Neratinib Clinical Trials
Comments
-
Cathy
That's a good point about the new pills after each check-in. I had my 12 week follow up yesterday. The ladies on this thread no more about the latest with the trial than, I think, my coodinator! She confirmed what has been said here. But said it doesn't really affect me, since I have about 6 more months on the trial.
I asked about the diarreah and she confirmed that not everyone gets it. I told her that other women on this thread experienced SEVERE D while taking Keflex (my experience) and she kind of poo poo'd that (pardon the pun). Anyway, I have sensed some potential SE's come and go when I get the new pills. Who knows, I may end up not having gotten the drug at all. I guess at some point they will un-blind the study (possibly before FDA approval?) so we'll find out. And if the results have been good, we'll all get the drug--though I wonder if they'll give us the drug if we are more than 1 year out from Herceptin ending... -
When is this study going to end? How is is looking? I am debating whether or not to seek out this trial. To tell you the truth, I think I may just want to be done with treatment and not spend any more time in hospitals than I have to. I keep putting it off, the SERIOUSLY looking into participating. How are you all feeling?
-
Kathleen - this study has already ended to new participants. I believe Puma is going to start new trials early 2012.
So, its day 6. No side effects at all over the weekend. This morning i kicked the side of the bathtub and noticed that my toes felt "funny" as I type this i'm feeling a little bit of neurapathy in my fingers. Then...out of nowhere....loose stools!!! Just as I had lost all hope that I got the drug...hope is renewed!
-
Oh, and while i'm here - i'm trying to find out what the ingredients are of the placebo. I'm pretty sure I found something online before. Does anyone know where I could find this information?
-
Heather - if you cont to have D please call your dr. It can be difficult to control in the beginning. I had 5 days straight but I've been better since.
-
FYI: Who ever said that the mix of meds changes with each new batch of bottles you get at study visits is definitely on to something...I started a new bottle of meds yesterday, and boy, it's the worst D I've had since starting 6 mos ago (w/o taking antibiotics w/it)
Coincidence? Don't know but makes me wonder...
-
Hi ladies, yeah either way alot of it is guess work for us on the single arm Plll-study-trial, with-out existing tumors to gage shrinkage or stabilization, thankfully so.
I have also wondered about the batch changes in bottles and have been silly enough to break one in half to see if the colouring changes, stupid really ! got to slap myself sometimes.
heather I was like you and went till day 6 or 7 until the loose stools came, then with out warning whammo, big momma D had arrived, I was still not convinced, I thought, maybe the placebo has a type of sugar content that has a natural D effect on our digestive system, Im still guessing !
I think we should also keep an eye on our blood WCC count as Neratinib is a chemotherapy drug, cytotoxic ( 0.8.01 ) according to Pfizer data, so its probable to slowly have an effect on our Neutrophils as well as the fact that the food we are eating is not absorbed in time for nourishment with out anti-emetics.
Kathleen I just read that the trial was officially meant to end in June 2016, if it stops now, that means it didnt even get half way.
-
If the bottles had different pills - don't you think they would instruct us on which bottle to start with. Or at least have a different journal for each bottle. Just my thoughts.
Karyn
-
hmm...makes me wonder. My onc was SUPER specific to tell me to start the new bottle of pills from my last visit and not use any more from the old bottle and to bring that old bottle back next visit. In retrospect, the pills are all the same mg, so maybe they are all the same thing. I agree with Karyn...they would probably be really clear about journaling the differences in side effects in bottles.
-
I think I brought up the bottles and the new SE's. The hint came from my GE doc's p.a. who was mystified by the intensity of my D, even though antibiotics sometimes cause it. I'd taken a lot of Keflex before with no problems. I had just had a check-in visit and had been given new bottles.
I had to take all my pills in for my visits, and always got two new bottles back. I assume they were identical to each other. But they may have been different from the prior quarter's two bottles. The p.a. said that in a double blind, no one knows what they are getting or when they are getting it, and sometimes the study is designed to evaluate tolerances as well as effectiveness. I have no idea if the hypothesis has merit or not.
I didn't realize tht this was due to run until 2016. Wow.
Heather, that was my experience also, except I didn't have D. My neuropathy is improved just over the last few weeks since finishing up, if that helps. Mine was tolerable, though I recommend UGGS for evey occasion
.
Warmly,
Cathy
Cathy
-
HI Ladies,
Okay, I have read here that the study is closed and they are not taking any new participants.
Back in May, I inquired about this study, and had all the paperwork and contact info, but didn't pursue until last week. I emailed the person and she said that the trial was still open.
Then, the next day, they called me for an appointment next Monday to meet with the Dr. who is running this trial. So, it will be interesting to see what happens at that appointment. I will post back.
V
-
May be the trial is closed at certain locations. About the bottles and SE - They want to keep track of all extra meds and that is why they take them back - Some of us take 6,5,4 or less but the bottles all have the same number of pills in them. I get three bottles at each visit and take 5 per day. I guess we all will find out at some point in the future.
Karyn
-
Stupid question... but why do you need a double blind half drug/half placebo?? I mean, if you aren't in the trial, you aren't taking the drug... so couldn't everyone IN the trial get the drug and be compared to those NOT in the trial. Silly, I know... our follow up is different and more detailed... I'm just upset because I am 93% sure I have the placebo!!
