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Tell the FDA What You Think, Through Comments or Public Meeting

Image courtesy of imagerymajestic at FreeDigitalPhotos.net

by Jody Smith

The Food and Drug Administration has deemed ME/CFS to be one of 39 conditions that may receive their special consideration. But of these 39, only 20 conditions will be picked. If ME/CFS is one of those 20, patients’ comments will be heard through public meetings and through mailed and emailed messages.

The FDA evaluates and approves drugs before they can be put on the market. They may also create incentives that will encourage companies to turn their focus to ME/CFS.

The FDA is holding a public meeting and is looking for input from ME/CFS patients about the FDA’s patient-focused drug development initiative. The goal is to hear patient perspectives on various conditions. The FDA is interested in knowing what symptoms patients deal with as well as how effective the available treatments are for the condition.

MC/CFS is one of the conditions on the preliminary list of nominated disease areas for this initiative, that may potentially be visited at a future public meeting. The FDA invites comments through a public docket and at a public meeting.

Public meetings will be conducted to talk about such matters as the condition’s impact on the patient and the severity of symptoms. Patients are asked to communicate what matters to them most. They are asked to evaluate how adequate the present treatment alternatives are for them.

You can also contact the FDA and share your story by mail or email. You have until November 1, 2012 to let the FDA know your thoughts.

What should you tell them? Whatever is important to you.

Describe the effects of ME/CFS on your health. Let them know what types of treatments have helped or hurt you, or did nothing for you. Pass on the names of doctors and researchers that have been beneficial to ME/CFS. Whatever is on your mind, whatever your biggest concerns, fears or hopes are, let your voice be heard.

People from outside of the United States are welcome to comment.

Write to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. Be sure to include the docket number FDA-2012-N-0967. Submit your comments at http://www.regulations.gov/#!docketDetail;D=FDA-2012-N-0967

Time is running short if you want to attend the public meeting. It will be held Oct. 25, 2012. You must be registered by Oct. 18, 2012.

The meeting will be held at the FDA White Oak Campus, 10903 New Hampshire Ave., Bldg. 31 Conference Center, the Great Room (Rm. 1503), Silver Spring, MD 20993-0002. To register, send an email to PatientFocused@fda.hhs.gov with your contact information. Include your name, title, affiliation, address, email address and phone number.

It costs nothing to register, but space may be limited. Your registration will be confirmed.

To learn more, contact Andrea Tan or Robert Yetter.

Andrea Tan can be reached at the Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 51, Rm. 1168, Silver Spring, MD 20993, 301-796-7641, FAX: 301-847-8443. You can email her at Andrea.Tan@fda.hhs.gov

You can reach Robert Yetter at the Center for Biologics Evaluation and Research (HFM-25), 1401 Rockville Pike, Suite 200N, Rockville, MD 20852-1448, 301-827-0373.

Sources:

Prescription Drug User Fee Act Patient-Focused Drug Development; Public Meeting and Request for Comments:
https://www.federalregister.gov/articles/2012/09/24/2012-23454/prescription-drug-user-fee-act-patient-focused-drug-development-public-meeting-and-request-for

{ 25 comments… add one }

  • K2 for Hope October 16, 2012, 6:13 pm

    Thanks, Jody.

    So, all we have to do is contact them via email and let them know our "stories", in a shortened version for most of us…

    And let them know why ME/CFS should get "special attention" especially in the FDA world where there is little for patients except ultra expensive medications.

    I'm in! (Thanks)

  • SpecialK82 October 16, 2012, 7:00 pm

    Done – hope everyone just takes a moment to do this. Even if you don't have the energy to write much – just say – "Please select Chronic Fatigue Syndrome!" in the comment section – let's flood them with responses.

  • Jody October 16, 2012, 8:00 pm
    K2 for Hope

    Thanks, Jody.

    So, all we have to do is contact them via email and let them know our "stories", in a shortened version for most of us…

    And let them know why ME/CFS should get "special attention" especially in the FDA world where there is little for patients except ultra expensive medications.

    I'm in! (Thanks)

    K2 for Hope,

    That's my understanding. Not a bad deal. :)

  • Omar88 October 16, 2012, 11:30 pm

    Help me am not sure how to do it !!

  • HowToEscape? October 16, 2012, 11:37 pm

    I think we need to set out a list of common themes – *not* to send a copy/pasted list of complaints, but to help cut through brain fog while composing messages. 18 hours is not enough for most of us to get 3 hours of clear writing.

    Anyone capable of proofreading and editing here? I could have done that before I got hit, not now.

  • Hope123 October 17, 2012, 12:43 am
    HowToEscape?

    I think we need to set out a list of common themes – *not* to send a copy/pasted list of complaints, but to help cut through brain fog while composing messages. 18 hours is not enough for most of us to get 3 hours of clear writing.

    Anyone capable of proofreading and editing here? I could have done that before I got hit, not now.

