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Conditions > Rheumatoid Arthritis > Rheumatoid Arthritis News & Research > New Rheumatoid Arthritis Drug
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New Rheumatoid Arthritis Drug

By Denise Mann

When taken with methotrexate, a new pill that blocks an inflammatory protein called syk kinase may be another weapon in the ongoing war against rheumatoid arthritis (RA), finds new research presented at the American College of Rheumatology Annual Scientific Meeting.

Under development by Rigel Pharmaceuticals Inc., R788 (fostamatinib disodium) is part of a new class of rheumatoid arthritis drugs that blocks syk kinase, which can trigger the inflammation that is a hallmark of RA, thereby stopping the progression of the disease. The same agent is also being studied in other diseases, including lymphoma, lupus and type I diabetes.

In the new study of 189 people with active RA who were already taking the older disease modifying anti-rheumatic drug methotrexate, those participants who also took the 100 and 150 mg doses of the new syk kinase inhibitor twice a day showed greater improvements in their rheumatoid arthritis, than did their counterparts who took a dummy pill, or placebo. The improvement was seen as early as week one.

There were also decreases in key biomarkers of RA disease activity, including interleukin-6 and matrix metalloproteinase-3 (mmp-3) levels among people who took the 100 mg and 150 mg doses of the new rheumatoid arthritis drug. There was not a significant effect in any measure seen among people randomized to the 50 mg dose.

The new drug was also safe. The major side effects were dose related and reversible. They included diarrhea and low white blood cell count.

Unlike biologic drugs that are given by injection or infusion, this new rheumatoid arthritis drug is taken by mouth, which is a huge plus, says Eric Matteson, MD, the chairman of the rheumatology department at Mayo Clinic College of Medicine, in Rochester, Minn.

“The preliminary studies are actually very encouraging in terms of clinical effect and it is kind of exciting that they are oral,” he says. If the new findings are confirmed, the new drug and others in this class may one day be used in conjunction with biologics because they act differently. “Together with biologics, syk kinase inhibitors may be even more powerful and synergistic,” he says.

tim
07 Mar 2010, 20:12
hi I was always in pain unable to use my arms started taking the new drug and I feel great no side effects
sleeee
06 Mar 2010, 07:53
i hope it's side effects is minimum
Kamalika
15 Feb 2010, 00:37
HI,

My husband is suffering from RA from past 1 year. He is taking SAZ and Nucoxia daily. His eyes were affected but he recoverd that stage safely, but now his right leg knee in swollen heavily and his feet also.. He cant walk properly... Apart from doctors suggestion we would like to know if someone knows any other remedy that could relive some pain ...

Thanks
Kamalika
Paul
01 Feb 2010, 16:50
I am 55 and diagnosed with RA in December. So far it has been very aggresive and I am unable to continue working as a nurse. Although I appreciate it has proberbly been lurking in my system for a number of years. The onset of my RA coinsided with a swine flu jab,could this be connected ?
holly
01 Feb 2010, 16:34
i have been recently diagnosed with R.A i seem to have to take pain meds all the time is this normal daily living for me from now on ?
Joe Cocuzza
09 Jan 2010, 00:01
Hey Ricky I am 26 and had arthritis since I was 3 been in a wheel chair and got out and had my knee replaced and getting both hips replaced in Febuary.. So I feel your pain truth is My meds sometimes make my heart feel weird like its beating to fast even with little movement feels like im going to have a heart attack scary.. anyways ask your doctor if you can take baby aspirin 81mg once a day its good for the heart and maybe will releave some of your RA pain GOOD LUCK to you..Joe
Ricky
04 Jan 2010, 20:04
I have RA and have had two heart attacks
I have not been on any kind of anti inflamatory since my attacks I took viox and the doctors believe that is what contributed to my first heart attack. The second was because the stints were to small for the artery in which they were placed. My RA is full blown and I am dealing with a lot of pain is there any thing I can take that is safe for my heart.
Robin
29 Dec 2009, 12:00
Haven't had much luck with all these I.V. treatments and injections. I've taken everyone made...and have had RA since 1991. I DO NOT want to quit teaching, I love my job! My RA has worsened, but I am a fighter. If anyone knows about how to be in the trial tests for this new drug, I am so game!! I will NOT let this disease win!! EVER! Would LOVE info on this, and am printing the above to ask my Dr about. God bless all who suffer from this disease! AND I still pray others who do not have RA will come to the realization that it is not a "take some asprin and you'll feel better" kind of pain!!
linda
27 Dec 2009, 19:10
I have this learned that i have aprticularly aggresive form of RA. I also haveve figured out that a flare up of this is close to Hell on Earth! I am so glad that I am not going there because of Jesus Christ my Lord and Savior!

