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BMY News

Analysis of High-Yield Stocks in Pharma Sector

5h agoNASDAQ.COM

Top High-Yield Healthcare Stocks to Consider

6h agoFool

BioNTech's Strategic Shift and Clinical Progress

6h agoBenzinga

BioNTech Announces Earnings, But That's Not the Reason for the 17% Drop in Stock Price.

8h agoBarron's

Bristol Myers Squibb Reports Positive Phase 3 Trial Results

1d agoNASDAQ.COM

Bristol Myers Squibb's Cancer Drug Meets Key Trial Goals

1d agoseekingalpha

Bristol Myers Squibb Highlights from 2025 Earnings Report

1d agoNASDAQ.COM

Bristol Myers Squibb Maintains Positive Outlook for 2026

1d agoFool

BMY Events

03/09 07:10
Bristol Myers Squibb Announces Positive Interim Results from SUCCESSOR-2 Study
Bristol Myers Squibb announced positive interim Phase 3 results from the SUCCESSOR-2 study. In the trial, oral mezigdomide in combination with carfilzomib and dexamethasone (MeziKd) demonstrated statistically significant and clinically meaningful improvement in progression-free survival versus carfilzomib and dexamethasone alone in patients with relapsed or refractory multiple myeloma. Safety findings were consistent with the known profile of mezigdomide and the combination regimen. Patients will continue to be followed for survival and safety. "We are excited by these results, which underscore Bristol Myers Squibb's leadership in treating multiple myeloma and our unwavering commitment to patients living with this persistent and challenging disease," said Cristian Massacesi, executive vice president, chief medical officer and head of development at Bristol Myers Squibb. "Importantly, these findings reinforce the value of our CELMoD program and our targeted protein degradation platform, and strengthen our confidence in bringing forward effective, accessible oral treatment options for patients with difficult-to-treat blood cancers and potentially beyond."
03/08 22:30
KKR Plans to Sell CoolIT Systems for Over $3B
Catch up on the weekend's top five stories with this list compiled by The Fly: 1) KKR (KKR) is working on a sale of CoolIT Systems, hoping to fetch a price tag in excess of $3B, Oliver Barnes and Antoine Gara of The Financial Times reports, citing people familiar with the matter. This is a massive increase from the unit's $270M valuation when KKR bought a majority stake in 2023. 2) Dr. Vinay Prasad, who issued several controversial decisions, including having refused to accept Moderna's (MRNA) application for a new mRNA flu vaccine and refused an application for a Huntington's drug's review from UniQure (QURE), is leaving the agency at the end of April, reported The New York Times' Christina Jewett on Friday evening, citing a Health and Human Services spokesman. Publicly traded large-cap drugmakers include AstraZeneca (AZN), Bristol Myers (BMY), Eli Lilly (LLY), GSK (GSK), Johnson & Johnson (JNJ), Merck (MRK), Novartis (NVS), Pfizer (PFE), Roche (RHHBY) and Sanofi (SNY). Biotech stocks that could be impacted by the news include Sarepta (SRPT), Xencor (XNCR), PTC Therapeutics (PTCT), Biohaven (BHVN), Edgewise Therapeutics (EWTX), Design Therapeutics (DSGN), Ultragenyx (RARE), Avidity Biosciences (RNA), Dyne Therapeutics (DYN), Wave Life Sciences (WVE), MeiraGTx (MGTX), uniQure (QURE), Regenxbio (RGNX), Moderna (MRNA), Novavax (NVAX) and Lexeo Therapeutics (LXEO). 3) Plug Power (PLUG) plans to offer hydrogen electricity, as much as 250 megawatts, in an auction President Donald Trump is eager to make happen later this year, Will Wade and Naureen Malik of Bloomberg reports, citing chairman Andy Marsh. PJM Interconnection, which is facing power shortages due to surging consumption by data centers to power AI, has been urged by the Trump administration to hold an emergency auction to bolster supplies. 