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Moderna Inc.

Featured in 8 tracked stories · first seen

Situations

[ACTIVE] [HEALTH] [US] [ES]

Moderna and Merck melanoma vaccine clinical trials

9 clusters · 443 sources · last updated

Latest: Moderna reports positive Phase III results for personalized cancer vaccine

Moderna and Merck (MSD) have reported positive Phase 3 clinical trial results for intismeran autogene (also known as V940 or mRNA-4157), an experimental personalized mRNA cancer vaccine. The therapy is designed to target

[QUIET] [BUSINESS] [US] [CZ] [GB]

US stock market valuation and fiscal deficit concerns

12 clusters · 198 sources · last updated

Latest: S&P 500 faces high valuations amid historical September market weakness

In mid-August 2026, the S&P 500 reached new milestones, surpassing 7,800 points intraday before closing at 7,798.99. This surge was supported by the energy sector, healthcare, and financial services, alongside robust cor

[QUIET] [HEALTH] [CD] [CA] [GB]

Bundibugyo Ebola vaccine trials

4 clusters · 58 sources · last updated

Latest: Minapharm Group receives $16.5M for Bundibugyo ebola vaccine

Clinical efforts to address the Bundibugyo Ebola outbreak in the Democratic Republic of the Congo (DRC) continue to expand. The outbreak, which has seen infections surpass 4,000 cases, has prompted the WHO and Africa CDC

[QUIET] [BUSINESS] [DE] [US] [SG]

BioNTech restructuring, oncology shift, revenue cut

11 clusters · 42 sources · last updated

Latest: BioNTech halts personalized mRNA colorectal cancer vaccine trial

In August 2026, BioNTech significantly reduced its full-year revenue outlook to €1.6–1.9 billion, down from a previous target of €2.0–2.3 billion, citing declining COVID-19 vaccine demand and lost milestone payments. The

[QUIET] [HEALTH] [US]

Moderna mRNA flu vaccine US approval

4 clusters · 68 sources · last updated

Latest: Moderna's mFLUSIVA receives FDA approval as first mRNA flu vaccine

In early August 2026, the U.S. Food and Drug Administration (FDA) authorized Moderna’s mRNA-based seasonal influenza vaccine, mFlusiva. On 6 August, the agency granted full approval for adults aged 50–64, based on a late