access-principles-1access-principles-2access-principles-3backcarrierdevelopmentease_of_administrationexportimplantableinjectablenon-implantablenon_carriernon_injectableother_featuresprintroute_of_administrationtherapeutic_areatype_of_tech

Type of technology

Intra-vaginal ring

Administration route

Topical (Vaginal)

Development state and regulatory approval

Active Pharmaceutical Ingredient (API)

Dapivirine (DPV)

Development Stage

Marketed

Regulatory Approval

Positive scientific opinion from the European Medicines Agency for use among women ages 18 and older in developing countries. in WHO guidelines

Description

Silicone matrix vaginal ring delivering dapivirine over one month.

Developer(s)

International Partnership for Microbicides
United States

IPM's mission is to develop HIV prevention products and other sexual and reproductive health technologies for women, and to make them available and accessible where they are urgently needed.

Population Council
Global

The Population Council is a leading research organization dedicated to building an equitable and sustainable world that enhances the health and well-being of current and future generations. We generate ideas, produce evidence, and design solutions to improve the lives of underserved populations around the world.

Technology highlight

The ring is made of a flexible silicone polymer and contains the ARV dapivirine, an NNRTI, which is dispersed in the silicone matrix and slowly released over the course of a month. The ring delivers dapivirine directly at the site of potential HIV infection, with low systemic absorption. Women insert the flexible, long-acting ring themselves into the vagina and replace it every month.

Illustration(s)

Technology main components

dapivirine and silicone

Information on the raw materials sourcing, availability and anticipated price

9 to 13 USD/ring

Delivery device(s)

Silicone vaginal ring

APIs compatibility profile

API desired features
Small molecules

dapivirine

Additional solubility data

Not provided

Additional stability data

Not provided

API loading: Maximum drug quantity to be loaded

< 10 wt%

API co-administration

1 single API : Still being investigated

LogP

Not provided

Scale-up and manufacturing prospects

Scale-up prospects

current scale: ~9000 rings future scale (2022 and beyond): ~45000 rings

Tentative equipment list for manufacturing

injection molding machine mixer automated inspection machine automated packaging machine

Manufacturing

GMP ISO class 8 area

Specific analytical instrument required for characterization of formulation

HPLC tensile tester dissolution apparatus analytical balance

Excipients

Proprietary excipients used

silicone elastomer for extended use

Novel excipients or existing excipients at a concentration above Inactive Ingredient Database (IID) for the specified route of administration

excipient has been included in regulatory dossier for product

Residual solvents used

No residual solvent used

Additional features

Other features of the technology
  • Drug-eluting
  • Removable
  • Molded
  • Room temperature storage
  • At least 1 year shelf life
Release properties

Releases dapivirine over a one-month period

Injectability

Not Applicable

Safety

There were no safety concerns with long-term use of the ring in Phase III clinical studies. Data from two open-label (Phase IIIB) studies show a similar favorable safety profile as do 12 smaller safety studies.

Stability

ICH Climate Zone IV (A/B)

Storage conditions and cold-chain related features

5 years shelf life This product does not require specific temperature storage conditions. Store in the original package to protect from light.

Therapeutic area(s)

  • HIV
Use case(s)
  • Pre-Exposure Prophylaxis (PrEP)

Potential associated API(s)

Use of technology

Ease of administration
  • Administered by a community health worker
  • Administered by a nurse
  • Administered by a specialty health worker
  • Self-administered
Frequency of administration

Monthly

User acceptance

Phase III and open label extension studies indicate a high user acceptance

Targeted user groups

Age Cohort
  • Adolescents
  • Adults
Genders
  • Female
Pregnant individuals

Yes

Lactating individuals

Yes

Healthy individuals

Yes

Comment

Women at substantial risk of contracting HIV through receptive vaginal sex

Class(es)

microbicide

Development stage

Marketed

Clinical trial number(s)

Not provided

Foreseen/approved indication(s)

Prevention of HIV infection through vaginal sex

Foreseen user group

women older than 18 at substantial risk of contracting HIV through vaginal sex

Foreseen duration between application(s)

1 month

Applications to Stringent Regulatory Authorities (SRA) / regulatory approvals

Positive scientific opinion from the European Medicines Agency for use among women ages 18 and older in developing countries. in WHO guidelines

Publications

Evaluating the potential impact and cost-effectiveness of dapivirine vaginal ring pre-exposure prophylaxis for HIV prevention. 
Reidy M, Gardiner E, Pretorius C, Glaubius R, Torjesen K, Kripke K. 
PLoS One. 2019;14(6):e0218710. 
Published 2019 Jun 26. doi:10.1371/journal.pone.0218710

Background
Expanded HIV prevention options are needed to increase uptake of HIV prevention among women, especially in generalized epidemics. As the dapivirine vaginal ring moves forward through regulatory review and open-label extension studies, the potential public health impact and cost-effectiveness of this new prevention method are not fully known. We used mathematical modeling to explore the impact and cost-effectiveness of the ring in different implementation scenarios alongside scale-up of other HIV prevention interventions. Given the knowledge gaps about key factors influencing the ring’s implementation, including potential uptake and delivery costs, we engaged in a stakeholder consultation process to elicit plausible parameter ranges and explored scenarios to identify the possible range of impact, cost, and cost-effectiveness.

