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  • HIV Experts Propose New Pathway for Conducting Phase 3 Drug Trials

    We face a new scientific challenge: how to demonstrate the safety and efficacy of promising new antiretroviral drugs when the two traditional study designs – the superiority trial and the non-inferiority trial – are no longer useful in showing improvements in both “treatment experienced” patients and those who have never received drug therapy (treatment-naïve patients).

    07 February 2012 | Forum for Collaborative HIV Research
  • New Gilead GS 7340-Inclusive Fixed-Dose Combo Tablet Trial Announced

    Gilead Sciences Inc. (Nasdaq: GILD) today announced the start of a Phase II clinical trial to evaluate a modified version of its experimental “quad” fixed-dose combination (FDC) tablet currently being reviewed by the U.S. Food and Drug Administration, according to a company announcement.

    30 January 2012 | AIDSMeds
  • Gilead Initiates Phase 2 Clinical Trial Evaluating GS-7340, A Low-Dose Novel Prodrug of Tenofovir

    The Phase 2 study will evaluate GS-7340 as part of a once-daily, co-formulated single-tablet regimen that will also contain the boosting agent cobicistat, the integrase inhibitor elvitegravir, and Emtriva(R) (emtricitabine). The GS-7340-containing single-tablet regimen will be compared to Gilead's Quad single-tablet regimen, which contains Viread and Emtriva (as Truvada(R)), elvitegravir and cobicistat, and is currently under review for marketing approval by U.S. and European regulatory agencies.

    24 January 2012 | Gilead press release
  • Pathogenic Landscape of HIV

    In perhaps the most comprehensive survey of the inner workings of HIV, an international team of scientists led by researchers at the University of California, San Francisco has mapped every apparent physical interaction the virus makes with components of the human cells it infects—work that may reveal new ways to design future HIV/AIDS drugs.

    21 December 2011 | UCSF Today
  • Gilead Files European Marketing Application for the Quad, a Once-Daily Single-Tablet Regimen for the Treatment of HIV Infection

    Gilead Sciences, Inc. (Nasdaq:GILD) announced today that the Marketing Authorisation Application (MAA) for the Quad single-tablet regimen of elvitegravir, cobicistat, emtricitabine and tenofovir disoproxil fumarate for the treatment of HIV-1 infection in adults, submitted on November 24, 2011, has been validated by the European Medicines Agency (EMA).

    21 December 2011 | Gilead press release
  • Gilead's New HIV Drug Pipeline: What You Need To Know For 2012

    Gilead Sciences (GILD) has a current portfolio dominated by HIV treatment drugs. More than 70% of its sales come from HIV treatment products. However it also discovers, develops, and commercializes treatments for other infectious and pulmonary diseases.

    20 December 2011 | Seeking Alpha
  • Testing nasal vaccine for HIV treatment

    Researchers are working to find out whether a HIV vaccine developed by a Norwegian biotech company can be administered nasally.

    19 December 2011 | Health Canal
  • Novel HIV-Associated Diarrhea Drug Crofelemer Goes to FDA for Approval Review

    Raleigh, North Carolina-based Salix Pharmaceuticals announced on Tuesday, December 14, that it has submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) requesting approved for Crofelemer, a novel therapy for HIV-associated diarrhea. 

    15 December 2011 | AIDSMeds.com
  • Aethlon Medical Announces HIV-AIDS Research Discovery

    Aethlon Medical, the pioneer in developing therapeutic filtration devices to address infectious disease and cancer, announced today that researchers have discovered that the Aethlon Hemopurifier® is able to capture particles known as Nef protein exosomes, which contribute to the progression of human immunodeficiency virus (HIV) infection to acquired immunodeficiency syndrome (AIDS).

    15 December 2011 | PR Newswire (press release)
  • Gilead Announces Two-Year Data From Pivotal Phase 3 Study of Elvitegravir

    Company to Submit U.S. Regulatory Filing for Elvitegravir in Second Quarter of 2012

    09 December 2011 | Market Watch
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