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Meta Platforms Inc. Secures Nearly 800 MW Clean Energy in New Invenergy Partnership

Invenergy to Provide Meta With Nearly 800 Mw, Supporting Data Center Operations

THOMSON REUTERS

Invenergy - Agreements With Meta Contracted Through Four Invenergy Facilities in U.S.

THOMSON REUTERS

Pfizer's bleeding disorder therapy meets main goal in patients with certain antibodies

Pfizer Announces Positive Phase 3 Results for HYMPAVZI in Hemophilia A or B with Inhibitors, Showcasing Significant Reduction in Bleeding Rates

Pfizer Inc - to Initiate Regulatory Filings for Hympavzi

THOMSON REUTERS

Pfizer Inc - Hympavzi Generally Well-Tolerated With No Deaths or Thromboembolic Events

THOMSON REUTERS

Pfizer Inc - Hympavzi Shows 93% Reduction in Annualized Bleeding Rate

THOMSON REUTERS

Pfizer Inc - Hympavzi Demonstrates Superiority in Reducing Bleeding Outcomes

THOMSON REUTERS

Pfizer Announces Positive Topline Phase 3 Results for Hympavzi™ in Hemophilia a or B With Inhibitors

THOMSON REUTERS

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BRIEF-Meta Poaches Three OpenAI Researchers - WSJ

Meta Has Hired Lucas Beyer, Alexander Kolesnikov and Xiaohua Zhai for Its Superintelligence Effort- WSJ

THOMSON REUTERS

Meta Poaches Three OpenAI Researchers - WSJ

THOMSON REUTERS

Why Adobe’s (ADBE) Steady Growth Can’t Silence the Stock Bears

The Ultimate Growth Stock to Buy With $1,000 Right Now

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Pfizer PFE.N said on Thursday its hemophilia therapy, Hympavzi, met the main goal of a late-stage study in patients with certain types of antibodies.  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Pfizer Inc. has announced positive topline results from the Phase 3 BASIS study evaluating HYMPAVZI  for adults and adolescents with hemophilia A or B with inhibitors. The study demonstrated a statistically significant and clinically meaningful reduction in annualized bleeding rate compared to on-demand treatment in patients aged 12 and older. HYMPAVZI, administered as a once-weekly subcutaneous injection, showed a generally well-tolerated safety profile. Results from the full Phase 3 dataset are currently being analyzed, with additional data to be presented at upcoming medical meetings. Pfizer intends to discuss these findings with regulatory authorities to initiate filings for HYMPAVZI's approval for use in patients with hemophilia with inhibitors.Disclaimer: This news brief was created by Public Technologies  using generative artificial 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