EU Approves Sarclisa Subcutaneous Injection for Multiple Myeloma
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jun 08 2026
0mins
Source: NASDAQ.COM
- Regulatory Approval: The European Commission has approved Sarclisa (isatuximab) subcutaneous injection in combination with standard care regimens for all existing indications, marking a significant advancement in multiple myeloma treatment.
- Innovative Administration: Sarclisa is the first anticancer therapy in the EU to be administered via an on-body injector (OBI) and manual subcutaneous injection, providing flexibility for patients to receive treatment at home or in outpatient settings, enhancing patient experience.
- Market Performance: Since its launch in 2020, Sarclisa has been prescribed globally, with the IV formulation approved for four indications in the EU, including combinations with bortezomib, lenalidomide, and dexamethasone, showcasing its broad application potential in multiple myeloma therapy.
- Stock Movement: Sanofi (SNY) closed at $45.02 on June 5, up 1.44%, but slipped slightly to $44.75 in after-hours trading on June 7, reflecting a cautious market response to the new drug approval.
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: 42.500
Low
57.00
Averages
79.36
High
119.07
Current: 42.500
Low
57.00
Averages
79.36
High
119.07
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.
Japan Approves Sarclisa Subcutaneous Injection for Multiple Myeloma
- New Drug Approval: French pharmaceutical giant Sanofi announced that its Sarclisa (isatuximab) subcutaneous formulation has been approved in Japan for multiple myeloma patients, marking a significant advancement in the oncology sector.
- Expanded Indications: The approval for Sarclisa SC includes its use in combination with approved standard treatment regimens, such as with pomalidomide and dexamethasone for relapsed or refractory multiple myeloma, and with bortezomib, lenalidomide, and dexamethasone for newly diagnosed patients, showcasing its broad clinical application potential.
- Clinical Research Support: This approval is based on results from the IRAKLIA phase 3 study, which demonstrated non-inferiority of Sarclisa SC compared to intravenous administration in treating relapsed or refractory multiple myeloma, further enhancing its market competitiveness.
- Innovative Delivery Method: Sanofi's CirCLIQ on-body injector (OBI) is currently under review in Japan, and if approved, Sarclisa SC will become the first anticancer treatment administered via an OBI, significantly improving patient convenience and adherence to treatment.
See More
Denali Sells Rare Pediatric Disease Priority Review Voucher for $195 Million
- Significant Transaction: Denali Therapeutics announced the sale of its Rare Pediatric Disease Priority Review Voucher (PRV) for $195 million, providing a substantial non-dilutive capital infusion that significantly strengthens its financial position.
- Product Background: The PRV was granted following the FDA's accelerated approval of Avlayah (tividenofusp alfa-eknm) in March 2026 for treating Hunter syndrome, highlighting the drug's market potential and the company's competitiveness in the rare disease sector.
- Advancing Clinical Portfolio: The capital infusion will aid Denali in advancing its broad Transport Vehicle-enabled clinical portfolio focused on lysosomal storage disorders and neurodegenerative diseases, further solidifying its position in the biopharmaceutical industry.
- Collaborations and R&D: Denali collaborates with pharmaceutical giants like Sanofi, Biogen, and Takeda to develop various candidates, and despite the discontinuation of the BIIB122 project with Biogen due to unmet expectations, the company will continue to independently advance other key studies, demonstrating resilience and promising prospects in its R&D efforts.
See More
FDA Approves Expanded Use of Sanofi's Diabetes Therapy Tzield
- Indication Expansion: The FDA has approved Sanofi's Tzield therapy for expanded use in stage 3 diabetes patients, aiming to delay insulin production decline in children aged 8 to 17, marking a significant broadening of treatment scope.
- Clinical Trial Support: This approval is backed by data from the PROTECT Phase 3 trial, which demonstrated that patients on Tzield experienced a significant slowdown in C-peptide decline, indicating its effectiveness in delaying diabetes progression.
- Accelerated Approval Pathway: Tzield's accelerated approval allows it to delay the onset of stage 3 diabetes in stage 2 patients, reflecting the FDA's recognition of the therapy's potential benefits, which could lead to greater market opportunities for Sanofi.
- Follow-up Research Plans: Sanofi is currently enrolling patients in the BETA-PRESERVE Phase 3 study, aiming to convert the accelerated approval into standard approval, further solidifying its position in the diabetes treatment landscape.
See More
Sanofi's Tzield Receives FDA Accelerated Approval
- FDA Accelerated Approval: Sanofi's Tzield (teplizumab-mzwv) has received FDA accelerated approval for delaying endogenous insulin production decline in children aged 8 to 17 recently diagnosed with stage 3 type 1 diabetes, marking a significant advancement in diabetes treatment.
