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In March 2017, the WHO reclassified progestogen-only injectable contraceptives including DMPA (also known as Depo) and NET-EN as MEC 2, the classification for methods for which the benefits outweigh the theoretical risks, emphasizing that women had a right to know about all of the risks and benefits associated with a method. This step reflected ongoing concern about the possibility that injectable progestogen-contraceptives increase women’s risk of acquiring HIV. There are mixed data from observational studies, primarily focused on DMPA, with far less known about NET-EN or about the subcutaneous formulation of DMPA, branded as Sayana Press. An ongoing randomized controlled trial known as ECHO, scheduled to release data in 2019, is evaluating whether DMPA injections, the copper IUD and the contraceptive implant impact women’s HIV risk. This session will provide updates on the array of moving pieces, including the research, programmatic and advocacy components, and their implications.

10:15
Welcome and Introduction to the session
Mitchell Warren, AVAC, United States
Beth Schlachter, United States
10:20
Planning ahead for Family Planning 2020
Beth Schlachter, United States
10:35
Medical Eligibility Criteria for injectable contraceptives
Petrus Steyn, Human Reproduction Team, WHO Department of Reproductive Health and Research, Switzerland
10:50
ECHO trial update
Helen Rees, South Africa
11:05
Civil society engagement
Yvette Raphael, APHA, South Africa
11:20
Panel discussion
11:20
Panel discussion
Emily Bass, AVAC, United States
Petrus Steyn, Human Reproduction Team, WHO Department of Reproductive Health and Research, Switzerland
Helen Rees, South Africa
Yvette Raphael, APHA, South Africa
Lillian Mworeko, International Community of women living with HIV Eastern Africa (ICWEA), Uganda
Heather Watts, Office of the Global AIDS Coordinator, US Department of State, United States
12:00
Now what?
Mitchell Warren, AVAC, United States
Beth Schlachter, United States