The Methods for Improving Reproductive Health in Africa (MIRA) Study SOC PROGRAM

1. The Methods for Improving Reproductive Health in Africa (MIRA) Study SOC PROGRAM Liz Montgomery Women’s Global Health Imperative RTI International GCM SOC Consultation June 19, 2008

2. Partners • Women’s Global Health Imperative: University of California San Francisco • Ibis Reproductive Health, USA & RSA • University of Zimbabwe-UCSF Collaborative Research Programme, Zimbabwe • Medical Research Council, Durban RSA • Perinatal HIV Research Unit, Johannesburg, RSA • Funder: Bill & Melinda Gates Foundation

3. Study Aims To examine the effectiveness of the diaphragm and lubricant gel for preventing HIV acquisition in women • Primary endpoint: HIV acquisition • Secondary endpoints: cervical STIs (GC & CT)

4. Study Design All women received risk reduction counseling, free male condoms and diagnosis and treatment of curable STIs

5. Total n = 5045 UZ-UCSF Harare, Zimbabwe n=2502 PHRU Soweto, South Africa n=1028 MRC Durban, South Africa n=1515 MIRA Trial Sites

6. Zimbabwe Standard of Care at start of MIRA trial • ARV’s available only as part of research studies. These are few and small, but UZ-UCSF has direct relationships with the investigators of these studies. • MOH planned to roll out nationwide generic ART programme at tertiary hospitals, but unknown exactly when this would happen

7. MIRA: Current Standard of Care • Screened HIV+ MIRA women: • Professional pre and post-test counseling for woman and partner • STI screening and treatment for woman and partner • 2-week follow-up supportive counseling visit at MIRA • Referral to social services, support groups and “moving-on” clubs, HIV care organizations • Referral to research studies providing ART (DART, Duke) and studies specializing in discordant couples (HPTN 052)

8. MIRA: Current Standard of Care • Seroconverters: • Same as screened HIV+ women, except that seroconverters stay in study, therefore have ongoing access to clinical care for themselves and partners. This includes pregnancy and STI screening and treatment for any medical problems.

9. Standard of Care • “Moving target” - National ARV programmes and “standard of care” for research studies evolving as study progressed; • Gates Foundation aware that what they approved for MIRA would set a precedent • Equity, sustainability huge concerns

10. MIRA SOC program - theory • (Official) Overall goal was to transition all MIRA seroconverters into the National ARV Programme in Zimbabwe or South Africa before the end of the trial period (thereby ensuring sustainability) • Explicitly, we did not plan to assume responsibility for care and treatment

11. Timeline 2003 2004 2005 2006 2008 2007 MIRA ended MIRA initiated MIRA SOC initiated SOC IE interviews

12. MIRA SOC – Operationalization • Durban: MOUs with organizations, clinics and hospitals • Soweto: Referral to co-located facility with psychosocial support and ART • Harare: Referral to local psychosocial support and OI clinics (in theory) • At all sites: referral to ART studies viewed as equivalent to National Tx Programmes

13. Zimbabwe in reality • Social welfare> OI clinic/ CD4 testing> ART • CD4 testing done by trial, trial paid for small subsidy for cost of ART if needed, during study • Paper at social welfare • National shortages/ slots ran out • Connections

14. MIRA Standard of Care Program Results

15. Summary of linkage success • Harare: 74% • Durban: 37% • Soweto: 69% • 13 of 300+ accessing ARVs

16. SOC Challenges • Country-level: National programmes are new and face challenges of their own – staff shortages, ARV shortages (Zim); • Study-level: Difficult for research study team to manage a “care” package in a variety of different settings, with varying resources, different relationships with local organizations, and different resources • Participant-level: Some participants difficult to reach, in denial about serostatus/ need for ARVs, some already passed away by the time SOC implemented

17. Key unanswered questions • Why such low uptake • Where are they now?