdf

    Toxicology results
    http://www.asx.com.au/asxpdf/2014040...1zsbxgmlpd.pdf

    Hadnt seen any of this posted on here so I thought you guys might find it informative! Theaccess program is due o start 2nd 1/4 next year so hopefully providing another option for sufferers particulary for those with the jc virus.
    The vla4 target s exactly the same target as Tysabri but without the chance of contracting pml due to a differing method of action where the immune system is less compromised.
    Regards.
    Looking.
    Last edited by Seasha; 12-11-2015, 04:14 PM. Reason: per guideline #2

    #2
    What are peoples thoughts on this new treatment and it being as potent as Tysabri and available from early next year under the EAP?

    "ATL1102 for MS – FDA Response to Phase IIb Study Plans
    Antisense Therapeutics Limited (“ANP” or “the Company”) is pleased to announce that the US Food
    and Drug Administration (FDA) has responded affirmatively to the Company’s plan to submit a U.S.
    Investigational New Drug (IND) application for initiation of longer term Phase IIb human trials of
    ATL1102 for the treatment of Multiple Sclerosis (MS). Supportive guidance was obtained from the
    agency’s Pre-IND assessment of the development strategy for ATL1102, including plans for a Phase
    IIb study in MS patients.
    The FDA response is an important and positive step in advancing the ATL1102 MS program. As
    previously advised, ANP is seeking a pharmaceutical partner for ATL1102’s further development.
    Antisense Therapeutics’ CEO and Managing Director Mark Diamond said:
    “The FDA Response is an excellent outcome and important step in moving ATL1102 forward into late
    stage clinical development and to capitalise on the substantial development and investment made to
    date on this key project asset. We look forward to providing further updates as we advance
    development and commercialisation plans for this exciting new therapeutic to treat MS.”
    Contact Information:
    Website: www.antisense.com.au



    ATL1102 background Information:

    ATL1102 is a second generation antisense inhibitor of CD49d, a subunit of VLA-4 (Very Late Antigen-4). In inflammation,

    white blood cells (leukocytes) move out of the bloodstream into the inflamed tissue, for example, the Central Nervous System
    (CNS) in MS, and the lung airways in asthma. The inhibition of VLA-4 may prevent white blood cells from entering sites of
    inflammation, thereby slowing progression of the disease. VLA-4 is a clinically validated target in the treatment of MS.
    Antisense inhibition of VLA-4 expression has demonstrated positive effects in a number of animal models of inflammatory
    disease including asthma and MS with the MS animal data having been published in a peer reviewed scientific journal.
    ATL1102 was shown by the Company to be highly effective in reducing MS lesions in a Phase II clinical trial in RRMS patients
    and the data has recently been published (Limmroth, V. et al Neurology September 19, 2014). The efficacy outcomes from
    this study were viewed to be as good as, if not superior to, those achieved with Tysabri® (natalizumab) the monoclonal
    antibody drug to the VLA-4 receptor, at the same 3 month time point in its clinical development. Tysabri® is linked to JC
    virus activation causing a potential lethal viral brain infection known as progressive multi focal leukoencephalopathy (PML).The
    company anticipates that ATL1102 could be as potent as Tysabri® (2013 sales - US$1.67 billion) but potentially safer (possibly

    not causing PML), cheaper to manufacturer, and more conveniently (self) administered


    In parallel, ANP’s partner, myTomorrows, is preparing a pre-registration observational study in

    Germany with the support of Professor Volker Limmroth, (MD PhD Professor of Neurology, Chairman

    Department of Neurology and Palliative Care Medicine, Cologne City Hospitals, University of Cologne)

    who was Principal Investigator of ANP’s previously conducted ATL1102 Phase IIa study. myTomorrows
    will bear costs for the observational study including the approvals process, data management and
    doctor's fees. The observational study can start as soon as patients have been supplied with product
    through the EAP which is anticipated to start in Q2’2016."

    http://www.asx.com.au/asxpdf/2014102...14vrwgwgw7.pdf

    http://www.asx.com.au/asxpdf/2015101...xtbk85pgmf.pdf
    Last edited by Seasha; 12-11-2015, 04:11 PM.

