Info for Lucanix compassionate use - 1251505

meanie11
Posts:12

I am looking for any information on how to request for compassionate use of lucanix from NovaRx. My mom is running out of treatment options and feel Lucanix may help her. Does anyone have any information as to the contact person and procedure in applying for compassionate use of lucanix? How long does this application/approval process take? I heard NovaRx is generous with allowing lucanix compassionate use. Anyone currently taking Lucanix via compassionate use? Thank you. Any information is greatly appreciated.

Forums

certain spring
Posts: 762

I'm sorry to hear about your mother. While you're waiting for a doctor to answer, I thought it might be helpful to link to a post Dr West wrote about compassionate use programmes:
http://cancergrace.org/cancer-101/2010/12/18/compassionate-use/
and a research briefing from Dr Govindan that covers Lucanix:
http://cancergrace.org/lung/files/2012/06/Govindan-Immunotherapies-for-…
There was a discussion on Inspire about eligibility which you've probably seen, dating back to the summer of 2012:
http://www.inspire.com/groups/lung-cancer-survivors/discussion/lucanix-…
The questions raised there were whether the company required a patient to have stable disease, and whether they were still running a compassionate use program at all. Hopefully someone here will have more recent information on these points. All best.

catdander
Posts:

meanie, I think certain spring has given you about as much information as we have unless I was to just get lucky in the choosing a doctor who happened to know someone who was giving lucanix on a compassionate use program. I think contacting Lucanix directly may give you the best current information available. http://www.lucanix.org/aboutlucanix.shtml

Please let us know what you find.

Janine

Dr West
Posts: 4735

I don't have any additional information about Lucanix, but I just wanted to inject my view of why the Lucanix compassionate use program hasn't been a priority for me. Lucanix has been the subject of optimism that I fear may not be met by actual results, which is what we saw with Stimuvax. I feel that the negative trial results from Stimuvax should provide a reminder that we would be mistaken in presuming that these unproven therapies will be valuable. I don't see that as a problem when the most appropriate alternative is no active treatment, but I don't personally favor a strategy that defers treatments that have a proven value in favor of a therapy that does not and isn't answering a clinical research question that will move the field forward.

-Dr. West

kate0228
Posts: 36

I have a question about the Lucanix trial. I was reading about it and noticed that if a person had a splenectomy, that would exclude them from the trial. Just curious, only because if this drug is ever approved, I would assume Tony couldn't take the drug due to having his spleen out in 1993? Back then, it was standard procedure to remove it. For a guy without his spleen, I am always amazed at how he never gets sick (other than lung cancer, haha) - meaning colds & flu. His blood counts consistently hang in there on all the different chemos thrown at him - except Taxotere. They dropped on that but he rebounded very quickly. Is it unusual that he has a very strong immune system even without a spleen?

Dr West
Posts: 4735

I don't have enough of an expertise in immunology to say how much of an effect a splenectomy really has, but I think it's understandable that treatment with an immunotherapy wouldn't be presumed to be as likely to work in someone with a splenectomy. I don't think that means it couldn't work, but rather that you might want to ensure that the people in the trial testing the efficacy of a new immune-based treatment would have the best chance of benefiting from it.

-Dr. West