Pfizer Announces New Progress on BRAFTOVI Trial
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 2 hours ago
0mins
Pfizer announced detailed progression-free and overall survival results from Cohort 3, a randomized cohort of the Phase 3 Breakwater trial, evaluating Bratovi in combination with cetuximab and Folfiri versus Folfiri with or without bevacizumab in patients with previously untreated metastatic colorectal cancer, mCRC, with a BRAF V600E mutation. These results will be presented today in a late-breaking oral presentation at the 2026 American Society of Clinical Oncology, ASCO, Annual Meeting and simultaneously published in the Annals of Oncology. As previously reported, Cohort 3 met its primary endpoint of objective response rate by blinded independent central review. Results for the key secondary endpoint of progression-free survival by BICR, being presented at ASCO, show median PFS was nearly doubled with the BRAFTOVI combination regimen versus the comparator.
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Analyst Views on PFE
Wall Street analysts forecast PFE stock price to rise
16 Analyst Rating
5 Buy
11 Hold
0 Sell
Moderate Buy
Current: 26.140
Low
24.00
Averages
28.56
High
35.00
Current: 26.140
Low
24.00
Averages
28.56
High
35.00
About PFE
Pfizer Inc. is a research-based, global biopharmaceutical company. The Company is engaged in the discovery, development, manufacture, marketing, sale and distribution of biopharmaceutical products worldwide. Its Biopharma segment includes the Pfizer U.S. Commercial Division, and the Pfizer International Commercial Division. Its product categories include oncology, primary care and specialty care. Its oncology products include Ibrance, Xtandi, Padcev, Adcetris, Inlyta, Lorbrena, Bosulif, Tukysa, Braftovi, Mektovi, Orgovyx, Elrexfio, Tivdak and Talzenna. Its primary care products include Eliquis, Nurtec ODT/Vydura, Zavzpret, the Prevnar family, Comirnaty, Abrysvo, FSME/IMMUN-TicoVac, Nimenrix, Trumenba, and Paxlovid. Its specialty care products include Xeljanz, Enbrel (outside the United States and Canada), Inflectra, Abrilada, Cibinqo, Litfulo, Eucrisa, Velsipity, the Vyndaqel family, Genotropin, and others. Its PF-08653944 is an ultra-long-acting fully biased GLP-1 receptor agonist.
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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See More
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- Long History: Founded in 1849, Pfizer has survived over a century in the highly competitive pharmaceutical industry, with a corporate ethos emphasizing resilience in adversity, which instills confidence in investors.
- Stock Price Decline: Pfizer's stock has dropped over 50% due to a retraction in pandemic-related vaccine demand, following a significant price spike, presenting a potential buying opportunity for long-term investors.
- Patent Expiration Risks: The company faces risks from the expiration of patents on key drugs, with several set to expire by 2028, leading to concerns about declining sales and investor apprehension.
- Innovation and Investment Opportunities: Despite challenges, Pfizer is actively developing new drugs, including vaccines and oncology treatments, with plans for up to 20 pivotal studies in 2026, indicating its long-term investment potential amidst industry dynamics.
See More
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- Long-Standing Company: Founded in 1849, Pfizer has survived over a century in the highly competitive pharmaceutical industry, emphasizing a corporate ethos of resilience that provides long-term investors with confidence in its potential recovery.
- Significant Stock Decline: Pfizer's stock has dropped over 50% from pandemic highs as COVID vaccine demand wanes, presenting a potential buying opportunity for long-term investors amid current negative market sentiment.
- Patent Expiration Risks: The company faces significant revenue risks due to the expiration of patents on key drugs, with multiple patents set to expire by 2028, leading to an influx of generics that could impact sales and investor confidence.
- Innovation and Acquisitions: Rather than retreating, Pfizer is actively pursuing innovation by acquiring competitors for more attractive GLP-1 drugs and planning up to 20 pivotal studies in 2026, demonstrating its commitment to medical advancement despite challenges.
