Sanofi Secures Approval for Two Innovative Drugs Targeting Heart Disease and High Triglycerides
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 15 2026
0mins
Should l Buy SNY?
Source: NASDAQ.COM
- Drug Approvals: Sanofi's Myqorzo (aficamten) and Redemplo (plozasiran) have received approval from China's National Medical Products Administration, with Myqorzo targeting obstructive hypertrophic cardiomyopathy and Redemplo aimed at lowering triglyceride levels in patients with familial chylomicronaemia syndrome, marking a significant advancement in the cardiovascular space.
- Myqorzo Mechanism: Myqorzo is a selective small-molecule cardiac myosin inhibitor designed to improve functional capacity and relieve symptoms in patients with obstructive hypertrophic cardiomyopathy, which is the most common monogenic inherited cardiovascular disorder, and is expected to significantly enhance patient quality of life.
- Redemplo Mechanism: Redemplo is a small-interfering RNA (siRNA) medicine that suppresses the production of apoc-III to lower triglyceride levels in patients with familial chylomicronaemia syndrome, helping to reduce the risk of severe complications like acute pancreatitis, highlighting its clinical significance.
- Market Outlook: Sanofi acquired the rights to develop and commercialize Redemplo in Greater China in 2025, demonstrating the company's commitment to the region and is expected to further strengthen its market position in the cardiovascular sector with the launch of these two innovative drugs.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy SNY?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
Analyst Views on SNY
Wall Street analysts forecast SNY stock price to rise
5 Analyst Rating
2 Buy
3 Hold
0 Sell
Moderate Buy
Current: 47.030
Low
57.00
Averages
78.52
High
116.57
Current: 47.030
Low
57.00
Averages
78.52
High
116.57
About SNY
Sanofi SA is a France-based healthcare company based in France. The Company focuses on patient needs and engages in the research, development, manufacture, and marketing of therapeutic solutions. Its three operating segments are: Pharmaceuticals, Consumer Healthcare (CHC), and Vaccines. The Pharmaceuticals includes: Immunology, Multiple Sclerosis / Neurology, Oncology, Rare Diseases, Rare Blood Disorders, Cardiovascular, Diabetes, Established Prescription Products. The Vaccines segment comprises, for all geographical territories, the commercial operations of Sanofi Pasteur, together with research, development, and production activities dedicated to vaccines. The CHC segment comprises the commercial operations for Sanofi’s Consumer Healthcare products, together with research, development and production activities dedicated to those products. The Company’s products developed in collaboration or franchise include Dupixent, Aubagio, Lemtrada, Cerezyme, Lumizyme, Jevtana, Fabrazyme.
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.
Sanofi Faces Leadership Change Amid Drug Pipeline Challenges
- Leadership Transition: Sanofi announced that CEO Paul Hudson will depart on February 17, with Belén Garijo succeeding him, reflecting ongoing challenges in the company's drug pipeline and market performance, which may impact investor confidence.
- Sales Performance Fluctuations: While Sanofi's top drug Dupixent saw a 32.2% sales increase in Q4 2025, totaling €4.2 billion, vaccine sales declined by 2.5% to €2 billion, highlighting vulnerabilities in its product portfolio.
- Weak Stock Performance: Sanofi shares fell 0.68% in premarket trading to $46.71, trading 1.1% below the 20-day and 4% below the 100-day simple moving averages, indicating a bearish sentiment in the short term.
- Analyst Rating Changes: Despite an average price target of $61.50 and a “Buy” rating, recent downgrades from multiple firms suggest growing concerns about the company's future growth potential.
See More
Sanofi CEO Transition Amidst Challenges
- Executive Transition: Sanofi has decided not to renew Paul Hudson's director mandate, with his tenure as CEO ending on February 17, 2026, marking a significant governance shift after six years of leadership.
- Succession Plan: The Board has appointed Belén Garijo as the new CEO, set to officially take over after the Group's Annual General Meeting on April 29, 2026, aiming to enhance productivity and innovation in response to external pressures.
- Sales Performance Pressure: Despite Dupixent's sales increasing by 32.2% to €4.2 billion in Q4 2025, the company faces challenges in its vaccine segment, with overall vaccine sales declining by 2.5% to €2 billion, indicating fluctuating market demand.
- Future Therapy Development: Sanofi is developing amlitelimab as a potential successor to Dupixent, with preliminary data suggesting strong prospects in treating patients aged 12 and older with moderate-to-severe atopic dermatitis, potentially providing new growth avenues for the company.
