AstraZeneca

Solid tumors market projected to reach $375.4B by 2034 with 7.45% CAGR. Aethlon Medical activates Hemopurifier trial at Royal Adelaide Hospital for solid tumor patients resistant to anti-PD-1 therapies. Immuneering reports positive initial data for IMM-1-104 in pancreatic cancer. FDA approves new immunotherapy combinations for endometrial cancer from AstraZeneca, Merck, and GlaxoSmithKline. Roche's trastuzumab deruxtecan receives accelerated approval for HER2-positive solid tumors.

The NIAGARA study showed AstraZeneca's Imfinzi improved event-free survival in muscle-invasive bladder cancer, with a 25% reduction in death risk. This contrasts with Bristol Myers Squibb's Opdivo, which was previously approved for adjuvant use. The FDA's cautious stance on perioperative studies may delay Imfinzi's approval, despite its potential impact. Other ongoing trials, like KEYNOTE-866 and VOLGA, aim to further evaluate immunotherapies in this setting.

HIMALAYA trial results show AstraZeneca’s Imfinzi plus Imjudo reduced HCC death risk by 24% at 5 years, with 19.6% survival vs 9.4% with sorafenib.

AstraZeneca's Phase III HIMALAYA trial of Imfinzi (durvalumab) plus Imjudo (tremelimumab) showed a 24% reduction in death risk in advanced liver cancer patients, with 19.6% surviving five years, compared to 7% historically.

The article discusses the use of SSR (Server-Side Rendering) and its entry point in a bundle, focusing on the technical aspects of web development.

AstraZeneca's Phase III NIAGARA study shows perioperative Imfinzi regimen significantly reduces risk of disease progression, recurrence, and death by 32% and 25% respectively in muscle-invasive bladder cancer patients, with no new safety signals.

The HIMALAYA study's 5-year survival analysis shows 19.6% survival with STRIDE (durvalumab plus tremelimumab) vs 9.4% with sorafenib in unresectable hepatocellular carcinoma, with no new safety concerns.

AstraZeneca's Imfinzi shows positive results for bladder cancer; Apple receives FDA approval for hearing aid software on earbuds.

Sanofi and AstraZeneca are shipping Beyfortus doses to the U.S. ahead of the RSV season, with FDA clearance for a new manufacturing line. Despite initial supply issues, Sanofi aims to meet demand through additional production lines and a reservation system for private healthcare providers.

Sanofi is shipping BEYFORTUS doses in the US to ensure every eligible baby has access to immunization against RSV. A new filling line for BEYFORTUS has been approved by the FDA to expand manufacturing capacity. BEYFORTUS is the first long-acting monoclonal antibody for preventing RSV lower respiratory tract disease in newborns and infants up to 24 months.