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Gilead Sciences Announces Second Quarter 2025 Financial Results

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) announced today its second quarter 2025 results of operations. “This was a very successful second quarter for Gilead, including the FDA approval for Yeztugo as the world’s first twice-yearly HIV prevention option,” said Daniel O’Day, Gilead’s Chairman and Chief Executive Officer. “Our strong growth this quarter was driven by Biktarvy, Descovy, Trodelvy and Livdelzi, reflecting the diversity of our portfolio. As we enter...
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Vir Biotechnology Provides Corporate Update and Reports Second Quarter 2025 Financial Results

SAN FRANCISCO--(BUSINESS WIRE)--Vir Biotechnology, Inc. (Nasdaq: VIR), today provided a corporate update and reported financial results for the second quarter ended June 30, 2025. “We achieved several important milestones across our pipeline, reflecting our commitment to our mission of powering the immune system to transform lives,” said Marianne De Backer, Chief Executive Officer, Vir Biotechnology. “The initiation of our Phase 1 study of PRO-XTEN™ dual-masked VIR-5525 positions us to potentia...
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Human Immunodeficiency Virus (HIV) Rapid Test Kits Strategic Analysis Report 2024-2030 | Expansion of Government and NGO Screening Programs Accelerates Demand in Low-Resource and High-Burden Regions - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Human Immunodeficiency Virus (HIV) Rapid Test Kits - Global Strategic Business Report" report has been added to ResearchAndMarkets.com's offering. The global market for Human Immunodeficiency Virus (HIV) Rapid Test Kits was estimated at US$814.3 Million in 2024 and is projected to reach US$1.2 Billion by 2030, growing at a CAGR of 6.2% from 2024 to 2030. This comprehensive report provides an in-depth analysis of market trends, drivers, and forecasts, helping you ma...
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Soleo Health Achieves ACHC Accreditation for Four Services

FRISCO, Texas--(BUSINESS WIRE)--SOLEO HEALTH ACHIEVES ACHC ACCREDITATION FOR FOUR SERVICES...
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Gilead Receives Positive CHMP Opinions Under Accelerated Review From European Medicines Agency for Twice-Yearly Lenacapavir for HIV Prevention

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion under accelerated review recommending lenacapavir—the company’s injectable HIV-1 capsid inhibitor—for use as pre-exposure prophylaxis (PrEP) to reduce the risk of sexually acquired HIV-1 in adults and adolescents with increased HIV-1 acquisition risk. The final European Commissi...
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Gilead Sciences to Release Second Quarter 2025 Financial Results on Thursday, August 7, 2025

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) announced today that its second quarter 2025 financial results and guidance will be released on Thursday, August 7, 2025 after the market closes. At 4:30 p.m. Eastern Time that day, Gilead’s management will host a webcast to discuss the company’s second quarter 2025 financial results and provide a business update. A live webcast will be available in the Investors section of www.gilead.com and will be archived there for o...
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‘Ohh, Mamma!’ AHF’s Free Sexy Burlesque Encore Revisits LA

LOS ANGELES--(BUSINESS WIRE)--‘Ohh, Mamma!’ AHF’s Free Sexy Burlesque Encore Revisits LA...
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AHF Applauds Congress for Backing PEPFAR Funding in Bipartisan Vote

WASHINGTON--(BUSINESS WIRE)--AHF Applauds Congress for Backing PEPFAR Funding in Bipartisan Vote...
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ViiV Healthcare data show 89% of treatment-naïve people with HIV choose to switch to long-acting injectable Vocabria + Rekambys from daily pills after achieving rapid viral suppression

LONDON--(BUSINESS WIRE)--ViiV Healthcare, the global specialist HIV company majority owned by GSK, with Pfizer and Shionogi as shareholders, today announced data from the phase IIIb VOLITION study demonstrating that 89% (n=129/145) of eligible treatment-naïve people living with HIV opted to switch to long-acting injectable Vocabria + Rekambys (branded as Cabenuva in the US Canada and Australia) following rapid viral suppression with daily Dovato (dolutegravir/lamivudine (DTG/3TC)). Additional r...
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Merck to Initiate Phase 3 Trials for Investigational Once-Monthly HIV Prevention Pill

RAHWAY, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the initiation of the EXPrESSIVE Phase 3 clinical trials, evaluating the safety and efficacy of MK-8527, an investigational once-monthly, oral nucleoside reverse transcriptase translocation inhibitor (NRTTI) for HIV pre-exposure prophylaxis (PrEP). The EXPrESSIVE-11 (MK-8527-011, NCT 07044297) trial will evaluate the safety and efficacy of MK-8527 among people with greater lik...