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Conditions > Juvenile Arthritis > Juvenile Arthritis Treatment > New Juvenile Arthritis Treatment
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New Juvenile Arthritis Therapies

Adalimumab, Abatacept receive FDA approval for kids

By Robin Yamakawa

Children with juvenile arthritis now have two more FDA-approved options when it comes to exploring treatment choices. The biologic medications adalimumab (Humira) and abatacept (Orencia) were approved by the FDA back to back in February and April of 2008, respectively.

Adalimumab, an anti-TNF agent, was approved for use as a treatment to reduce the signs and symptoms of moderately to severely active polyarticular juvenile idiopathic arthritis (JIA) inpatients 4 years of age and older. Abatacept was approved for use to reduce signs and symptoms in children and adolescents 6 years of age and older with moderate to severe polyarticular juvenile idiopathic arthritis (JIA).

“To have two medications approved weeks apart for JRA is blockbuster,” says Dan Lovell, MD, MPH, Associate Director of the Division of Rheumatology at Cincinnati Children’s Hospital Medical Center. “In the history of drug development for juvenile arthritis we’ve only come up with one [other biologic FDA approved for children] so for these to be approved is great.”

More choice

FDA approval means wider availability of these medications, presenting new choices for kids who haven’t been able to tolerate or haven’t had success with other treatments. “There is no one biologic that works for every patient so it’s important to have options,” says Dr. Lovell.

In general, biologic therapies work at the cellular level of the immune system, changing the way inflammation in your body works. Because of these effects on the immune system, all biologic medications pose an increased risk of infection and related side effects. Different biologics work to stop inflammation through different ways, or mechanisms. Adalimumab blocks a protein involved in inflammation called TNF and abatacept adjusts the way certain T cells work.

With these approvals, Dr. Lovell says, adalimumab may become a biologic option prescribed to children before trying other biologics, or it may be a choice for children who have failed another anti-TNF medication. As Dr. Lovell explains, you can fail one anti-TNF and have success with another. In clinical trials, Dr. Lovell says, abatacept worked for a number of patients who had failed anti-TNF therapy and it seemed to be well tolerated.

Drug differences

Adalimumab

This medication is given through injections. Its approval was based on data from a study of 171 children age 4 to 17 that had active moderate to severe disease despite previous treatment with multiple medications. In the 48-week study, fewer children treated with adalimumab experienced disease flare compared to placebo.

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Eddie Tineo
09 Sep 2011, 04:21
My daughter Juliana will be 3yrs old on October 31 st. She is on nabumetone at the present time , at first it seem the medication was working . Unfortunately it hasn't had the effect we had hoped for. Now our has recommended Humera injections. This has me very worried because from my understanding it has only been around since 2008. What is the long term effects these meeds have on our children. But, the scariest of them what if we don't believe in science. I also am interested in any natural or organic alternatives that may helpful.
Ashley
26 Nov 2010, 08:41
my daughter is 10 and just started humira about 2 mos ago and we had to take her off her nsaids because of the reaction of humira and the nsaids were leaving white lines on the inside of her mouth and was waking up with sore from unknown reasonings..hopefully sumthing works soon...
Brittany
21 May 2010, 10:10
2010 Juvenile Arthritis Conference is July 29-August 1 in Philadelphia.

