The only recent coverage I’ve seen so far about the FDA’s relabeling of tamoxifen on is from the PGx Reporter, which is subscription-only. Here’s their public excerpt:
FDA Panel Leans Toward Including CYP2D6 Dx in Tamoxifen Label, But is Split on Language
The Pharmaceutical Science Clinical Pharmacology Subcommittee was split over whether the label should “recommend” the genetic test or make it an “option” for health care providers and patients to discuss.
As it considers just how strong the wording on the label should be, the FDA is looking at the role of endoxifen (the active metabolite), 2D6, and drug interactions.
The only recent coverage I’ve seen so far about the FDA’s relabeling of tamoxifen on is from the PGx Reporter, which is subscription-only. Here’s their public excerpt:
As it considers just how strong the wording on the label should be, the FDA is looking at the role of endoxifen (the active metabolite), 2D6, and drug interactions.
We’re getting many inquiries ourselves into the Tamoxifen 2D6 Test. Here are recently asked questions and answers, and previous posts on Tamoxifen and 2D6 Testing.
This entry was posted on Thursday, November 16th, 2006 at 12:52 pm and is filed under Breast Cancer, Drug Response, Genetic Testing, Privacy, Legislation & Policy. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your own site.