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Conditions > Rheumatoid Arthritis > Rheumatoid Arthritis Treatment > New RA Treatments
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New RA Treatments

What new treatments are being developed?

A growing understanding of how the immune system works and what goes awry in rheumatoid arthritis is helping scientists develop agents that interfere with or enhance certain steps of the process. Several of these agents – referred to a biologic response modifiers or biologics – are already on the market and dramatically improving the lives of many people for whom other RA therapies failed to control the disease.

    inhibit tumor necrosis factor-alpha (TNF-alpha). , a protein that causes damaging inflammation. Although there are three TNF-α inhibitors already on the market , scientists hope to develop additional agents that will require less frequent injections  or that can be taken orally.
•    block interleukin-6 (IL-6), a protein that works with TNF-alpha to cause inflammation
•    block interleukin-15 (IL-15), a protein that attaches to receptors on cells to activate inflammatory process in the joint lining
    reduce the number of inflammation-causing immune system cells called B cells. One such agent, ribuximab (Rituxan), is already approved for RA.

Researchers are also investigating the effectiveness of drugs already approved for other illnesses, such tacrolimus (Prograf), a drug developed and approved for preventing organ rejection in people who have received liver or kidney transplants; cholesterol-lowering drugs called statins; and a class of medications called bisphosphonates, used to slow bone loss in osteoporosis.

You may learn about new or potential drugs on the news, in publications such as Arthritis Today or read reports on the Internet. When you hear about a drug that has just been approved by the FDA, ask your doctor or other health professional if it is a potential treatment.