To find out additional information or to sign up for the conference go to http://www.arthritis.org/2010-ja-conference.php !
Leroy
20 Apr 2010, 13:29
My daughter was diagnosed with JRA when she was 7 yrs old, she has just turned 14. It was horrible at the onset, to the point she was in the hospital for about 2 weeks before they finally diagnosed her! She was on a drip feed of prednisone to stop the pain, and then finally we started in on alternative medicines to combat the JRA. We spent about 4 years trying various drugs, mostly injectables, but have been on once a week dose of methotreate 20mg. Good news is that she is in "clinical remission," meaning as long as she continues the meds, she does fine. She has residual damage to her ankles, where she has lost cartlidge. So it is painful when she walks too much, and cannot do any "high impact" activities. They've told us that joint replacement is not an option until she is older, so we carry on the best we can. It's truely heartbreaking when you see her at her worse, but truely inspiring when she puts on a smile and finds it within herself to get through the tough days. I am soooo fortunate to have such an amazing kid, just a shame we have to deal with such a ugly, devestating disease. I love the Arthritis Foundation, their programs(we work with Northern Califorina Arthritis Foundation) have given her many opportunities to be a part of various activities and meet other children who have and are dealing with JRA.
Overall, the doctor's (UCSF) and Arthritis Foundation have been amazing in helping us deal with this disease. Thanks to all!!!
Cathy H
12 Apr 2010, 10:01
I don't want to alarm anyone who is considering putting their child on humira but I think my daughters story should be known. We put her on humira when her polyarticular JRA was not responding to NSAIDS or methotrexate (she was seven at the time). Her joints were better almost immediately although the shots caused her anxiety. About 10 mos. into the treatment I noticed scabby bumps on her scalp which after many months of treatment for ringworm it was decided that she had developed psoriasis and that it was a side effect from the Humira. This is hard to understand since Humira is also used to treat psoriasis. Even after being off the Humira for almost a year the psoriasis is still prevelant and she has lost a significant amount of hair. Cycolsporine has helped bring it under control but we are trying to get her off that also. I guess what I think people should know is that these biologic medications (enbrel, humira, etc.) are still very experimental, especially for children.
Mommyof 4inSeattle
09 Mar 2010, 22:47
My daughter has JRA. She is 7 now and was diagnosed when she was 3. After several injections that were successful we were told that her jaw was in very bad shape and that we needed to put her on Enbrel. She's been on it for over a year. She started with a .6mg dose (15Ml) and they just upped to to 25Ml..almost double. We've noticed that she's more moody and tired. She seemed to be doing fine on the old dose, but the drs raised it b/c she gained 2 pounds. This whole ordeal has been so hard and I'm really trying to used Alt. med/vitamins/diet to get her away from drugs...any similar stories or ideas?
Ailyn Costa
25 Feb 2010, 14:12
I have a child with JRA. She was diagnosed when she was 4 years old. I've only given her 500 mg of Relefen (none of that crazy medication). I juice vegetables and gives her lots of good stuff like cat's claw, DHA, multi-vitamins, garlic and ginger,.... and it is a constant job,...but my daughter is not sickly and tired. She's healthy, with mild JRA symptoms because I do what I have to do (which means to seek alternative medicines and try different things.) Yes we can help our children,...because it seems to me that there is SO MUCH doctors don't know. I don't want doctors experimenting on my child.
Michael Smith
11 Feb 2010, 11:43
This comment is to Liz Austin. Our daughter is 11 and just started Humira a month ago. So far so good, no bad side effects. We found out she had it in July 2009. We started with NSAIDs and then Methotrexate. She could not tolerate Methotrexate because it made her vomit for three days straight. We switched her to CellCept, and now have added Humira. Email me with any questions.
Sylvia
05 Feb 2010, 02:15
I've just found in the PubMed database two studies confirming that omega-3 acids have a positive effect on juvenile arthritis!!
Sylvia
04 Feb 2010, 11:07
A week ago I found that fish oil (like other sources of omega-3 acids) helps in RA, so I started to give my daughter fish oil capsules. They seem to be helpful in my opinion. I realize that RA is not the same as JA, so I'm careful to give her normal doses, which can do no harm, I think.
amie wicker
22 Jan 2010, 01:30
my five yr old bailey has systemic jra and no meds have really helped her the dr changed her meds tocyclosporine but i dont like all the side affects does any one have ANY answers please.................
Liz Austin
02 Jan 2010, 19:58
My husband and I just took our 10 year old daughter to ACH(Arkansas Children Hospital). They diagnosed her with JIA, it is truely heart breaking to see your child suffer. The Doctor suggested Humira(biologic medication). Has anyone taken this medication and what have been your experiences and any side effects. Comments would be appreciated. We need to make a decision soon, we just want to make the best one.
Thank you.
Taylor
19 Dec 2009, 12:47
If you have JRA does that mean that you have to go to a hospital all the time???? because my son has it but we dont go to the hospital or ever get injections, but he complains all the time about his neck, ankles, back, and shoulder.
maryam
03 Nov 2009, 11:39
hope god will help you all
Lori McCourt
29 Aug 2009, 08:13
My daughter goes to Riley's Childrens Hospital in Indy. They base you on your income & also have a program called Children's for special health care needs. We qualify & pay nothing. All Meds & appts & her remicade treatments are covered! Worth looking into!
Beverly
30 Mar 2009, 10:34
My Great-granddaughter has just been accepted by the Shriners organization. They will take care of my 4 yr olds JRA until she is 18. I would suggest you give them a call they are a wonderful group.
Emma Regen
27 Mar 2009, 20:25
My nephew is 8 years old and suffers terribly from JA. The problem aside from the desease is his parents can't afford meds to help manage his pain or keep the desease under control. They do the best they can but the medicine is very expensive. Are there organizations that will help assist with the cost of his medicine?

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