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Century Therapeutics Inc

Century Therapeutics, Inc. is a biotechnology company that develops allogeneic cell therapies for solid tumors, hematological malignancies, and autoimmune diseases. Its lead product candidate is CNTY-813, an iPSC-derived beta islet cell replacement therapy engineered with Allo-Evasion 5.0 for type 1 diabetes. The company is also developing CNTY-308, a CD19-targeted CD4+/CD8+ CAR-iT cell therapy with Allo-Evasion 5.0 for B-cell-mediated autoimmune diseases, and CNTY-101, an allogeneic iPSC-derived CAR-iNK cell therapy with six precision gene edits and Allo-Evasion 1.0 edits targeting CD19 for B-cell-mediated autoimmune diseases. Incorporated in 2018, Century Therapeutics is headquartered in Philadelphia, Pennsylvania.

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Century Therapeutics Q2 GAAP EPS misses estimates by $0.05

Century Therapeutics reported second-quarter 2026 GAAP earnings per share of negative $0.17, missing analyst estimates by $0.05. The company also announced a cash runway extending into the first quarter of 2029, supported by cash, cash equivalents, and investments totaling $197.2 million as of June 30, 2026.
IPSC · Capital · Negative Q2 GAAP EPS missed estimates by $0.05.
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Biotech & Genomic Medicine▲

Century Therapeutics to Present CNTY-813 Data at Two Scientific Congresses

Century Therapeutics announced that its abstracts were accepted for oral presentations at two upcoming scientific congresses, both highlighting CNTY-813, its iPSC-derived islet replacement therapy for type 1 diabetes. The presentations are scheduled for the 62nd Annual Meeting of the European Association for the Study of Diabetes in Milan, Italy, from September 28 to October 2, 2026, and the Breakthrough T1D Clinical & Research Congress 2026 in Philadelphia, Pennsylvania, from October 9 to 11, 2026. CNTY-813 is engineered with Allo-Evasion 5.0 to enable durable engraftment without chronic systemic immunosuppression, and the company is targeting an IND submission in the fourth quarter of 2026. On June 9, Century Therapeutics presented new preclinical data for CNTY-813 at the American Diabetes Association Scientific Sessions, showing durable glucose control for over eight months and maintained insulin secretion under allogeneic immune pressure without immunosuppression. CEO Brent Pfeiffenberger stated the data advance the case for a potentially functional cure for type 1 diabetes, with initial clinical data anticipated in the second half of 2027.
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Biotech & Genomic Medicine › Regenerative Medicine & Tissue Engineering Technology
Biotech & Genomic Medicine › Metabolic, Diabetes & Obesity Technology
IPSC · Technology · Positive Abstracts accepted for oral presentations at two congresses, highlighting CNTY-813's preclinical data showing durable glucose control and insulin secretion without immunosuppression, advancing toward a functional cure for type 1 diabetes.
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Biotech & Genomic Medicine▲

Cutaneous Lupus Erythematosus Market to Grow at 8% CAGR Through 2036, Reaching USD 650 Million in 2025

The cutaneous lupus erythematosus market across the seven major markets was valued at USD 650 million in 2025 and is projected to expand at a compound annual growth rate of 8% during the 2026 to 2036 forecast period, according to a new report from DelveInsight. The United States accounted for the largest share of the market in 2025, representing around 60% of total diagnosed prevalent cases in the seven major markets, which also include the EU4 countries Germany, France, Italy, and Spain, the United Kingdom, and Japan. Antimalarials contributed over 50% of total annual revenue in 2025 across these markets. Growth is being driven by rising autoimmune disease prevalence, improved diagnosis, and a pipeline of emerging targeted therapies such as Litifilimab from Biogen, Daxdilimab from Amgen and Horizon Therapeutics, SOTYKTU from Bristol Myers Squibb, IMVT-1402 from Immunovant Sciences, VENT-03 from Ventus Therapeutics, CNTY-101 from Century Therapeutics, Anifrolumab from AstraZeneca, and Enpatoran from Merck. Biogen's Litifilimab received breakthrough therapy designation from the US FDA in January 2026 and reported positive Phase II results in March 2026, while Amgen announced positive Phase II results for Daxdilimab in discoid lupus erythematosus in 2026 and is considering advancing it to Phase III.
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Biotech & Genomic Medicine › Autoimmune & Immunology Therapeutics ▲Demand
BIIB · Technology · Positive Litifilimab received FDA breakthrough therapy designation and positive Phase II results, driving pipeline optimism.
BIIB · Demand · Positive Biogen's Litifilimab received FDA breakthrough therapy designation and positive Phase II results, positioning it well in the expanding CLE market.
AMGN · Demand · Positive Amgen's Daxdilimab reported positive Phase II results and is advancing to Phase III, indicating strong pipeline progress in a growing market.
BMY · Technology · Positive SOTYKTU is mentioned as an emerging targeted therapy in the pipeline, contributing to market growth.
BMY · Demand · Positive Bristol Myers Squibb's SOTYKTU is mentioned as an emerging therapy in the growing CLE market, benefiting from rising prevalence and diagnosis.
IMVT · Demand · Positive Immunovant's IMVT-1402 is listed as an emerging targeted therapy in the expanding CLE market.
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