Methods and findings
We used the Goals model to simulate scenarios of oral and ring pre-exposure prophylaxis (PrEP) implementation among female sex workers and among other women ≤21 years or >21 years with multiple male partners, in Kenya, South Africa, Uganda, and Zimbabwe. In these scenarios, we varied antiretroviral therapy (ART) coverage, dapivirine ring coverage and ring effectiveness (encompassing efficacy and adherence) by risk group. Following discussions with stakeholders, the maximum level of PrEP coverage (oral and/or ring) considered in each country was equal to modern contraception use minus condom use in the two age groups.

We assessed results for 18 years, from 2018 to 2035. In South Africa, for example, the HIV infections averted by PrEP (ring plus oral PrEP) ranged from 310,000 under the highest-impact scenario (including ART held constant at 2017 levels, high ring coverage, and 85% ring effectiveness) to 55,000 under the lowest-impact scenario (including ART reaching the UNAIDS 90-90-90 targets by 2020, low ring coverage, and 30% ring effectiveness). This represented a range of 6.4% to 2.2% of new HIV infections averted. Given our assumptions, the addition of the ring results in 11% to 132% more impact than oral PrEP alone. The cost per HIV infection averted for the ring ranged from US$13,000 to US$121,000.

Conclusions
This analysis offers a wide range of scenarios given the considerable uncertainty over ring uptake, consistency of use, and effectiveness, as well as HIV testing, prevention, and treatment use over the next two decades. This could help inform donors and implementers as they decide where to allocate resources in order to maximize the impact of the dapivirine ring in light of funding and implementation constraints. Better understanding of the cost and potential uptake of the intervention would improve our ability to estimate its cost-effectiveness and assess where it can have the most impact.

Safety , adherence , and HIV-1 seroconversion among women using the dapivirine vaginal ring ( DREAM ): an open-label , extension study. 
Nel A, Niekerk N Van, Baelen B Van, et al. 
Lancet HIV. 2021;8:77-86. doi:10.1016/S2352-3018(20)30300-3

Background
The Ring Study, a phase 3 trial in 1959 sexually active women (randomised 2:1), showed a favourable safety profile and a 31% HIV-1 infection risk reduction for a vaginal ring containing 25 mg of dapivirine, compared with a placebo ring. We report here the DREAM study, which aimed to evaluate safety, adherence, and HIV-1 incidence in those using the dapivirine vaginal ring (DVR) in open-label use.

Methods
The DREAM study is an open-label extension of The Ring Study, done at five research centres in South Africa and one research centre in Uganda. Former participants from The Ring Study, who remained HIV-negative and who did not discontinue the study due to an adverse event or safety concern that was considered to be related to the investigational product, were eligible. Women who were pregnant, planning to become pregnant, or breastfeeding at screening for DREAM were excluded. All participants received the DVR for insertion at the enrolment visit. Participants attended a 1-month follow-up visit and could either proceed with visits once every 3 months or attend monthly visits up to month 3 and then continue with visits once every 3 months. At each visit, HIV testing and safety evaluations were done, and residual dapivirine measured in used rings (approximately 4 mg is released from the DVR over 28 days of consistent use). HIV-1 incidence was compared descriptively with the simulated incidence rate obtained from bootstrap sampling of participants in the placebo group of The Ring Study, matched for research centre, age, and presence of sexually transmitted infections at enrolment. This study is registered with ClinicalTrials.gov, NCT02862171.

Findings
Between July 12, 2016, and Jan 11, 2019, 1034 former participants from The Ring Study were screened, 941 were enrolled and 848 completed the trial. 616 (65·5%) of 941 participants reported treatment-emergent adverse events. Of these, six (0·6%) had events considered to be treatment-related. No treatment-related serious adverse events were reported. Measurements of monthly ring residual amounts in participants enrolled in both trials showed consistently lower mean values in DREAM than in The Ring Study. Arithmetic mean ring residual amounts of participants in The Ring Study DVR group who enrolled in DREAM were 0·25 mg lower (95% CI 0·03–0·47; p=0·027) than the mean ring residual amounts of these participants in The Ring Study. 18 (1·9%) HIV-1 infections were confirmed during DVR use, resulting in an incidence of 1·8 (95% CI 1·1–2·6) per 100 person-years, 62% lower than the simulated placebo rate.

Interpretation
Although efficacy estimation is limited by the absence of a placebo group, the observed low HIV-1 incidence and improved adherence observed in DREAM support the hypothesis that increased efficacy due to improved adherence occurs when women know the demonstrated safety and efficacy of the DVR. The feasibility of a visit schedule of once every 3 months was shown, indicating that the DVR can be used in a real-world situation in usual clinical practice.

Collaborate for development

Consider on a case by case basis, collaborating on developing long acting products with potential significant public health impact, especially for low- and middle-income countries (LMICs), utilising the referred to long-acting technology

Share technical information for match-making assessment

Provide necessary technical information to a potential partner, under confidentiality agreement, to enable preliminary assessment of whether specific medicines of public health importance in LMICs might be compatible with the referred to long-acting technology to achieve a public health benefit

Work with MPP to expand access in LMICs

In the event that a product using the referred to long-acting technology is successfully developed, the technology IP holder(s) will work with the Medicines Patent Pool towards putting in place the most appropriate strategy for timely and affordable access in low and middle-income countries, including through licensing