Milestone achieved! The first SCD patient treated in China with our high-precision base-editing therapy CS-206 has remained VOC-free for >15 months post-engraftment, achieving the primary efficacy endpoint. No product-related AEs have been observed to date. #SCD#BaseEditing
📢We will give 2 poster presentations at the American Society of Gene & Cell Therapy 2026 Annual Meeting, taking place May 11 – 15, 2026, in Boston, MA and online. 📰Poster #1506, 05/12. 📰Poster #3411, 05/14. @ASGCTherapy#GeneEditing#ASGCT2026
Proud moment for CS-101 🚀
Published in @Nature on April 8, CS-101 enabled β-thal patients to achieve rapid, durable transfusion independence after a single treatment, with strong safety signals.nature.com/articles/s41586-0…
📢We will give a poster presentation at the 67th American Society of Hematology Annual Meeting and Exposition, taking place December 6-9, 2025, in Orlando, Florida, and online.
📄Poster #6090
🗓 Dec 8, 6–8 PM EST
📍OCCC-West Halls B3-B4 #ASH25@ASH_hematology#GeneEditing
📢 Breakthrough in gene editing!
@Correctseq CS-121, targeting APOC3, successfully treated the first chylomicronemia patient — TG levels dropped significantly within 3 days after a single low-dose, with no adverse events. prn.to/496nsWI#GeneEditing#biotech
🚀 WORLD FIRST: Correctseq's CS-121 has completed dosing of first chylomicronemia patient, demonstrating excellent safety and significant efficacy. It's the world’s first gene-editing therapy targeting APOC3 for hyperlipidemia. A major milestone for #GeneEditing#Hyperlipidemia
ALT The world’s first patient of the gene-editing therapy targeting APOC3 (Correctseq’s CS-121) for hyperlipidemia (the 6th from the right) has successfully completed dosing and been discharged.
📢Breakthrough! Our CS-101 base-editing therapy achieved the first clinical cure of sickle cell disease (SCD) in China.
✅Patient showed sustained HbF↑, HbS↓, HbF:HbS=6.5:3.5(the 6th months), Hb>120 g/L.
💪6 months crisis-free & back to normal life.prn.to/4mw2RPd
At #EHA2025 in #Milan this week? Jia Chen, Ph.D., Professor and Director, Gene Editing Center, ShanghaiTech University, Co-founder of Correctseq, will give an oral presentation at 11:00~12:15(CEST), June 15, 2025. @EHA_Hematology
ALT Specific and Efficient RNA A-to-I Editing through Cleavage of an ADAR Inhibitor
ALT Figure 1: Schematic of the RtABE working mechanism
ALT Figure 2: Comparison of editing efficacy between RtABE_V2 and MCP-ADAR2DD systems. (Left) Editing efficiencies induced by RtABE_V2 and MCP-ADAR2DD in mouse liver. (Right) Transcriptome-wide off-target counts induced by RtABE_V2 and MCP-ADAR2DD in mouse liver.
ALT Leveraging base excision repair for efficient adenine base editing of mitochondrial DNA
ALT Figure 1: Schematic of the TALED working mechanism
ALT Figure 2: Editing efficiency (top), product purity (middle), and transcriptome-wide off-target counts (bottom) mediated by sTALED, eTALED6, and eTALED6R at the m.13514 site in the mitochondrial genome
🌏🧬 BREAKING: Our base editing therapy CS-101 hits new milestone in β-thalassemia treatment! Successfully treated 2nd overseas patient - a Malaysian with transfusion-dependent β-thalassemia. 🩸✨ #GeneEditingTherapy#TDT#thalassemia#GlobalHealth
ALT A Malaysian β-thalassemia patient who received base editing therapy (Correctseq’s CS-101) in China has been transfusion-free and returned to normal life.
#Shanghai-based CorrectSequence Therapeutics (#Correctseq) has partnered with the First Affiliated Hospital of #Guangxi Medical University to apply base editing therapy to successfully free a Lao patient suffering from β-thalassemia from dependence on blood transfusions for over 2 months.
It was China’s first successful attempt to use the therapy to cure a foreign patient, which will bring hope to the complete cure of β-hemoglobinopathies patients worldwide. @Correctseq
#Shanghai-based CorrectSequence Therapeutics (#Correctseq) has partnered with the First Affiliated Hospital of #Guangxi Medical University to apply base editing therapy to successfully free a Lao patient suffering from β-thalassemia from dependence on blood transfusions for over 2 months.
It was China’s first successful attempt to use the therapy to cure a foreign patient, which will bring hope to the complete cure of β-hemoglobinopathies patients worldwide. @Correctseq
We are excited to announced a significant milestone in our base editing therapy CS-101. Utilizing our pioneering transformer Base Editor (tBE), we have successfully cured the first overseas patient with transfusion-dependent β-thalassemia in the clinical trial.
Recently, as the world's first base editing therapy for hemoglobinopathies, CS-101 of @Correctseq was included in the EHA2024 Scientific Congress Report for its safe and efficient base editing technology and the promising clinical results.@EHA_Hematology
ALT EHA2024 Scientific Congress Report
ALT Dr. Lijie Wang, Head of Gene Editing Platform of Correctseq, gave an oral presentation at the EHA2024 Hybrid Congress
ALT The editing process of tBE (From EHA2024 Scientific Congress Report)
At #BIO2024 in #SanDiego this week? Susan Mou, Ph.D., Chief Executive Officer of Correctseq, will give an oral presentation titled "Development of Next Generation Gene Editing Therapy Using Innovative Transformer Base Editor (tBE)" .@BIOConvention