-
leanna9 - good point - I think it is a way to compare side effects without being biased. Also there is the "placebo effect" where some people will have an improvement in symptoms bc they "think" they are taking the medication. That may not be the case with this trial. Hang in there, I don't know if this would ever happen, but I think that if a drug showed a significant benefit, they should offer it to those on the placebo. Like others have said, not everyone gets the big D, but I'm not sure if anyone has confirmed they got the drug without the D.
Has anyone who has finished been told whether they were on the drug or not yet?
K
-
I dont think they can tell anyone until the study is "unblinded" for everyone. You are right about the placebo effect....I have a friend who is a trial reseacher for big pharma and they have to take a 30% placebo effect into account. Thats really fascinating to me. That almost 1/3 of the people can change an outcome with mind over matter....HUGE frontier in mind body medicine I wish could be studied by someone with big dollars.
-
I also have a question for the ladies who have finished the year taking Neratinib ! I know there is a few of you out there previously on this topic, but probably less-likely to be looking at the moment ! " after all the diarrhea, anti-emetics, and the year taking the drug, has every effect associated with having taken neratinib returned to NORMAL now " ??? I would like to know IF, like chemo ! have some side effects stayed with you after the years completion ! Thanks...
-
My neuropathy got worse on the trial and had some foot and joint pain that has not recurred since being done. I do still have a bit of neuropathy but, I think this is permanent from the Taxol. I did NOT have a problem with D. Stools were toward loose a lot of the time. After I stopped (mid Aug) I had constipation and am getting back to pre trial normality. Hot flashes were not consistant I had a couple of months during the trial when they lessened. After I quit the pills I still had them bad and they have gone now and I am now menstrating. I guess time will tell on the hormonal fluctuations.
-
Thank-You leighanmar I so appreciate your quick reply, yeah those dam hot-flashes drive us up the wall ! mine where all but gone 5-ish or so mths ago, but now they have returned, thank-fully, milder never the less, cheers.
-
Hi All,
Just got a phone call from Trial nurse and the study is closed in Seattle as well. Oh well..... part of me really wanted to join and part of me was on the fence. Well, the decision was made for me.
V
-
V It looks like they may be rushing neratinib through for FDA, and I guess, thats a good thing, for the sooner they do, the quicker it will be accessible to all HER2+ battlers with early and later stage BCs, including the correct dosage intake, who knows what damage we are doing to our selves being so over dosed ! I mean the damage undiscovered or unpublished yet, like any drug that is over prescribed, the cause and effect.
Month 3 follow up yesterday, study team agreed to dose reduced me to 5 tabs/ 200mg per day, which for now, I am happy to see how I go. D is increasingly difficult to maintain along with other issues. I have also noticed a skin surface lump that appeared out of no-where a few weeks ago below my surgical line, it appeared pimple like at first, since pimples are my thing lately ! but think its to hard for a pimple, the tightness of my skin from radiotherapy and implants make it difficult to know, mentioned it yesterday, but it went unnoticed in the urgency of the moment, I maybe just a worry wort...
-
Oh wow, where did you hear about the fda rush for approval? Very cool...as I spent all night unable to sleep with a gurgling tummy!
-
Kaka...maybe you need to drop some more. Lots of women are fine at 4 pills and even more telling is that the new trial dosed eveeyone with 3 pills. More than likely we were getting double what we need!
-
yes, true thanks geewhiz, how-ever I did mean that it looks like that is one of the reasons for stopping the trial prematurely, from early results seen, read review somewhere, medscape, pharma-letter, all still speculation I think, and yes I should be sure where I read it before making that statement, sorry I didnt take note because its so many years before we get to where you are, will find out.
-
Oh please post good news away! I am not one who gripes about others posting without knowing the birthdate and blood type of the trial researcher, lol. I have been on the wrong side of that many times myself!
: ) -
whoops, NDA (new drug application) not FDA, chemo-brain strikes again ! Thank you again geewhiz
-
I'm six months in and on 5. I asked this before and no one replied.... Has anyone else lost weight? I lost around 15 lbs as soon as I started - wasn't hungry. I'm worried about finishing and my appetite improving. I lost weight with Herceptin too without trying.
Karyn
-
Wow, must not be on the trial. My appetite is still there. I must be the only one gaining weight on this trial :-) Possibly an indication I'm not on the drug?? I was on Herceptin too, same thing. Had bad acid reflux toward the end, but could eat pretty well otherwise.
-
I have lost my appetite too, and some food taste differant, I have lost weight but gained it back again after forcing myself to double my food intake that is of binding nature, like lots of bananas boiled-rice, boiled-eggs with added anti-emetics worked for me, but having problems getting my WCC up again, bloods still say I have mild neutropenia... I hate the fact that my immune system is so vulnerable in picking up an infection, virus, or anything blowing my way ! Herceptin for the most part WCC was ok, I was on neulasta with chemo and wonder if my immune-system/bone marrow is imparted now, or does neratinib slowly cause white-cell depletion ? any thoughts on that one...
-
gemini - I wouldn't interpret appetite as a sign... Just one thing I noticed. I seemed to have plateau'd out and my weight is stable now. I also had other things going on in my life which may have effected the weight... I got divorced during chemo (found out my husband was having an affair), my dad died during chemo, and I've dated and broken up with others since starting the trial.
-
I lost weight the first 3 months because I felt nauseated if I ate more than a few bites at a time. I gained it back the next 9 months.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team