The Humira (an ethical treatmemnt) only worked a few months. My body won't tolerate the the Methotrexate --now I have a liver problem! I will not take the RA meds,that are derived form Aborted fetal cells! A dooctor lied to me or didn't know it when I asked about where the cells came from! I found I a site online that has a chart of ethical and unethical injections and immunizations. You would be amazed!
I am looking for natural means to get over this toxic congition!

As for the HAIR LOSS, Biotin is supposed to help that condition--- a high amount can be taken daily!
Ryan
21 Dec 2009, 14:48
I'm 29 now. I have had RA since age 24. The medications I take are methotrexate, remicade, and folic acid. The remicade made a huge huge huge difference for me. I took advantage of feeling better and being able to move more easily again. I began eating healthy and exercising. This made a huge difference. Going from 195lbs to 165lbs helps so much. If you need to loose weight try to do it. My ,feet, ankles, hips, and knees don't flare up anymore, only some random wrist/hand irritation a couple times a year(during winter??). I truly feel a healthy life style helps with RA.
Naveenchandra
08 Nov 2009, 11:40
Hi Dear Ones,

My wife is suffering from severe RA. She likes to know any new drug is available now in the market for RA so that she can be relieved of pain. Another point which I would like to mention here is that Meditation, for at least 20 minutes, daily gives a lot of relief.
Carolina
07 Nov 2009, 00:32
Hi Friends,
A neurologist gave me this suggestion for RA flareups and/or neuralgia. It really does work. (Don't use on an open wound.) It's practically free and you can avoid taking more medication when you have a flareup. Put about 10 aspirin in a small container and just cover with warm to hot water. When aspirin has dissolved completely, add hand lotion (I use Vaseline Intensive Care or unscented Aveeno)and stir until it reaches a consistency of thick cream. Spread thinly on hot, inflamed, painful areas (wrists, knees, etc.) Repeat after i/2 to one hour if needed. Keep mixture covered and stir each time you use it.
Betty
06 Oct 2009, 17:46
I was not able to see my doctor or take lab work because of past due bill. so I am on my own now. I was taking methotrexate but I have
not taken it in about a month, I have not had
any problems in fact I feel better without
the shots. I don't know if this is going to
have some effect on me later.
Joe Cocuzza
04 Oct 2009, 14:06
Hello everyone I am 26 I was diagnosed with Juvenile RA at age 3 and was placed in a wheel chair from 3-8..The meds I have taken over the years are Methotrexate, Enbrel injection,Humira injection, Orencia IV,Remicade IV, Prednisone,Relafen,Ultracet,Percoset, Oxycontin,Imitrex,Arava,about 6 advil a day when needed about 4 tylenol a day when needed many cortizone shots in several joints, NOTE: not all taken at once! just thru the years they all worked great at first then ware off..
I just had my 18th surgery June 23 09 I had a total knee replacement and am struggling with recovery. They then had to munipulate under anestesia in sept. I go to therapy 5 days a week 3 hours a day.. I have been on disability since June and now my job benefits run out as of November and have to return to work.. I now been having severe hip pain so I went to the Dr. he mentions I have avascular nacrosis where the hips don't get enough blood supply then the tissue and bone dies I will become paralyzed from the waist down if I dont get my hips replaced and at 26 replaceing my body parts isn't exactly what I want to do. I'm in a new marraige and im sure it takes a tole on my wife. although she very supportive, but its just hard because we dont go out as we use to my friends start doing there own thing singling me out because they do things I can't par take..Its sad when you see friends drift away, thats what should make us apprieciate our spouse. I know we can relate on here. we are all going thru tough times.. but by writing on