    Just to be clear:

    — OCTOBER 18 is the deadline if you want to attend the meeting in DC Oct. 25.

    — NOVEMBER 1 is the deadline if you want to SUBMIT comments to the FDA. So there is a little over 2 weeks to submit comments.

  • SpecialK82 October 17, 2012, 9:07 am
    Omar88

    Help me am not sure how to do it !!

    Omar, just need to follow link below, then click the blue "Comment Now!" box. Add your personal information and your comment, it can be as short as you want it to be, just make sure to ask that Chronic Fatigue Syndrome (that's what name they use) is selected for special consideration.

    * please note that all comments will be viewable by the public

    http://www.regulations.gov/#!docketDetail;D=FDA-2012-N-0967

  • anniekim October 17, 2012, 10:27 am

    Which category is it in? Many thanks

  • Nielk October 17, 2012, 10:41 am

    When I go to the page it says that 249 comments have been received but when I press "view all" it only shows 24 comments?

  • Jody October 17, 2012, 8:09 pm
    anniekim

    Which category is it in? Many thanks

    Anniekim,

    I'm not sure I understand your question. Which category where, is what in? :)

  • Jody October 17, 2012, 8:11 pm
    Nielk

    When I go to the page it says that 249 comments have been received but when I press "view all" it only shows 24 comments?

    I saw that too, Nielk. I don't know what it means either.

    Maybe someone else knows the answer to that?

  • Timaca October 17, 2012, 9:20 pm

    The problem is that the FDA cannot develop a drug for CFS/ME because there is no understanding as to what is causing the illness. More research needs to go into finding the cause(s) of the condition before drugs can be made to treat the condition…. Just my 2 cents as I looked over the FDA website….

  • SpecialK82 October 18, 2012, 8:29 am
    anniekim

    Which category is it in? Many thanks

    For Category – I used the drop down menu next to it and scrolled to the bottom and it says "Individual Consumer", that is what I picked.

    Also, it won't submit the Comment if the "Organization" field is blank, so I wrote in "none".

  • anniekim October 18, 2012, 9:12 am
    Jody

    Anniekim,

    I'm not sure I understand your question. Which category where, is what in? :)

    When I submit my comment on the left hand side there is a bar where I have to choose which category i want to submit my comment to. Many thanks

  • anniekim October 18, 2012, 9:13 am
    SpecialK82

    For Category – I used the drop down menu next to it and scrolled to the bottom and it says "Individual Consumer", that is what I picked.

    Also, it won't submit the Comment if the "Organization" field is blank, so I wrote in "none".

    Ah, great, thanks

  • Nielk October 18, 2012, 11:23 am
    Timaca

    The problem is that the FDA cannot develop a drug for CFS/ME because there is no understanding as to what is causing the illness. More research needs to go into finding the cause(s) of the condition before drugs can be made to treat the condition…. Just my 2 cents as I looked over the FDA website….

    Timaca,

    Many conditions without known causes have FDA approved drugs to treat them. For example: Migraines, Crohn's, Fibromyalgia, MS….and many more.

  • Bob October 18, 2012, 11:49 am

    This seems to be the FDA's CFS webpage, in case it hasn't already been posted:
    http://www.fda.gov/Drugs/NewsEvents/ucm319188.htm

  • medfeb October 18, 2012, 6:46 pm

    HowToEscape

    You asked about common themes. Not sure if it helps but the FDA has a set of criteria that they are using to select the disease areas.

    • Disease areas that are chronic, symptomatic, or affect functioning and activities of daily living
    • Disease areas that reflect a range of severity
    • Disease areas for which aspects of the disease are not formally captured in clinical trials
    • Disease areas that have a severe impact on identifiable subpopulations (such as children or the elderly)
    • Disease areas that represent a broad range in terms of size of the affected population
    • Disease areas for which there are currently no therapies or very few therapies, or the available therapies do not directly affect how a patient feels, functions, or survives.

    I found it helpful to keep these in mind in writing my comment

  • Timaca October 18, 2012, 7:38 pm

    OK…..comment posted. :)

    Timaca

  • Sing October 19, 2012, 8:48 am

    Lengthy comment posted.

  • Sasha October 19, 2012, 10:25 am

    Done. Thanks for posting this, Jody.

    UK people – we can take part! Anyone anywhere in the world can.

  • Jody October 19, 2012, 12:00 pm

    You're welcome, Sasha. :)

  • Nielk October 21, 2012, 10:55 am

    I just sent in my comment.

    I think it takes a couple of weeks for the comment to publicly appear. They first have to approved.

  • Nielk October 25, 2012, 10:33 am

    You have until No. 1st, 2012 to submit your comment at: http://www.regulations.gov/#!docketDetail;D=FDA-2012-N-0967

  • Anne LiConti October 29, 2012, 1:04 am

    Hmmmmm, I have a beef with the FDA as well as the CDC, not sure if my comments will be very cordial (im being nice about this). They have ignored us long enough!