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Sangamo Therapeutics (SGMO) & Sanofi (SNY) Company, Bioverativ Inc., Report FDA Acceptance of IND Application for Gene-Edited Cell Therapy BIVV003 to Treat Sickle Cell Disease
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Sanofi (SNY) & Regeneron (REGN) Report Dupixent (dupilumab) Showed Positive Phase 3 Results in Adolescents with Inadequately Controlled Moderate-to-Severe Atopic Dermatitis
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Sanofi: Dupixent® (dupilumab) showed positive Phase 3 results in adolescents with inadequately controlled moderate-to-severe atopic dermatitis
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Sanofi: Dupixent® (dupilumab) showed positive Phase 3 results in adolescents with inadequately controlled moderate-to-severe atopic dermatitis
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Sanofi: Dupixent® (dupilumab) showed positive Phase 3 results in adolescents with inadequately controlled moderate-to-severe atopic dermatitis
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Sanofi: Dupixent® (dupilumab) showed positive Phase 3 results in adolescents with inadequately controlled moderate-to-severe atopic dermatitis
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Sanofi (SNY) and Regeneron (REGN) to Lower Net Price of Praluent; Praluent will become Exclusive PCSK9 inhibitor Therapy on Express Scripts (ESRX) National Formulary
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Sanofi and Regeneron to lower net price of Praluent® (alirocumab) Injection in exchange for straightforward, more affordable patient access for Express Scripts patients
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Regeneron (REGN) Reports Acceptance for FDA Priority Review of BLA for Cemiplimab
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Sanofi: FDA to Conduct Priority Review of Cemiplimab as a Potential Treatment for Advanced Cutaneous Squamous Cell Carcinoma
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Sanofi: FDA to Conduct Priority Review of Cemiplimab as a Potential Treatment for Advanced Cutaneous Squamous Cell Carcinoma
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FDA to Conduct Priority Review of Cemiplimab as a Potential Treatment for Advanced Cutaneous Squamous Cell Carcinoma
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Regeneron (REGN) & Sanofi (SNY) Report EMA to Review Cemiplimab as Potential Treatment for Advanced Cutaneous Squamous Cell Carcinoma
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Regeneron (REGN) & Sanofi (SNY) Report EMA to Review DUPIXENT (dupilumab) as Potential Treatment for Inadequately Controlled Moderate-to-Severe Asthma
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Sanofi: EMA to review cemiplimab as a potential treatment for advanced cutaneous squamous cell carcinoma
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Sanofi: EMA to review Dupixent® (dupilumab) as potential treatment for inadequately controlled moderate-to-severe asthma
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Regeneron (REGN) and Sanofi (SNY) Announce Praluent Met Primary Endpoint of Reducing Cardiovascular Events
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Sanofi and Regeneron announce plans to make Praluent® more accessible and affordable for patients with the greatest health risk and unmet need
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Sanofi and Regeneron announce plans to make Praluent® more accessible and affordable for patients with the greatest health risk and unmet need
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Sanofi and Regeneron announce plans to make Praluent® more accessible and affordable for patients with the greatest health risk and unmet need
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Sanofi and Regeneron announce plans to make Praluent® more accessible and affordable for patients with the greatest health risk and unmet need
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Sanofi: Praluent® (alirocumab) significantly reduced risk of cardiovascular events in high-risk patients, and was associated with lower death rate
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Sanofi: Praluent® (alirocumab) significantly reduced risk of cardiovascular events in high-risk patients, and was associated with lower death rate
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Sanofi: Praluent® (alirocumab) significantly reduced risk of cardiovascular events in high-risk patients, and was associated with lower death rate
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Praluent® (alirocumab) Injection significantly reduced risk of cardiovascular events in high-risk patients, and was associated with lower death rate
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Regeneron (REGN) & Sanofi (SNY) Announce DUPIXENT Accepted for FDA Review
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Sanofi : FDA to review Dupixent® (dupilumab) as potential treatment for moderate-to-severe asthma
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Sanofi : FDA to review Dupixent® (dupilumab) as potential treatment for moderate-to-severe asthma
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Sanofi : FDA to review Dupixent® (dupilumab) as potential treatment for moderate-to-severe asthma
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Sanofi (SNY) Commences Tender Offer for Acquisition of Bioverativ (BIVV)
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Sanofi Commences Tender Offer for Acquisition of Bioverativ Inc.
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Sanofi Commences Tender Offer for Acquisition of Bioverativ Inc.
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Sanofi Commences Tender Offer for Acquisition of Bioverativ Inc.
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Pre-Open Movers 01/22: (BIVV) (JUNO) (ARRY) Higher; (SANM) (TEVA) (TWTR) Lower (more...)
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Sanofi (SNY) to Acquire Bioverativ (BIVV) for $11.6B
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Sanofi to Acquire Bioverativ for $11.6 Billion
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Sanofi to Acquire Bioverativ for $11.6 Billion
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Sanofi (SNY), Regeneron (REGN) to accelerate, expand investment for cemiplimab and dupilumab development programs
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Sanofi and Regeneron to accelerate and expand investment for cemiplimab and dupilumab development programs
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Sanofi and Regeneron to accelerate and expand investment for cemiplimab and dupilumab development programs
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Sanofi and Regeneron to accelerate and expand investment for cemiplimab and dupilumab development programs
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Evotech & Aperion Announce First Milestone Achievement in Immuno-Oncology Alliance with Sanofi (SNY)
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Alnylam Pharma (ALNY) and Sanofi (SNY) Report Strategic Restructuring of RNAi Therapeutics Rare Disease Alliance
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Sanofi and Alnylam enter into strategic restructuring of RNAi therapeutics rare disease alliance
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Sanofi and Alnylam enter into strategic restructuring of RNAi therapeutics rare disease alliance
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Sanofi and Alnylam enter into strategic restructuring of RNAi therapeutics rare disease alliance
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Sanofi (SNY) and Alnylam (ALNY) Submit EU Marketing Authorization Application for Patisiran to Treat hATTR amyloidosis
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Alnylam Pharma (ALNY) & Sanofi (SNY) Announce Marketing Authorisation Application to EMA for Patisiran for Treatment of Hereditary ATTR Amyloidosis
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Sanofi and Alnylam submit Marketing Authorization Application to the European Medicines Agency for patisiran for the treatment of hereditary ATTR amyloidosis
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Sanofi and Alnylam submit Marketing Authorization Application to the European Medicines Agency for patisiran for the treatment of hereditary ATTR amyloidosis