4) Prudential (PRU) disclosed yesterday that on March 6, the Prudential Gibraltar Financial Life Insurance Co., a subsidiary of Prudential Financial, issued a press release in Japan reporting instances of the unauthorized removal of information by certain employees of PGFL seconded to financial institutions in Japan. The investigation confirmed that 11 employees in total removed 379 instances of information at seven contracted agencies. The removed information pertained to operational matters such as sales performance at the assigned agencies. "After confirming the content of all cases with the agencies, no issues were identified that would raise concerns under the Unfair Competition Prevention Act, nor was there any inappropriate removal of contract information," Prudential Gibraltar Financial said. 5) Activist investor Starboard Value has built a stake in Lamb Weston (LW) and has been pushing to company to speed up improvements and cost cutting to boost stock performance, Lauren Thomas of The Wall Street Journal reports, citing people familiar with the matter. Starboard is now one of the largest shareholders in the company, the sources added.
03/08 17:00
Dr. Vinay Prasad to Leave Agency at End of April
Dr. Vinay Prasad, who issued several controversial decisions, including having refused to accept Moderna's (MRNA) application for a new mRNA flu vaccine and refused an application for a Huntington's drug's review from UniQure (QURE), is leaving the agency at the end of April, reported The New York Times' Christina Jewett on Friday evening, citing a Health and Human Services spokesman. Publicly traded large-cap drugmakers include AstraZeneca (AZN), Bristol Myers (BMY), Eli Lilly (LLY), GSK (GSK), Johnson & Johnson (JNJ), Merck (MRK), Novartis (NVS), Pfizer (PFE), Roche (RHHBY) and Sanofi (SNY). Biotech stocks that could be impacted by the news include Sarepta (SRPT), Xencor (XNCR), PTC Therapeutics (PTCT), Biohaven (BHVN), Edgewise Therapeutics (EWTX), Design Therapeutics (DSGN), Ultragenyx (RARE), Avidity Biosciences (RNA), Dyne Therapeutics (DYN), Wave Life Sciences (WVE), MeiraGTx (MGTX), uniQure (QURE), Regenxbio (RGNX), Moderna (MRNA), Novavax (NVAX) and Lexeo Therapeutics (LXEO).
03/08 13:10
Bristol Myers Squibb's Sotyktu Approved by FDA for Psoriatic Arthritis
Bristol Myers Squibb announced that the U.S. Food and Drug Administration, FDA, has approved Sotyktu for the treatment of adults with active psoriatic arthritis, PsA. This FDA approval is based on positive results from the pivotal POETYK PsA-1 and POETYK PsA-2 trials, which evaluated the efficacy and safety of Sotyktu 6 mg once daily in adults with active psoriatic arthritis. In both trials, treatment with Sotyktu resulted in significant improvement in disease activity, as measured by American College of Rheumatology 20 and Minimal Disease Activity, MDA, response. "The psoriatic disease community has been waiting for an additional oral treatment to address the debilitating joint and skin symptoms of this disease," said Steven Taylor, President & Chief Executive Officer of the Arthritis Foundation. "We welcome this new treatment option for people living with psoriatic arthritis."

BMY Monitor News

Bristol-Myers Squibb Reports Strong Q4 Earnings and Upgraded Outlook

Feb 06 2026

Bristol-Myers Squibb signs multi-year supply agreement with OXB

Feb 04 2026

Bristol-Myers Squibb Co reaches 20-day high amid sector rotation

Jan 07 2026

Bristol-Myers Squibb's Opdivo Receives FDA Priority Review

Dec 15 2025

Bristol-Myers Squibb's Opdivo Receives FDA Priority Review

Dec 12 2025

Bristol-Myers Squibb faces significant legal challenges

Dec 03 2025

BMY.N Hits 5-Day High Amid Investor Event Buzz

Nov 24 2025

BMY Shares Hit 5-Day Low After Trial Discontinuation

Nov 14 2025

BMY Earnings Analysis

Bristol-Myers Squibb Q1 2025 Earnings: Growth Strategy- Intellectia AI™
10 months ago
Strong Growth in Key Segments Marks Bristol Myers Squibb Q4 2024 Earnings Report - Intellectia AI™
1 years ago
Bristol Myers Squibb Reports Third Quarter 2024 Financial Results
1 years ago

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