- Clinical Research Support: This approval is based on results from the PROTECT phase 3 study and additional data from a global clinical development program involving over 900 patients, demonstrating Tzield's effectiveness in delaying insulin decline, potentially opening new market opportunities for the company.
- Adverse Reaction Concerns: Common adverse reactions associated with Tzield include lymphopenia, vomiting, and rash, with serious events such as cytokine release syndrome and viral reactivation risks, which may affect patient willingness to use the drug and market acceptance.
- Global Regulatory Dynamics: Beyond the U.S., Tzield has also been approved in several countries including the UK, EU, and China, indicating its potential in global markets, while facing ongoing regulatory reviews in other jurisdictions that could impact future sales growth.
See More
Dianthus Therapeutics Receives Strong Buy Rating Following Positive Trial Results
- Clinical Trial Success: Dianthus Therapeutics reported that 75% of patients in its trial for claseprubart, aimed at chronic inflammatory demyelinating polyneuropathy (CIDP), showed significant improvement, exceeding the company's expectation of 50%, thereby enhancing its competitive position in the market.
- Positive Market Reaction: Following the announcement of favorable clinical data, Dianthus's stock surged 8% on Friday, marking its best performance since March, indicating strong investor confidence in its future potential.
- Analyst Rating Maintained: Investment bank Raymond James reaffirmed its 'Strong Buy' rating on Dianthus, keeping the price target at $125 per share, reflecting a positive market outlook, especially in comparison to competing drugs from Sanofi.
- Future Guidance: Dianthus expects to provide guidance on the timing of Part B top-line results by the end of 2026, further increasing investor interest in its research progress, particularly in the treatment of CIDP and other neurological disorders.
See More
Biotech Sector Sees Surge in FDA and Global Approvals
- FDA Approval Boosts Innovation: Guardant Health (GH) secured FDA approval for its Guardant360 CDx liquid biopsy test as a companion diagnostic for Boehringer Ingelheim's HERNEXEOS, highlighting the growing importance of liquid biopsy in advanced cancer treatment, which is expected to drive GH's market share growth.
- Therapy Expansion: Eli Lilly (LLY) received FDA approval for an every-eight-week maintenance dose of EBGLYSS, with Q1 2026 sales surging 141% to $145 million, reflecting strong demand in its immunology portfolio and further solidifying the company's market position.
- China Market Breakthrough: Vor Bio (VOR) announced that Telitacicept received approval from China's NMPA, becoming the only approved therapy for Sjögren's disease in the country, supported by positive Phase 3 trial data, which is expected to significantly improve patient quality of life and expand market reach.
- EU Approval for New Therapy: Sanofi (SNY) secured European Commission approval for Sarclisa in newly diagnosed multiple myeloma patients, based on Phase 3 IRAKLIA trial results, which is expected to enhance Sarclisa's application range and strengthen the company's competitiveness in blood cancer treatment.
See More
Japan Approves Sarclisa Subcutaneous Injection for Multiple Myeloma
- New Drug Approval: French pharmaceutical giant Sanofi announced that its Sarclisa (isatuximab) subcutaneous formulation has been approved in Japan for multiple myeloma patients, marking a significant advancement in the oncology sector.
- Expanded Indications: The approval for Sarclisa SC includes its use in combination with approved standard treatment regimens, such as with pomalidomide and dexamethasone for relapsed or refractory multiple myeloma, and with bortezomib, lenalidomide, and dexamethasone for newly diagnosed patients, showcasing its broad clinical application potential.
- Clinical Research Support: This approval is based on results from the IRAKLIA phase 3 study, which demonstrated non-inferiority of Sarclisa SC compared to intravenous administration in treating relapsed or refractory multiple myeloma, further enhancing its market competitiveness.
- Innovative Delivery Method: Sanofi's CirCLIQ on-body injector (OBI) is currently under review in Japan, and if approved, Sarclisa SC will become the first anticancer treatment administered via an OBI, significantly improving patient convenience and adherence to treatment.
See More
Denali Sells Rare Pediatric Disease Priority Review Voucher for $195 Million
- Significant Transaction: Denali Therapeutics announced the sale of its Rare Pediatric Disease Priority Review Voucher (PRV) for $195 million, providing a substantial non-dilutive capital infusion that significantly strengthens its financial position.
- Product Background: The PRV was granted following the FDA's accelerated approval of Avlayah (tividenofusp alfa-eknm) in March 2026 for treating Hunter syndrome, highlighting the drug's market potential and the company's competitiveness in the rare disease sector.