this you never know who you will inspire! Its hard when you go from having alot and being able to do so much to almost losing everything and almost being able to do nothing.. I feel like im going backwards! But trust me people we have to stay as possitive as possible and believe me I know its hard! Its funny because Im sure you've heard "oh it could be worse theres people out there that are really bad or have cancer or whatever" and you feel like your being selfish because in your mind you dont care what anyone else has or going through. all you know is the pain you suffer from! Anyways Even though its hard! try to smile thru the pain keep possitive and know that there will be a better day! Take your meds, excercise,use heating pads, ice, go for a soft relaxing massage whatever it takes to help you get thru the day! talk to your Dr about everything. dont hold anything back get second opinions make smart decisions. work hard!. the funny thing is us with problems work harder then people without problems its like we have to prove something to ourselves! or you know those people on welfare that dont need it but get it anyways rather then those who really need it!! I just lost medicade that I had since I was 3 because I got married isnt that something? they combined your income well NJ does anyways.. oh well
ENJOY LIFE GOD BLESS!
Nick Palmieri
16 Sep 2009, 13:18
Lisa our daughter was diagnosed w/JRA age 4, now 17 yrs old. We started w/ Metho. (varying doseages, oral and subQ)together with Naprosyn and Folic Acid. Later progressed to Enbrael (alone)worked ok about 9-12 mos, then Humira alone w/no relief- (under Humira alone JRA progressed far back to orignal untreated diagnosis state). A blow up w/our Pediatric Rheum. to get back to Metho. due to near remission 3x over 12 yrs, we began Metho. and Enbrael with folic. OUr daughter did wonderfully w/ near imediate results. However, today we're dealing with Osteopenia inaddition to JRA, unsure whether disease, drugs long term or combo of both has created this. Either way, our point - Metho and Enbrael combo worked for us even though last appt. was her first time for Aspiration of fluid in knee. Weigh the long term saftey studies, (many published by Arthritis Foundation) and start treatment. Experimentation w/combo's and dosage is normal. JRA has no set table for all. Each person and progression appears to be different. Excersise and keep healthy diet. Not starting treatment can seriously effect ability of remission the older a patient gets.
Dani it
05 Aug 2009, 12:47
Hi everyone I was diagnose a year ago with RA but I had the first sintoms one year prior. The Reumatologist put me on Metotraxate and also on Humira.
Since I started the injection I had a noticeble improvment, but yet months later I am still in pain,and my quality of life is not that great.
It is very sad that in the year 2009 there is no cure for this condiction.
Anyway my toughs goes to everyone that does not have an insurance willing to pay for the medication or even worse insurance at all.
So I may suggest somenting that brought me some relif: Boswellia serrata (aryuvetic medicine),Tumeric (both for the inflammation) and as probably many knows the combination of glucosamine 1500 mg, chondroitin mg and msm 500mg. that it worked for me for a wile pretty good.
I hope to have been helpfull.
Meanwile i was wondering if anyone have some tips for the hair loss that I am experiencing wile taking metotraxate.
Something natural pheraps?
God bless
Alma
19 Jul 2009, 17:58
I am 45 and have RA in both hands and wrist. I have a job that takes alot of typing on the computer. I am not sure how long I can kept this job; the pain gets worst everyday I am taking every thing the doctor has given me but it just does not get any better.
Elisa
02 Jul 2009, 22:45
I was diognosed a year ago, I'm not on meds just trying alternative meds. Can you provide more info?
olga loera
02 Jul 2009, 19:51
