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April 4, 2022

ABC Statement: On the FDA’s Blood Donor Deferral Policy for Men Who Have Sex with Other Men (MSM) & the ADVANCE Study

By America's Blood Centers

America’s Blood Centers (ABC) reiterated its call for a safe and available blood supply that that treats all potential donors with fairness, equality, and respect in a statement addressing the U.S. Food and Drug Administration’s (FDA) blood donation eligibility criteria for gay and bisexual men. ABC supported the FDA policy change in 2020 that reduced the donor deferral period from 12 to three months for men who have sex with other men (MSM). Important work is now occurring to collect the needed scientific evidence to further evaluate the current blood donation policy for gay and bisexual men. ABC strongly supports this effort as a pathway to the establishment of donor-screening based on individual risk behaviors, not sexual or gender identity.

The ADVANCE study is a pilot study funded by the FDA that focuses on the blood donor deferral policy for MSM. Three blood collection organizations, including ABC-member’s OneBlood and Vitalant, are currently collaborating with LGBTQ community centers and organizations in eight locations to enroll participants. The study seeks to determine if different eligibility criteria can be used at blood centers nationwide that focuses on each donor’s individual risk behavior rather than their sexual orientation.

The FDA initially instituted a lifetime deferral on blood donations for MSM in 1983 to reduce the chance of HIV in the blood supply at a time when testing was limited or non-existent. In 2015, the FDA revised this policy and moved to a 12-month deferral in response to comprehensive testing and data demonstrating safety in shortened deferral. This policy was revised again in 2020 to the current 3-month deferral during the COVID-19 public health emergency.

Gay and bisexual men are being enrolled in the ADVANCE study to collect data on the performance in assessing risk of new questions that may be added to the donor history questionnaire in the future. The results, which are expected in late 2022, will be submitted to the FDA for review and the agency will then decide the next steps in this process, including how the data will be released to the public.

Download the full statement.

Posted in Advocacy, News, Statements
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