Lesley
15 Oct 2009, 12:35
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P.S. to my last post. I did not mean to disregard prednisone as a drug that can assist in treatment. It is very helpful when having flair-ups, or during the waiting period for a new drug to take effect. But, prednisone over the long term, as the only tx, can do alot more harm then good. I am a nurse, but believe me I'm with Glow, it hit me hard too, and I was scared to death. I have had RA for 18 years, and it is well managed. Linda, I had that experience with a drug not working anymore, fortunatley, you have other options today. This is not uncommon by the way. I am only 8 years away from medicare, paying for all these drugs is a scarry thought. I also have epilepsy, diagnosed 5 mths ago. my husband has a great health plan, but if that changes, I am in big trouble. I am starting to investigate options, but who knows what healthcare will look like in 1 year, let alone 8!
Lesley
15 Oct 2009, 12:15
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Please, Please, Please. Anyone who is being treated with prednisone as their only method of care, run!!! find a new doc. There is no reason for you to be in pain, and you should see a slowing of changes with the meds out there today. Go to a rheumatologist, they truly understand this elusive disease, It is very specialized. Many drugs work better when prescribed in conjunction with another. For instance I took mtx with plaquenil, I had shortness of breath, and was weak and tired all the time. However, when the dose of mtx was reduced and I used in conjunction with enbrel, I had success, and the shortness of breath and other symptoms resolved. Granted no two people react the same to medications, or a grouping of meds. But I am sure of this, you should be working with a doc who willing to try everything to get you to a place where you slow bone changes, and stop the pain! My sed rate was through the roof, I could not walk. My entire body hurt. I couldn't sleep, I couldn't,stay up. I cried all the time from the frustration and pain. I could not be the mother I wanted to be, and no one could really understand my suffering(since it took about seven years for my joints to show changes). I looked "normal" to everyone so what was the problem? RA. I have been pain free, and while I have had some significant joint changes in my hands and feet, they don't hurt! unfortunatley, some of the newer drugs were not on the market yet when the changes in my joints started to appear. I am typing now without pain. I cook, sew, work, etc. I still get tired a little more then people without RA, but I will take that! Try everything, what works for me may not work for you, doses may need to be adjusted, etc. I know that some people have stomach issues with alot of the RA drugs, I am lucky, I don't. I have my blood work every two months, and everything is great! including the liver. I am a high risk medication patient, so bloods should be drawn every two months for this reason. I will share with you what I take, but keep in mind, we all respond differently to every med. I take (enbrel 50mgs inj. weekly), (75mgs twice a day-voltaren), (500mgs twice a day.-azulfidine), (2.5mgx5 once a week mtx), no folic acid that day. I find that for me taking my enbrel the day after mtx, works the best, and taking mtx before bed, helps some with any stomach upset they might have, just a thought. It could be in my head, but it works, so I do it. (folic acid 1mg- daily. I stay hydrated and try to keep my weight down which also helps the joints. I recently had both feet operated on, it went very well, and I now have 2 feet that look and feel terrific. I will soon beable to wear regular shoes like the rest of the population. I wish you all the best on this forum, and please, you are the best advocate for yourself, no one else!
lisa
17 Sep 2009, 11:54
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I was diagnosed with the antibodies of Sjorgren's syndrome in 2004 and had full blown RA and sjorgren's by 2005. I currently take Humira (20mg) each week. I use to take Humira once every two weeks until I developed uveitis (inflamed eyeball) and my doctors up the dosage to weekly. As a result of having both ra and sjorgren's, I went on my first biological - Orencia. Although it is slow acting, after 18 months, my symptoms were worst and the pain unbearable. I stopped working last year. My rheumy switched me to Humira. We picked Humira which has a history of treating both of my conditions. I felt instance relief but then developed a pinched nerve in my neck (misdiagnosed for three weeks), then the ortho surgeon explained that persons with both RA and Sjorgren's have weaken muscle and nerve structures. Can not longer read heavy novels - strains neck and wrists. Within the past year, I have had uveitis, developed elbow nobules, had a pitched neck nerve, a bleeding vocal cord and three steroid injections (can't take prednisone - causes severe acne - still seeing derma every month for the past 13 months and iron and vitamin D deficiences. Developed dry mouth recently. I take restatis 2x/dy, aritifical tears 6x dy, biotene mouth wash, toothpaste, spray, gel and gum 4x/dy. 3 Thera tears vitamins, arava, cymbalta, ketoprofren 1x/dy and 50,000 icu of vitamin d once a week. Although I made my living typing - typing is a crap shoot - depends on how determined