See More
Sanofi Appoints New CEO Amid Board Changes
- Executive Change: Sanofi's Board of Directors has decided not to renew CEO Paul Hudson's mandate, with his last day set for February 17, indicating a significant leadership shift that may impact the company's strategic direction.
- New CEO Appointment: Belén Garijo has been appointed as the new CEO, set to officially take over after the Annual General Meeting on April 29, and her leadership is expected to bring fresh perspectives and experience, particularly in the pharmaceutical sector.
- Transition Management: Olivier Charmeil, Executive Vice President of General Medicines, will serve as Interim CEO during the transition period, ensuring operational continuity and minimizing uncertainties that may arise from the leadership change.
- Shareholder Vote: The company will hold a vote on Garijo's appointment to the Board and a proposed amendment to raise the CEO age limit, which could influence future executive selection criteria and corporate governance structures.
See More
Sanofi Board Appoints New CEO Amid Transition
- Executive Change: Sanofi's board has decided not to renew Paul Hudson's director mandate, who has served as CEO since September 2019, with his last working day set for February 17, 2026, indicating a significant leadership shift for the company.
- New CEO Appointment: Belén Garijo has been appointed as the new CEO, officially taking over after the Annual General Meeting on April 29, 2026, with her directorship subject to shareholder approval, reflecting the company's commitment to future leadership.
- Transition Arrangement: During the transition, Olivier Charmeil, the current executive vice president of general medicines, will serve as interim CEO, ensuring stability and continuity in operations during this leadership change to mitigate potential disruptions.
- Strategic Focus: As the new CEO, Garijo will concentrate on strengthening the execution of Sanofi's strategy, particularly in enhancing productivity, governance, and innovation in research and development, aiming to drive long-term growth in the competitive pharmaceutical market.
See More
NIH Discontinues Low-Dose Rivaroxaban Trial Amid Safety Concerns
- Trial Discontinuation Reason: The NIH has halted the low-dose rivaroxaban arm of the CAPTIVA stroke prevention trial due to an independent safety review that identified increased safety events, indicating that the treatment is unlikely to provide benefits for the 1,683 enrolled participants.
- Safety Evaluation: This decision follows recommendations from the Data Safety and Monitoring Board, which oversees participant safety, highlighting NIH's commitment to participant welfare and a cautious approach towards new therapies.
- Trial Design Context: The CAPTIVA trial aims to assess whether rivaroxaban or ticagrelor is superior to clopidogrel in reducing the rates of ischemic stroke, intracerebral hemorrhage, or vascular death, involving over 100 sites and spanning four years.
- Market Reaction: Despite the trial's discontinuation, Johnson & Johnson's stock rose by 1.09% to $240.95 at the time of publication, reflecting market confidence in the company's other business segments, although this event may negatively impact the outlook for related products.
See More
Sanofi Invests $30M in GluBio to Support Sickle Cell Candidates
- Strategic Investment: Sanofi's $30M investment in Chinese biotech startup GluBio aims to support the development of two sickle cell disease candidates, highlighting the company's commitment to innovative drug development.
- Exclusive Licensing Rights: Under the agreement, Sanofi secures the right of first refusal for the research, development, manufacturing, and commercialization of GLB-005 and GLB-007, enhancing its competitive position in the rare disease market.
- Clinical Trial Plans: GluBio is projected to begin Phase 1 trials for the candidates by the end of the year, which will add new potential to Sanofi's product pipeline and further strengthen its positioning in the biopharmaceutical sector.
- Market Outlook: Sanofi anticipates continued profitable growth over the next five years, and this investment not only aids in expanding its product portfolio but may also enhance overall company performance through successful drug launches.
See More
Sanofi Faces Leadership Change Amid Drug Pipeline Challenges
- Leadership Transition: Sanofi announced that CEO Paul Hudson will depart on February 17, with Belén Garijo succeeding him, reflecting ongoing challenges in the company's drug pipeline and market performance, which may impact investor confidence.
- Sales Performance Fluctuations: While Sanofi's top drug Dupixent saw a 32.2% sales increase in Q4 2025, totaling €4.2 billion, vaccine sales declined by 2.5% to €2 billion, highlighting vulnerabilities in its product portfolio.
- Weak Stock Performance: Sanofi shares fell 0.68% in premarket trading to $46.71, trading 1.1% below the 20-day and 4% below the 100-day simple moving averages, indicating a bearish sentiment in the short term.
- Analyst Rating Changes: Despite an average price target of $61.50 and a “Buy” rating, recent downgrades from multiple firms suggest growing concerns about the company's future growth potential.