- Advancing Clinical Portfolio: The capital infusion will aid Denali in advancing its broad Transport Vehicle-enabled clinical portfolio focused on lysosomal storage disorders and neurodegenerative diseases, further solidifying its position in the biopharmaceutical industry.
- Collaborations and R&D: Denali collaborates with pharmaceutical giants like Sanofi, Biogen, and Takeda to develop various candidates, and despite the discontinuation of the BIIB122 project with Biogen due to unmet expectations, the company will continue to independently advance other key studies, demonstrating resilience and promising prospects in its R&D efforts.
See More
FDA Approves Expanded Use of Sanofi's Diabetes Therapy Tzield
- Indication Expansion: The FDA has approved Sanofi's Tzield therapy for expanded use in stage 3 diabetes patients, aiming to delay insulin production decline in children aged 8 to 17, marking a significant broadening of treatment scope.
- Clinical Trial Support: This approval is backed by data from the PROTECT Phase 3 trial, which demonstrated that patients on Tzield experienced a significant slowdown in C-peptide decline, indicating its effectiveness in delaying diabetes progression.
- Accelerated Approval Pathway: Tzield's accelerated approval allows it to delay the onset of stage 3 diabetes in stage 2 patients, reflecting the FDA's recognition of the therapy's potential benefits, which could lead to greater market opportunities for Sanofi.
- Follow-up Research Plans: Sanofi is currently enrolling patients in the BETA-PRESERVE Phase 3 study, aiming to convert the accelerated approval into standard approval, further solidifying its position in the diabetes treatment landscape.
See More
Sanofi's Tzield Receives FDA Accelerated Approval
- FDA Accelerated Approval: Sanofi's Tzield (teplizumab-mzwv) has received FDA accelerated approval for delaying endogenous insulin production decline in children aged 8 to 17 recently diagnosed with stage 3 type 1 diabetes, marking a significant advancement in diabetes treatment.
- Clinical Research Support: This approval is based on results from the PROTECT phase 3 study and additional data from a global clinical development program involving over 900 patients, demonstrating Tzield's effectiveness in delaying insulin decline, potentially opening new market opportunities for the company.
- Adverse Reaction Concerns: Common adverse reactions associated with Tzield include lymphopenia, vomiting, and rash, with serious events such as cytokine release syndrome and viral reactivation risks, which may affect patient willingness to use the drug and market acceptance.
- Global Regulatory Dynamics: Beyond the U.S., Tzield has also been approved in several countries including the UK, EU, and China, indicating its potential in global markets, while facing ongoing regulatory reviews in other jurisdictions that could impact future sales growth.
See More
Dianthus Therapeutics Receives Strong Buy Rating Following Positive Trial Results
- Clinical Trial Success: Dianthus Therapeutics reported that 75% of patients in its trial for claseprubart, aimed at chronic inflammatory demyelinating polyneuropathy (CIDP), showed significant improvement, exceeding the company's expectation of 50%, thereby enhancing its competitive position in the market.
- Positive Market Reaction: Following the announcement of favorable clinical data, Dianthus's stock surged 8% on Friday, marking its best performance since March, indicating strong investor confidence in its future potential.
- Analyst Rating Maintained: Investment bank Raymond James reaffirmed its 'Strong Buy' rating on Dianthus, keeping the price target at $125 per share, reflecting a positive market outlook, especially in comparison to competing drugs from Sanofi.
- Future Guidance: Dianthus expects to provide guidance on the timing of Part B top-line results by the end of 2026, further increasing investor interest in its research progress, particularly in the treatment of CIDP and other neurological disorders.
See More
Biotech Sector Sees Surge in FDA and Global Approvals
- FDA Approval Boosts Innovation: Guardant Health (GH) secured FDA approval for its Guardant360 CDx liquid biopsy test as a companion diagnostic for Boehringer Ingelheim's HERNEXEOS, highlighting the growing importance of liquid biopsy in advanced cancer treatment, which is expected to drive GH's market share growth.
- Therapy Expansion: Eli Lilly (LLY) received FDA approval for an every-eight-week maintenance dose of EBGLYSS, with Q1 2026 sales surging 141% to $145 million, reflecting strong demand in its immunology portfolio and further solidifying the company's market position.
- China Market Breakthrough: Vor Bio (VOR) announced that Telitacicept received approval from China's NMPA, becoming the only approved therapy for Sjögren's disease in the country, supported by positive Phase 3 trial data, which is expected to significantly improve patient quality of life and expand market reach.
- EU Approval for New Therapy: Sanofi (SNY) secured European Commission approval for Sarclisa in newly diagnosed multiple myeloma patients, based on Phase 3 IRAKLIA trial results, which is expected to enhance Sarclisa's application range and strengthen the company's competitiveness in blood cancer treatment.
See More