I am to work in pain. Eyes are shooty at best and ankles, wrists, elbows, knees and hips play who leads the parade of pain on any given day. I'm 45 year old document specialist professional who has trouble typing. I'm still waiting for my disability, both LTD through former employer and SSDI through SSA. Down to my last coins and have not had any income for over a year - leaving through savings. But guess what? We are all still here. In pain, grouchy, stiff and weary -- but still here. I'm grateful for each day and do as much as my body allows. I enjoy my home life - I've make it as comfortable as possible and surrounded myself with all the things that I love. I have found the blessing in the storm. Its understandable and easy to bemoan our fate - but that's just a part of it. Get the best rhemy you can find, ask for recommendations for other doctors and become your best advocate. Then live and enjoy. Find a passion that lifts your spirit and when you can't do it, think about ways to improve your situation. Being in pain is a given - learning to enjoy your life is the choice.
Glow
18 Aug 2009, 11:27
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I feel sad reading these posts re. RA and the trials of meds. not working, the cost of the meds. etc.
I was dx. with RA 9 yrs. ago (this month. I am an RN and inquisitive about my own health and was very scared when I rec'd. my dx.
I did a lot of research and asked the rheumy for Enbrel. My ins. (Tricare Prime) picked up the cost for a copay of 9.00/shipment of 2 boxes which lasts 2 mos.
I'm convinced that if I was not on Enbrel, I would be in a wheelchair as the RA hit me so hard 'out of the blue'. I could barely walk, couldn't turn the doorknobs in the house, could barely turn the key in the car!!!!
When I stood up, it felt like my ankle/feet bones were breaking.
OK ENOUGH ABOUT ALL THAT!!!!!!!!
I just want you to know how severe it was when diagnosed.
I take methotrexate and folic acid also (beside the wkly. inj. of Enbrel). I am pain free, able to walk ~30 mins. daily and still ride my motorcycle. I am achy when I stay in one position to long and don't have the endurance/stamina I use to have (but then again, I'm 9 yrs. older and 40# heavier).
The wgt. gain is hard to deal with-the initial fear and depression plus unable to move around caused wgt. gain and slowly I'm trying to get it off now.
I'm sad to hear of some of the problems you guys are having.
I think the key to successful treatment is to be treated by a Rheumatologist who stays up on the latest treatments/meds etc.
I almost feel guilty to post as I'm doing well and VERY GRATEFUL.
I think that trying to keep a postive attitude goes a long way.
Blessings to all.
Joyce Johnson
15 Aug 2009, 21:55
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I have had RA for 43 yrs. and osteo arthritis for about 25 yrs. I've had a number of treatments over the years. Right now i'm receiving Remicade and have been for about 5 or 6 yrs. I'm also on 5mg of prednisone. The Remicade has kept me on my feet. Other treatments would last 2yrs. and then I'd have an adverse reaction to it.Im also on meds for the osteo. I just recently had a total knee replacement the end of June. The surgeon said it was full of the RA.Never had a problem with that knee until the beginning of April.
jeff barnes
13 Aug 2009, 18:24
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i was diagnosed with r/a in 2007 .i am a43 yr. old plumber working in pain a lot. i have been on several meds.including embrel witch gave me blurred vision.i am currently on remicade ,methotrexate,5mg. of prednizone.iam still having pain too often? i am going to cgange my diet ,no red meat,no caffene,no peppers.
elsa semeu
10 Aug 2009, 16:24
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i have been diagnosed with RA 20 years ago im 55 years old.i am taking METHILPREDNISOLONE 8 mg at day.it is very powerful and stops the pain but the ra is still advancing.what other medicine shall i use to slow as much as possible the advance?
Helen
04 Aug 2009, 14:07
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I was diagnosed with RA in 1993 and have taken different doses of predisone since together with other medications at different times. I am now on 5 mg of predisone, 20 mg of plaqunil, and celebrex. I also take vitiman supplements of vitamin C, E, calicum with D, D3, moducare and xango. My husband brought home some Moducare and after about 5 days I noticed a difference. I have been taking Moducare for over 10 years. About 4 years ago my husband brought home Xango and I started taking that also. I didn't realize how much it was helping me until I decided to stop drinking it and within a couple days, I was back to drinking Xango because I felt so much better. Something to think about.
Katie
25 Jul 2009, 14:56
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I WAS DIAGNOSED WITH RA OVER 50 YEARS AGO. SINCE THEN I HAVE BEEN ON TOO MANY DRUGS TO MENTION; MOSTLY MTX. SEVEN YEARS AGO I WENT ON ENBREL AND FELT TERRIFIC. GRADUALLY THE ITCHY SKIN RASHES STARTED. THEN I BEGAN TO HAVE PAIN AND SWELLING UNDER MY ARMS MY DOCTOR TOOK ME OFF ENBREL AND I STARTED PREDISONE. AFTER 6 MONTHS MY SYMPTOMS GOT BETTER AND I WENT BACK TO ENBREL. NOW THE SIDE-EFECTS ARE BACK AGAIN. SINCE I WEIGH UNDER 100 LBS, I THINK THE DOSAGE IS TOO STRONG. WHEN WILL ENBREL COME OUT IN PILL FORM?