hi im 46 years old and have lived with ra for six years lately ive been in pain and heared about this new medication i dont have insurence and med are very costly if anyone knows about a study in palmdale ca please help
Pam
20 Jun 2009, 08:09
Please tell Filomena that there is a program for Remicade through the manufacturer to help with the payments. she should ask her medical provider about either Remistart, Access 1 or Cecticor; they should be familiar with one of those names.
jane
17 Jun 2009, 17:12
what is the new drug? it was on the news last night and it is in clinical trial at Mass General in Boston. Please help
Carolyn
14 Jun 2009, 13:04
I am on methotrexiate 2.5 X 6 per week. Have been for over 15 years. Doesn't seem to work anymore. I need something fast. What about the new pill R788 ??? Has it been approved and can I now ask my Dr. about it?? I am having pain in both knees and muscle spasm's in my neck and back of head. Could this also be fibromyalgia??
Lisa
01 Jun 2009, 10:41
Hi-I have had JRA/RA since I was 13. I have been fairly well controlled on methotrexate 2.5mg X3 and now my doctor wants me to take Enbrel. Everything I read is scaring me about the drug. I feel fine-rarely have flare ups yet she said I am progressing and the joints will erode. So confused. This new drug looks good-would love to be in a study-also in Ohio.
tony
01 Jun 2009, 07:40
hello ,
i have R.a now for five years i'm 53 now , and sometimes my pain comes and last for two weeks i have heard about this new drug , i;m very interested in trying it if you know of a study in the ohio area please contact me , i would love to try to help all of the 1.3 million others with this desease, to live a better life, thanks tony
frances
08 May 2009, 07:07
my Father is 83 years old and he has RA each time I see him, he is either sitting down on a recliner with a hot water bag or a massager he says it is very painful. I like to help him but he also complaints about stomach pain and blames the medications he is taking..he has gone through CT scan to check his intestine and several test all are normal... is this medication ok to take at his age? we will consult his physican...
T. Lunt
20 Apr 2009, 03:22
I have taken Methotrexate (2.5mg x6 every Tuesday) for about 15years now, and I find that it is keeping th RA in check at the moment, yes I do have flier-ups lasting for about 2/3 days, which are very painful.
I can withstand most off the painful joints, but the only one that brings me down, is when it is in both of my jaw joints, that is very bad, but I thank my God, it only lasts for about 5/6 days.
filomena
18 Apr 2009, 21:26
Please I need help I no have insurance I need my medication is very expense is remecade on i no have de infusion I cant move please some Hospital help me plesae
bin-zayed
12 Apr 2009, 12:25
what is the latest drug for rheumatoid arthritis? can someone help?
Sharon
25 Mar 2009, 18:12
I meant rheumatologist -- I haven't seen two neurologists. But after all tests came back negative, she told me to stop the Botox, so she's clearly suspicious.
Sharon
25 Mar 2009, 18:07
Has anyone every heard of a connection between cervical Botox injections and sudden onset of RA in the hands and wrists? I have seen a terrific neurologist, a hand specialist and now have a highly respected neurologist, but repeated blood tests for everything from RA to ANA show nothing. I have been getting Botox injections in my neck for almost a year -- the hand problem started with the second three-month course -- and no one seems to know what is wrong with me. I'm at the end of my rope.
Veronica
21 Mar 2009, 13:52
This drug seems to have less risk and its oral When can we know more than this new drug?Thanks a lot
Connie
10 Mar 2009, 15:08
Yes i can't take pain meds strong enough to help me because i have a low tolance for morfine. They don't want us to take vicadon now. Pleas i'am on Medicare and Medicaid. I suppose these drugs won't be covered. Do you need people to try out the new drug. Can you help. Thank you Conne

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