I have received a lot of interest from others on here in my involvement with the Xeljanz trials at Yale.

I thought it would be nice for everyone if I documented my progress on here. 

Xeljanz is a Jak3 inhibitor and is believed to work with alopecia by turning off the distress signal relayed by the hair follicle to the attacking immune system which is the cause of the hairs falling out. Xeljanz comes in a strength of 5mg per pill and a full box contains 60 tablets. The recommended dosage for arthritis is 1 tablet in the morning and another in the evening each day.

The trial is set in a series of stages and there are requirements before participating. These include monthly visits and blood tests every 2 weeks. Dr Brett King is absolutely fantastic and is an inspiration to me. His positivity and enthusiasm gives me the much needed hope I have craved for over a decade. I have been put on a low dose to start with which is 1 tablet every other day. My dosage has now been increased to 1 tablet every day and next month it could be increased to 2 tablets per day depending on the results. 

I have completed my first month and have already noticed my alopecia has stabilised . I have not lost any existing hairs. In addition to this I have seen little hairs growing in my chest area as well as eyebrows. Fingers crossed! To date, I have experienced no side effects.

 

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I'll have to go back to my notes to see how long before we changed the dosage. He started on 15mg (2 x 5mg in the morning 1 x 5mg at night) I believe this was 3 months, we then went to 20 mg / day and he really improved. After about 9 months at 20mg we scaled it back to 15mg and for the past 4 months at 10mg. I think he will need to go back to 15mg, but we are monitoring his eyebrows. He responded rapidly so I would say it was somewhere around that 13-14 month mark where we went from 20mg down to 15mg.

My wife is concerned about the long-term potential of liver problems so we were pretty aggressive about trying to reduce the dosage. He wasn't having problems and his liver tests were fine, just being cautious. I have no issue with him going back up to 15mg if needed. I should have taken some pictures just before the reduction so we could have better measured the impact of going to 10mg.. I would recommend that.

Thank you so much for this reply, and for coming back on the website to share your son's story. This information is really helpful :)

My son is back on 15mg per day (10 in the morning 5 at night). His hair looks great we are just seeing if going back to 15mg from 10mg helps fill in his eyebrows a bit more. We did blood work before this and all tests are normal. He will keep on 15mg for 6 weeks then we will consult with the Dr. I took before pictures with a ruler so it is easier to measure success which I would recommend to others. 

Side update: my company switched to Cigna / Express Scripts this year so I have spent the past 4 months fighting for coverage. For the past year he was rejected by Aetna but given the meds for free from Pfizer / Xelsource. 

Cigna also rejected him despite his good results. We appealed the decision and actually got it approved for coverage upon appeal!! I will see if I can find a CIGNA thread and add that note. The more examples of successful appeals the harder it will be for insurance to reject it. 

Good luck to everyone.. 

Thank you, but I would keep a back up source as they can cancel at any time.

Is anyone here using the Pfizer Assistance Program?

I am using it currently, and have been for over a year, but I am worried what happens once my salary goes above their max income level for the program.

Has anyone been in this position before or knows what happens?

I can also call them, but I wanted to know before hand 

Hi everyone,

Quick update from me. I was diagnosed with AU 3 years ago. I tried Tofacitinib about 2 years ago. I was on 20mg for about 3-4 months and didn’t see any results. I ended up stopping treatment because I firmly believed that I was in the minority that didn’t respond to treatment. Fast forward to the beginning of this year, my new dermatologist recommended I start on the medication again saying that my initial treatment wasn’t long enough. This time around, I saw vellus hair growth within 2 months, terminal hair growth within 4 months and I now have 100% of my scalp hair back. My eyebrows are still very thin (probably only 20%), and the rest of my facial hair is patchy. This site is the only reason I discovered this medication so I appreciate everyone staying active and providing hope to all those going through this. 

Also, if anyone in the NYC area has extra tofacitinib supply, I would gladly pay for a few weeks worth. I am running dangerously low on my existing stock, and with all of the delivery delays from Beacon I am not sure I will get my new order in time. Message me! 

Hope everyone is staying safe and healthy. 

So glad to hear this!

Hi NYGuy, thanks for posting - it's really encouraging to hear about your experience.  Did you go back to 20mg on the second time around? And did you start on this dosage or work up to it?  I've just started using Tofacitinib from Beacon (11mg XR in the morning, 5mg at night) so curious to hear how you came to your dosage.

First time around I started at 10mg/day for about a month before bumping to 20mg for 3 months. Again, I didn’t see any results that time. Second time, I started on 10mg for about 2 weeks before jumping to 20mg. I have been on that dosage for 6 months now. 

Hows the growth on 20mg?

that’s wonderful NYguy! I know I go on and on about the time thing but honestly it can take more than 8/9 months to respond in the beginning and it’s so hard not to give up, especially if you are stuck paying the insane price for the original. After being on a reasonably high dose (20 msg) I am now on 10 mgs (11 mgs but the generic so probably 10) most days, with every third day doing 20mgs. Have done this now for about 3 months with no repercussions, which surprised me - given the world situation is a bit stressful. I decided to try reducing so my stockpile would last longer, though I do feel supply will once again open up. I guess having been on the meds now for 3 years I am an old timer, and can say for the most part I have maintained better health on the meds than off.... So glad to hear of your success!

Hi Frida , I have a question, I’m currently taking 20mg if Xeljanz with  minoxidil for about a year and a half . I noticed yesterday that I’m developing a spot and it’s totally freaking me out !! I’m scared because I had an awful flair up while being on 15mg and when we raised the dose it calmed down but know I’m on the highest dose and I’m still having a flair up . Have you had any spots being on this dose ? 
Maree

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