kathleen
20 Jul 2009, 00:07
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I am currently on 25mg methotrexate, plaquenil, and Rituxan for RA. The first infusion in August 2008 was remarkable. I was able to get out of bed, sit/stand up without pain. However, it was short lived. Had second round in March combined with course of prednisone CRP and sed rate elevated. Early June follow-up visit showed sed rate even higher so I was given cortisteroid injection. Since my diagnosis in 2003, my RA has not gone into remission. From day one it has been active. I am unable to take other biologics since my first diagnosis is MS (1997} and Enbrel, Humira, etc. are not compatible with MS.

I have not heard of simponi but am curious as to its' effectiveness and side effects.
jeanne cozine
17 Jul 2009, 16:22
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I have had RA since 2000. I have had two knee replacements, and 30 other surgeries on my hand, knees. I am 46 years old. I have been on Orencia and Rituxan. 15mgs of Prednisone remicade,Enbrel, Methotrexate Humira.

My doctor put me on a new drug, called simponi. Has anyone used this drug and how did it work for you.
R. Marie
16 Jul 2009, 15:24
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I have had RA for 20 yrs, and have been on MTX for 20 yrs without side effects,I refuse to take anything else because everything on the market treats just the symptoms. The biggest problem I have are the rheumatoid nodules, I have them removed once a year, but my elbows and fingers look like a checkerboard of scars. How does anybody else deal with them?
Janet Washburn
16 Jul 2009, 14:11
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I have had RA for 27years and have tried several things. The Remecade was a blessing but when my husband and lost his job and ins,I know longer could afford the $8000 payments. I am still on Methrotrexate and 10mg of prednisione which I have taken along with everything else. I need a knee replacement as half my knee is gone but unable to afford the surgery. I enrolled in a clinical study and am on Tocilizumab (sp)and has helped everything but the knee is still in a lot of pain and stops me from walking on it. If there is financial help out there I would love to know about it.
GOD BLESS YOU ALL AND ANYONE ELSE WITH HEALTH ISSUES. ALL I CAN SAY IS IT IS ??? TO BE SICK AT ANY AGE.
Georgia
12 Jul 2009, 20:19
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After ready everyone else's comments I really do feel that it is a crap shoot to be able to find a medication that will put our RA into remission. I was diagnosed 12/07 and have been on Methetrexate, Placqunil, since day 1. I was on Enbrel last year and in REMISSION for 6 months before I ended up in the hospital with a "mini stroke". Then the MRI showed signs of MS, along with symptoms of blurred vision, judgement and concentration problems, etc. Once I was off Enbrel for about 3 months the symptoms went away but the RA symptoms came back. In June I had my 2 infusions of Ritixan. Seems as if the pain is better but have not had any relief from the fatigue like I did with Enbrel.
Has anyone else had similar side effects with Enbrel? I am tempted to try it again since it put me in remission so quickly and completely.
carmen
12 Jul 2009, 13:44
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is ther any help for someone who has ra and having to pay for labs and meds but am getting behind with bills i have no insurance.
donita
02 Jul 2009, 17:51
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i have been diagnosed with ra interstical lung disease (that is ra growing in my lungs) i have taken alot of ra meds aravia remicade methatrexate etc i also have ostio arthritis and osteoprosis i have lost 1 1/4" in height i have had some side affects with some of the drugs but now my problem is i need help paying for my treatments i am on rituxan now and it is almost $6,000. an infusion and i have to have 2 every 4-6 months i also have to have boniva iv every 3 months i have some ins thru SSD but it only pays 80% 20% dosent sound like much but when u r on a small monthly income it can stop u from gettin the treatments i need help is there any i have to slow my ra down or get it into remission because of it growing in my lungs i am on oxygen 24/7 now my next step is a lung transplant is there any help for prescription costs?? thank u donita
Pat Hanson
21 May 2009, 09:57
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Remicade really helped with the swelling and pain, unfortunately my wonderful insurance won't cover it out of state - what can I do
Tracie
17 May 2009, 10:14
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This is for James
Embrel has a great program called quick Assist. They have been paying most of my co-pays for 2 years. The most I have paid is $75.00
1-877-777-8718
Rebecca Z
