You are now leaving XTANDI.com
The website you are about to visit is not owned or controlled by Astellas. Astellas are not responsible for the information or services on this site.
“Astellas has invested more than a decade and more than $1.4 billion to research and develop XTANDI and successfully bring this innovative cancer treatment to market for patients with advanced prostate cancer. XTANDI is priced in line with other oral therapies for advanced prostate cancer available in the U.S. today and is widely available for patients across the health insurance marketplace. Based on an analysis of third-party claims data, 70% of US patients paid less than $100 in out-of-pocket costs for their XTANDI prescription in 2021 regardless of insurance type.”
- Company Spokesperson, Astellas Pharma U.S., Inc.
Astellas has invested more than a decade and more than $1.4 billion to research and develop XTANDI (enzalutamide) and successfully bring this innovative cancer treatment to market for patients with advanced prostate cancer. At Astellas, we believe the price of medicines should reflect the value they bring to patients, healthcare systems, and society. Astellas is dedicated to working with policymakers and stakeholders across the healthcare system to find solutions that balance the need to foster medical innovation and ensure affordable access to medicines for patients.
XTANDI is widely available among U.S. patients and is the most prescribed branded drug for those living with advanced prostate cancer. XTANDI is the first and only novel hormone therapy (NHT) approved by the U.S. Food and Drug Administration (FDA) in three types of advanced prostate cancer: non-metastatic castration-resistant prostate cancer (nmCRPC), metastatic castration-resistant prostate cancer (mCRPC) and metastatic castration-sensitive prostate cancer (mCSPC). In all three types for which it is approved, data have shown that XTANDI helped slow advanced prostate cancer progression, demonstrating a significant reduction in the risk of disease progression or death.
The Bayh-Dole Act – enacted in 1980 – incentivizes public-private collaborations that expand consumer access to new and potentially groundbreaking products and supports America’s global leadership in medical innovation and biopharmaceutical manufacturing. The National Institutes of Health (NIH) has consistently held the position that invoking the Bayh-Dole Act’s “march-in” rights authority is not an appropriate means to control prescription drug prices.
XTANDI is a prime example of how collaboration between early-stage public research and private development can benefit American consumers, as the Bayh-Dole Act envisioned.
In 2016, the NIH concluded that XTANDI is broadly available as a prescription drug and declined to exercise its “march-in” rights under the Bayh-Dole Act.
Invoking “march-in” rights as a means of controlling prescription drug prices could undercut the purpose of the Bayh-Dole Act to encourage the commercialization of Subject Inventions and could discourage the development of future innovations and medical breakthroughs by deterring future public-private collaborations.
While the U.S. government contributed approximately $500,000 to the initial discovery of the molecule that eventually became XTANDI, Astellas and its partners have invested more than $2.2 billion to support the extensive clinical trials and research necessary to demonstrate that XTANDI is safe and effective for patients, support the application that led to FDA approval, and further understand which patients will benefit from treatment. Astellas alone has invested more than $1.4 billion to date in research and development efforts for XTANDI.
Astellas is dedicated to improving access and affordability for patients who rely on our medications and working collaboratively with stakeholders across the healthcare system to find avenues that meet the dual imperatives of encouraging drug development and innovation while ensuring access to and affordability of medicines.
XTANDI is priced in line with other oral therapies for advanced prostate cancer available in the U.S. today. Recent references to the average wholesale price (AWP) of XTANDI are misleading reflections of what most purchasers and patients actually pay for XTANDI. It is important to note that a drug’s list price does not account for rebates that manufacturers individually negotiate with insurance companies, and the AWP does not reflect the amount most patients will pay for their prescription medications at the pharmacy counter. The facts demonstrate what patients actually pay. For instance, based on an analysis of third-party claims data:
On the whole, the average out-of-pocket cost a patient with commercial insurance or Medicare Part D would pay for XTANDI is $254.88 or $226.40 per month, respectively.
Additionally, active-duty TRICARE patients have a $0 co-pay for XTANDI, and non-active-duty TRICARE patients can access XTANDI by mail-order supply, in the retail setting or a military treatment facility for co-pays ranging from $0 to $14.
Astellas offers assistance to patients through XTANDI Support Solutions, such as information about healthcare coverage options and financial assistance options – including co-pay assistance to eligible commercially insured patients. Astellas also provides XTANDI at no cost to eligible patients who do not have insurance or who are underinsured through the Astellas Patient Assistance Program.
However, Astellas recognizes that such patient assistance programs are not a long-term solution to outdated benefit designs that create access and affordability challenges for the patients we serve and others. Astellas is committed to working with policymakers and stakeholders across the healthcare system to find durable policy solutions that ensure patients can afford and access the medicines they need, while preserving an environment that enables U.S. biopharmaceutical companies to continue to invest in innovative research on behalf of patients.
* Source: Symphony Health, IDV®, January 1, 2021 – December 31, 2021.
This website is intended for U.S. residents only. This website contains information about products that may not be available in all countries, or may be available under different trademarks, for different indications, or in different dosages. Nothing contained herein should be considered a solicitation, promotion or advertisement for any drug including those under development. Any information on the products contained herein is not intended to provide medical advice nor should be used as a substitute for the advice provided by your physician or other healthcare provider.