See More
Sanofi CEO Transition Amidst Challenges
- Executive Transition: Sanofi has decided not to renew Paul Hudson's director mandate, with his tenure as CEO ending on February 17, 2026, marking a significant governance shift after six years of leadership.
- Succession Plan: The Board has appointed Belén Garijo as the new CEO, set to officially take over after the Group's Annual General Meeting on April 29, 2026, aiming to enhance productivity and innovation in response to external pressures.
- Sales Performance Pressure: Despite Dupixent's sales increasing by 32.2% to €4.2 billion in Q4 2025, the company faces challenges in its vaccine segment, with overall vaccine sales declining by 2.5% to €2 billion, indicating fluctuating market demand.
- Future Therapy Development: Sanofi is developing amlitelimab as a potential successor to Dupixent, with preliminary data suggesting strong prospects in treating patients aged 12 and older with moderate-to-severe atopic dermatitis, potentially providing new growth avenues for the company.
See More
Sanofi Appoints New CEO Amid Board Changes
- Executive Change: Sanofi's Board of Directors has decided not to renew CEO Paul Hudson's mandate, with his last day set for February 17, indicating a significant leadership shift that may impact the company's strategic direction.
- New CEO Appointment: Belén Garijo has been appointed as the new CEO, set to officially take over after the Annual General Meeting on April 29, and her leadership is expected to bring fresh perspectives and experience, particularly in the pharmaceutical sector.
- Transition Management: Olivier Charmeil, Executive Vice President of General Medicines, will serve as Interim CEO during the transition period, ensuring operational continuity and minimizing uncertainties that may arise from the leadership change.
- Shareholder Vote: The company will hold a vote on Garijo's appointment to the Board and a proposed amendment to raise the CEO age limit, which could influence future executive selection criteria and corporate governance structures.
See More
Sanofi Board Appoints New CEO Amid Transition
- Executive Change: Sanofi's board has decided not to renew Paul Hudson's director mandate, who has served as CEO since September 2019, with his last working day set for February 17, 2026, indicating a significant leadership shift for the company.
- New CEO Appointment: Belén Garijo has been appointed as the new CEO, officially taking over after the Annual General Meeting on April 29, 2026, with her directorship subject to shareholder approval, reflecting the company's commitment to future leadership.
- Transition Arrangement: During the transition, Olivier Charmeil, the current executive vice president of general medicines, will serve as interim CEO, ensuring stability and continuity in operations during this leadership change to mitigate potential disruptions.
- Strategic Focus: As the new CEO, Garijo will concentrate on strengthening the execution of Sanofi's strategy, particularly in enhancing productivity, governance, and innovation in research and development, aiming to drive long-term growth in the competitive pharmaceutical market.
See More
NIH Discontinues Low-Dose Rivaroxaban Trial Amid Safety Concerns
- Trial Discontinuation Reason: The NIH has halted the low-dose rivaroxaban arm of the CAPTIVA stroke prevention trial due to an independent safety review that identified increased safety events, indicating that the treatment is unlikely to provide benefits for the 1,683 enrolled participants.
- Safety Evaluation: This decision follows recommendations from the Data Safety and Monitoring Board, which oversees participant safety, highlighting NIH's commitment to participant welfare and a cautious approach towards new therapies.
- Trial Design Context: The CAPTIVA trial aims to assess whether rivaroxaban or ticagrelor is superior to clopidogrel in reducing the rates of ischemic stroke, intracerebral hemorrhage, or vascular death, involving over 100 sites and spanning four years.
- Market Reaction: Despite the trial's discontinuation, Johnson & Johnson's stock rose by 1.09% to $240.95 at the time of publication, reflecting market confidence in the company's other business segments, although this event may negatively impact the outlook for related products.
See More
Sanofi Invests $30M in GluBio to Support Sickle Cell Candidates
- Strategic Investment: Sanofi's $30M investment in Chinese biotech startup GluBio aims to support the development of two sickle cell disease candidates, highlighting the company's commitment to innovative drug development.
- Exclusive Licensing Rights: Under the agreement, Sanofi secures the right of first refusal for the research, development, manufacturing, and commercialization of GLB-005 and GLB-007, enhancing its competitive position in the rare disease market.
- Clinical Trial Plans: GluBio is projected to begin Phase 1 trials for the candidates by the end of the year, which will add new potential to Sanofi's product pipeline and further strengthen its positioning in the biopharmaceutical sector.
- Market Outlook: Sanofi anticipates continued profitable growth over the next five years, and this investment not only aids in expanding its product portfolio but may also enhance overall company performance through successful drug launches.
See More