12 May 2009, 10:05
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I was reading all of your comments. I am 68 been suffering with peripheral neuropathy since 2004 and I am not a diabetic. What I had was RA and I did not know it until after I had my double fusion in November 2007. Just three weeks after this operation I was diagnosed with severe RA. Since then I have been on Embrel, then Orencia and now Rituxan. I take 15mgs of Prednisone daily. I am getting ready to take the next series of the infusion next week. I have to say that this Rituxan has made in just 5 days a huge difference in both my knees. I am almost pain free. Now I can get up off a chair and stand up without having the pain I endured before taking this medication. I just hope that this improves and gets me into remission so that I can start to work once again. I know that there are so many of you out there that are just like I am, unemployed, some of you are uninsured, having difficult times because of the economy and some of us losing our homes. But there is a light at the end of the tunnel and we all will be glowing through it.
nancy
27 Apr 2009, 05:07
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I have undifferentiated connective tissue disease with severe raynauds. Lots of pain. Will any of these drugs work for connective tissue problems?
Diana
23 Apr 2009, 08:42
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I have a comment for James...I take Humira 40 mg every two weeks. Abbott has a plan where you can call 1-888-Humira3 (486-4723) and sign up for assistance to lower your copay to as low as $5 per month. This is a huge help to me considering I'm unemployed. Humira is very similar to Enbrel so it may be possible to talk to your Rheumatologist about switching. Hope this helps you.
James
21 Apr 2009, 19:19
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I've been on Enbrel for about 3 years, 50mg per week. Nearly all the insurance plans available in my state require a 20% co-pay. The Enbrel is close to $1600.00 per month (4 injections). That makes my co-pay $300.00 per month or more. My question is "How are average folks supposed to pay that?" Is there help of any kind out there? I don't mean for low-income. I am not in that bracket but I do have other responsibilities and bills to pay. My wife and I are retired and our income will stretch only so far. I did do the step plan the insurance companies all require before they let you have what you need. In my case, the Enbrel worked great after trying many others. It is beginning to look like I will have to just suffer because I can't manage that bill for only one prescription. Why is it so high? I realize the packaging and handling is higher, but does it cost THAT much?
Carole
18 Apr 2009, 13:30
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I was diagnosed with RA 12 years ago after I turned 50. I've been on many of the RA meds. Two years ago while on Enbrel I had a severe case of shingles. My doctor said the worst she's seen in years. After having dealt with shingles I was a little afraid of going back on Enbrel. So I stopped it. My doctor then placed me on Minocin and Limbrel. Both worked ok until the beginning of this year when I found difficulty walking. I recently had my first dose of Rituxan. I can't say I notice anything different. I'm due for my second dose in two weeks. I feel I'll know more after that dose.
dorina neer
31 Mar 2009, 11:12
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I have been diagnosted with ra in 1996. For the last 10 years I had injections with Methotrexate 2.5 to 12.5mg. intramuscular from 50 mg vials "preservative free", using the solution from one vial 4 times.The pharmacy noticed the mistake after 10 years and switched me to Methotrexate with preservative. What happened durrind those years when I had several injections from the same "preservative free" vial ? Also is it intramuscular or subcutaneous ???
Shandi
24 Mar 2009, 20:51
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It really is a crap shoot. The only "biologic" I have not been on is Rituxin. Remicade, Humira, Enbrel, Orencia, Kineret, etc...all have had some horrible side effect and not worked to boot! My rheumatologist said there is another biologic coming out before too long so maybe that will be the answer. For me, my RA is not responsive to much aside from Vioxx and they took that away from me!
linda swinyer
24 Mar 2009, 16:40
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I have had ra for many years. I am currently taking remicade along with injections of Methotrexate. I believe this is no longer working for me as does my rheumatologist. I tried the initial dosage of Rituxan and did not see any improvement at all. Do you think it would be helpful to try this again as I am at a loss as to what to try next.

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