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"On-demand" HIV prevention method for women b

<p>A fast-dissolving vaginal insert that women would use at or around the time of sex as an &ldquo;on-demand&rdquo; HIV prevention method is being evaluated in a new early phase study being conducted by <a href="https://www.matrix4prevention.org/">MATRIX</a>, a United States Agency for International Development (USAID)-funded project focused on the early research and development of innovative HIV prevention products for women.&nbsp; The MATRIX study is only the second Phase 1 trial of the <a href="https://www.matrix4prevention.org/products/tafevg-fast-dissolving-vaginal-insert">fast-dissolving insert</a> used vaginally and the first to evaluate its use in African women. The insert, which contains the antiretroviral (ARV) drugs tenofovir alafenamide (TAF) and elvitegravir (EVG), is the only on-demand HIV prevention product for use by women currently being evaluated in clinical trials.</p>

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New early phase study evaluates "on-demand" HIV prevention method for women

A fast-dissolving vaginal insert that women would use at or around the time of sex as an "on-demand" HIV prevention method is being evaluated in a new early phase study being conducted by MATRIX, a United States Agency for International Development (USAID)-funded project focused on the early research and development of innovative HIV prevention products for women.

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Slow dissolving, longer-acting HIV prevention method in the pipeline

Research launched to determine ring’s practicability and acceptability ahead of first-in-human study of monthly dapivirine film.

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AIM ImmunoTech Announces Encouraging Translational Data from Phase 2 Study Evaluating Ampligen® for the Treatment of Advanced Recurrent Ovarian Cancer

AIM ImmunoTech Announces Encouraging Translational Data from Phase 2 Study Evaluating Ampligen® for the Treatment of Advanced Recurrent Ovarian Cancer
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Study launched to test a vaginal film that slowly dissolves over the course of 30 days

A vaginal film designed to slowly dissolve over the course of 30 days is being put to the test for the first time in a study launched this week that aims to determine its feasibility and acceptability as a potential HIV prevention method for women.

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