    Comment


      #3
      I think they might be getting close with a link to access and order through the program which means a whole new treatment out there.

      **URL removed by moderator in compliance with MSWorld Guidelines. This may be put in your Profile for all registered, logged-in members to see. Go to your Username on black bar running across top of page > My Settings > Edit Profile**
      Last edited by Kimba22; 12-13-2015, 02:03 AM.

      Comment


        #4
        Hi Looking and welcome. No one has replied to your thread yet, but I'm wondering what your thoughts and opinions are about ATL1102 ? Do you have RRMS and based on that, would you consider trying this new option when it's available?

        Take care~
        1st sx '89 Dx '99 w/RRMS - SP since 2010
        Administrator Message Boards/Moderator

        Comment


          #5
          Great find, Looking. All of the technical info that was posted may have confused some members, here. I know am confused by this info. But, I am encouraged by it, just the same. You know all of these MS drug companies use us, MSers, as guinea pigs. We are all drug testers for 'big pharma' !

          Comment


            #6
            Originally posted by Seasha View Post
            Hi Looking and welcome. No one has replied to your thread yet, but I'm wondering what your thoughts and opinions are about ATL1102 ? Do you have RRMS and based on that, would you consider trying this new option when it's available?

            Take care~
            Thanks for your both your replies I was a little surprised by the lack of response to what is potentially a whole new treatment out there but access to this treatment is in its early days.
            No I don't have MS but I have been following this small company's and surprised to find absolutely nothing on here re its developments as it moves towards Atl 1102's provision under the program and thought sufferers might like to know.
            The main difference between Tysabri and Atl1102 is instead of being an iv infusion , Atl1102 will be a twice weekly self administered injection and potentially safer not causing pml.
            Look I hope it is everything its meant to be and it does have someone extremely credible backing it namely Volker Limmroth (Chairman of the Department ofNeurology, Cologne General Hospital, University of Cologne, Germany.) so fingers crossed it can help sufferers.
            God knows you guys need more options and although I dont pretend to know how tough it is for all of you ,we certainly know how that feels.... to have no options....having to watch someone close lose a battle with an untreatable brain tumor at the age of 11.
            Regards
            Looking

            Comment


              #7
              Hi looking,

              I know myself, I am always suspicious when someone posts the first time without any background about themselves and their relationship to MS. Unfortunately, some people come to this and other sites and take advantage of vulnerable people.

              I am sorry for your friend's loss of a child due to a tumor. The helplessness you feel when you can't help/fix a loved one is incredibly draining.
              Kathy
              DX 01/06, currently on Tysabri

              Comment


                #8
                Originally posted by Looking View Post
                God knows you guys need more options and although I dont pretend to know how tough it is for all of you ,we certainly know how that feels.... to have no options....having to watch someone close lose a battle with an untreatable brain tumor at the age of 11.
                Hi Looking:

                Your interest is appreciated, but somehow you've gotten the wrong idea about relapsing-remitting MS, which is the form Atl1102 is intended to treat.

                RMSS doesn't have no options. There are 10 FDA-approved medications for RMSS, plus 3 more approved variations of the injectible medications. That's 13 options, plus numerous off-label medications, and stem-cell transplants, which have been successful for many recipients. That's more options than some other chronic, debilitating conditions have.

                In addition, there are other medications in the pipeline. Atl1102 is only one of them.

                And RRMS isn't like an untreatable, fatal brain tumor. Despite disability, the general life span for people with MS is only slightly below average life expectancy.

                That probably explains why one more medication in the research phase is not generating much excitement. Personally, I've heard a lot of "promising" things before, and this is just more chatter. A lot of people with MS feel the same way. I'm not going to get excited about anything that I can't get tomorrow. If Atl1102 proves to be as good as hoped, I'll cross that bridge when it comes to me.

                Comment

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