See More
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- Ceasefire Agreement Impact: The temporary 60-day ceasefire agreement between the US and Iran alleviated energy price concerns for oil-importing nations, contributing to a 1.2% rise in the S&P 500 index.
- AI-Driven Optimism: Renewed optimism surrounding artificial intelligence and related technologies propelled the Nasdaq index up by 2%, indicating strong performance in tech stocks and a recovery in investor confidence.
- European Market Decline: In contrast to the US gains, European equities fell, with the STOXX index down 0.5%, reflecting concerns over the eurozone economic outlook, particularly after lower-than-expected inflation rates in Germany and France.
- Asian Market Divergence: Chinese markets dropped by 1.4%, while Japan's Nikkei 225 rose by 2.2%, highlighting a lack of synchronization in regional economic recovery, especially given Japan's strong retail sales and industrial output figures.
See More
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- Significant Efficacy Improvement: In Cohort 3 of the BREAKWATER trial, the BRAFTOVI combination therapy achieved a median progression-free survival (PFS) of 15.2 months, nearly doubling the comparator's 8.3 months, indicating a potential shift in treatment paradigms.
- Survival Rate Enhancement: Patients receiving the BRAFTOVI regimen experienced a 44% reduction in death risk, with an expected 72% survival rate at 18 months compared to 54.5% in the comparator group, highlighting the clinical significance of this combination therapy in extending survival.
- Stable Safety Profile: The safety profile of BRAFTOVI in combination with other agents remained consistent with known drug characteristics, with no new safety signals identified; 70.4% of patients experienced grade 3 adverse events, lower than the 80.9% in the comparator group, suggesting better tolerability.
- Treatment Discontinuation Rates: Treatment discontinuation due to adverse events was reported in 15.5% of patients on the BRAFTOVI regimen versus 10.3% for the comparator, indicating a need to monitor patient tolerability and treatment continuity in clinical practice.
See More
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- Clinical Trial Results: The experimental drug ivonescimab from Akeso and Summit Therapeutics demonstrated a 34% reduction in death risk in late-stage trials, extending median survival by four months for patients with squamous non-small-cell lung cancer when combined with chemotherapy, indicating its potential in difficult-to-treat populations.
- Global Research Plans: The results from the Phase 3 trial conducted in China have garnered attention, and while a global Phase 3 study is ongoing, the applicability of the Chinese data to other populations remains uncertain, highlighting implications for future market dynamics.
- Market Reaction: Since Summit Therapeutics announced ivonescimab's superiority over Keytruda in a separate trial, its stock has surged nearly 600%, yet recent declines due to concerns over global efficacy reflect investor divisions regarding the drug's prospects.
- Safety Considerations: The trial revealed a bleeding incidence of nearly 25% in the ivonescimab group, double that of the control group, raising safety concerns despite fewer severe cases, which may impact market acceptance.
See More
Analysts' Negative Outlook on Pfizer
- Analyst Rating Discrepancy: Among 29 analysts, only 2 have a strong buy rating for Pfizer, with 9 at buy, while the rest are hold or sell, indicating over 60% of analysts suggest a cautious view, reflecting a negative market perception of the company.
- Stock Price Decline Impact: Pfizer's stock has fallen over 50% from its 2021 peak, leading to investor disappointment regarding its business outlook, particularly with upcoming patent expirations that will significantly impact revenue from key drugs like Eliquis and Vyndaqel.
- New Drug Development Challenges: Pfizer's decision to drop its internally developed GLP-1 drug in the first half of 2025 has hindered its entry into a high-demand drug category, resulting in diminished investor confidence in its future product pipeline and negatively affecting the company's market image.
- Rising Dividend Yield: Despite Pfizer's dividend yield rising to 6.6%, well above the market average of 1.1%, its payout ratio exceeds 100%, yet the company remains committed to supporting dividend payments, demonstrating a determination to maintain shareholder returns during challenging times.
See More
