Fortinet Shares Surge 7% After TD Cowen Upgrade to Buy
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 23 2026
0mins
Should l Buy MRNA?
Source: CNBC
- Stock Surge: Fortinet shares jumped over 7% after TD Cowen upgraded the stock from hold to buy, indicating increased market confidence in its future performance, particularly as rising memory prices are expected to have a lesser impact than anticipated.
- Clinical Trial Setback: Bausch Health's stock fell 9% after one of its experimental treatments for hepatic encephalopathy missed targets in a late-stage clinical trial, potentially affecting the company's future product pipeline and market competitiveness.
- Weak Earnings Report: Intel shares dropped 16% following mixed fourth-quarter results and a weak forecast, with expected first-quarter revenue between $11.7 billion and $12.7 billion, failing to meet analyst expectations, which may lead to decreased investor confidence.
- Acquisition Deal: Clorox shares rose nearly 3% after agreeing to acquire Gojo Industries for $2.25 billion, and despite the financial impact of the acquisition, the company reaffirmed its outlook for 2026.
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Analyst Views on MRNA
Wall Street analysts forecast MRNA stock price to fall
20 Analyst Rating
1 Buy
16 Hold
3 Sell
Hold
Current: 55.740
Low
17.00
Averages
32.47
High
63.00
Current: 55.740
Low
17.00
Averages
32.47
High
63.00
About MRNA
Moderna, Inc. is a biotechnology company. The Company is advancing a new class of medicines made of messenger ribonucleic acid (mRNA). It is developing therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases and autoimmune diseases. mRNA medicines are designed to direct the body’s cells to produce intracellular, membrane or secreted proteins that have a therapeutic or preventive benefit with the potential to address a spectrum of diseases. The Company’s diverse development pipeline consists of 44 therapeutic and vaccine programs, 11 of which are in late-stage development. Its commercial products include Spikevax (its COVID vaccine) and mRESVIA (its respiratory syncytial virus (RSV) vaccine). Additionally, it has achieved four positive Phase III data readouts for its COVID vaccine (mRNA-1283), its RSV vaccine for high-risk adults aged 18 to 59 (mRNA-1345), its seasonal flu+COVID vaccine (mRNA-1083), and its seasonal flu vaccine (mRNA-1010).
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Executive Transition: Co-founders Ugur Sahin and Özlem Türeci plan to lead a new venture by the end of 2026, prompting BioNTech's Supervisory Board to initiate a search for successors, which may impact the company's strategic direction and market confidence.
- Clinical Trial Progress: BioNTech expects to have 15 ongoing Phase 3 clinical trials by the end of 2026, covering major cancer types, with the resulting data informing regulatory and launch plans, potentially enhancing the company's competitiveness in oncology.
- Stock Performance: BioNTech's shares have decreased by 3.03% over the past 12 months, currently trading at $87.60, which is 18% below its 100-day simple moving average, reflecting a bearish market sentiment that could affect investor confidence.
- Market Momentum Analysis: With a Benzinga Edge score of 19.82 indicating weak momentum, BioNTech's stock is underperforming the broader market, although the strategic pivot may present future growth opportunities, current market sentiment remains negative.
See More
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- Quarterly Loss: BioNTech reported a significant quarterly loss, indicating challenges in its operations.
- Leadership Changes: The company announced the departure of its co-founders, marking a significant shift in its leadership structure.
See More
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- Leadership Change: Dr. Vinay Prasad, head of the FDA's Center for Biologics Evaluation and Research, confirmed his departure in April, prompting market interest, particularly as Moderna's stock rises due to his controversial drug review decisions.
- Positive Market Reaction: Analyst from William Blair noted that investors are optimistic about Prasad's exit, believing it will benefit regulatory approvals for rare disease drugs, especially those utilizing single-arm studies and external controls.
- Potential Gains for Moderna: With Prasad's departure, Moderna's mRNA-1010 vaccine could qualify for full approval in adults aged 65 and older, potentially sparing the company from conducting an additional costly vaccine efficacy study.
- Stock Price Increases: Following the news of Prasad's resignation, stocks of Solid Biosciences and Capricor Therapeutics rose by 12.15% and 9.07%, respectively, indicating increased market confidence in rare disease treatments.
See More
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- Oil Price Surge: U.S. crude futures have surged above $100 per barrel for the first time since mid-2022, driven by Iran's threats to close the Strait of Hormuz, with a staggering 35.6% increase last week marking the largest weekly gain in futures history, which has directly impacted the stock market, leading to the Dow's worst week in nearly a year.
- Economic Pressure Intensifies: The rising oil prices have prompted Democrats to frame the conflict as a catalyst for increased living costs, potentially affecting the upcoming midterm elections negatively, while Republicans hope for a swift resolution to avoid economic fallout, highlighting the intersection of politics and economics.
- FDA Leadership Change: Vinay Prasad, the FDA's vaccine chief, announced his resignation effective at the end of April following widespread criticism of his decisions from the biotech and pharmaceutical sectors, illustrating the challenges and pressures regulatory bodies face in managing public health crises.
- Changing Canadian Consumption Trends: Canadians continue to boycott U.S. goods, with data indicating a shift towards domestic brands and increased local tourism spending, a trend that could significantly impact Canada's GDP and inflation rates in the long term.
See More
uniQure Shares Surge Following FDA Official's Departure
- Significant Stock Surge: uniQure's shares surged 31.39% to $18.75 in premarket trading following the announcement of FDA's biologics division head Vinay Prasad's resignation, extending a 33.99% increase from Friday, indicating strong market optimism about the company's future prospects.
- Regulatory Decision Controversy: During Prasad's tenure, he faced criticism for the FDA's rejection of uniQure's Huntington's disease gene therapy application, as the agency recommended a prospective randomized controlled study, adding regulatory uncertainty that could impact uniQure's market outlook.
- Clinical Trial Challenges: The FDA previously indicated that uniQure could pursue accelerated approval without a placebo control due to difficulties in enrolling Huntington's disease patients, reflecting regulatory flexibility for rare diseases, yet this has sparked ongoing debates about clinical trial design.
- Strong Market Reaction: Following the news of Prasad's departure, uniQure's shares reportedly jumped as much as 70% in after-hours trading, reflecting investor expectations for a potential easing of tensions between the company and the FDA, which could pave the way for future product approvals.
See More
Dr. Vinay Prasad to Depart FDA Amid Controversial Tenure
- Leadership Change: Dr. Vinay Prasad, head of the FDA's Center for Biologics Evaluation and Research, is set to leave at the end of April, which may impact the agency's policy direction on vaccines and biotech drugs, particularly as new policies he implemented are still unfolding.
- Controversial Tenure: Prasad's tenure has been contentious, marked by staff complaints about his management style; however, his rehiring in August 2025 indicates a divide within the FDA regarding his leadership, potentially affecting the agency's stability.
- Vaccine Standards Reform: His departure follows strict reforms in vaccine standards at the FDA, sparking widespread industry debate that could have lasting implications for future vaccine approval processes, especially given his critical stance on the biopharmaceutical industry.
- Regulatory Direction Debate: Prasad's return ignited discussions about the FDA's regulatory direction, particularly due to his criticisms of certain FDA approval pathways, which may lead to decreased confidence in the agency's future policies and impact strategic planning for biopharmaceutical companies.
See More
