Jilin University

SAN FRANCISCO and SUZHOU, China, Aug. 28, 2024 /PRNewswire/ -- Innovent Biologics, Inc. ("Innovent") (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high quality medicines for the treatment of oncology, cardiovascular and metabolic, autoimmune, ophthalmology and other major diseases, announces that nearly 20 accepted clinical data of its novel oncology molecules, including six oral presentations, will be released at World Conference on Lung Cancer (WCLC) from Sept 7-10, 2024, in San Diego, U.S., and the European Society of Medical Oncology (ESMO) from Sept 13-17, 2024, in Barcelona, Spain. Key data showcase includes: an oral presentation of updated Phase 1 result of its first-in-class PD-1/IL-2 α -bias (IBI363) in NSCLC (up to 3mg/kg dosage) at WCLC, updated Phase 1 results of IBI363 (PD-1/IL-2 α -bias ) combination therapy in colorectal cancer at ESMO, an oral presentation of updated pivotal Phase 2 results of Dupert® (fulzerasib, KRAS G12C inhibitor) in NSCLC at WCLC, an oral presentation of Phase 1 results of IBI354 (HER2 ADC) in HER2+ solid tumors at ESMO, and multiple clinical results of TYVYT® (sintilimab injection). Dr. Hui Zhou, Senior Vice President of Innovent, stated: "We are very pleased to present a robust set of clinical data for our next-generation innovative bispecific antibodies and ADC molecules across renowned medical conferences of 2024 including ASCO, ESMO Plenary and ESMO GI in June, and WCLC and ESMO in September. We observed the preliminary efficacy and safety signals for those innovative candidates, underscoring their potential for further development and clinical value. As one of the few biopharmaceutical companies with both the technology platforms and robust pipeline in "IO+ADC" areas, Innovent remains dedicated to advancing cancer treatment and is committed to offering doctors and patients more innovative, effective, and safe therapeutic options." Details on the abstracts are listed below: WCLC: Oral Sessions Abstract Title: First-in-Class PD-1/IL-2 Bispecific Antibody IBI363 In Patients with Advanced Non-Small Cell Lung Cancer in a Phase 1 Study Abstract No: MA11.04 Session Type and Title: WCLC 2024-MA11. Building on the Foundations of Current Immunotherapies Presentation Time: Tuesday, September 10, 2024, 13:37-13:42 PDT Presenter: Jianya Zhou,The First Affiliated Hospital of Zhejiang University School of Medicine Abstract Title: KRAS G12C Inhibitor IBI351 In Patients (pts) with Advanced Non-Small Cell Lung Cancer (NSCLC): Updated Results from a Pivotal Phase 2 Study Abstract No: OA14.05 Session Type and Title: WCLC 2024-OA14. New Horizons in Targeting KRAS G12C Presentation Time: Monday, September 9, 2024, 15:52-16:02 PDT Presenter: Qing Zhou, Guangdong People's Hospital Abstract Title: Neoadjuvant Sintilimab plus Chemotherapy in EGFR-mutant NSCLC Followed by adjuvant Osimertinib or Observation: A Phase 2 CTONG2104 Trial Abstract No: MA15.11 Session Type and Title: Mini Oral Presentation Time: Tuesday, September 10, 2024 at 3:48-3:53 PM PDT Presenter: Guangdong Lung Cancer Institute, C. Zhang Abstract Title: First-Line Treatment of Locally Advanced or Metastatic Pulmonary Lymphoepithelioma-like carcinoma: A Multicenter, Single-Arm, Phase 2 Trial Abstract No: MA11.03 Session Type and Title: Mini Oral Presentation Time: Tuesday, September 10, 2024 at 1:32-1:37 PM PDT Presenter: The First Affiliated Hospital of Medical University, C. Zhou ESMO: Oral Sessions Abstract Title: IBI354 (anti-HER2 antibody-drug conjugate [ADC]) in patients (pts) with advanced solid tumors and breast cancer (BC): results from a Phase 1 study Abstract No: 345MO Session Type and Title: ESMO 2024-Mini oral session 1: Breast cancer, metastatic Presentation Time: Sunday, September 15, 2024, 9:15-9:20 AM CEST Presenter: Christina Teng, Scientia Clinical Research, Australia Abstract Title: IBI354 (anti-HER2 antibody-drug conjugate [ADC]) in patients (pts) with advanced gynecological cancers (Gynecol C): results from a phase 1 study Abstract No: 720MO Session Type and Title: ESMO 2024-Mini oral session 2: Gynecological cancers Presentation Time: Sunday, September 15, 2024, 15:45-15:50 CEST Presenter: Jin Shu, Chongqing University Affiliated Cancer Hospital WCLC: Posters Abstract Title: Neoadjuvant Chemoimmunotherapy for Potentially Resectable IIIA/IIIB NSCLC: Survival Updates and Predictive Effect of MRD Abstract No: EP.08D.01 Session Type and Title: E-Poster Presentation Time: Saturday, September 7, 2024 at 11:58-11:59 AM PDT Presenter: First Hospital of Jilin University, K. Ma Abstract Title: Safety and Efficacy of Sintilimab Combined with Anlotinib in Patients with KRAS-Mutant Advanced Non-Small Cell Lung Cancer Abstract No.: P4.11E.10 Session Type and Title: E-Poster Presentation Time: Monday, September 9, 2024 at 6:30 PM PDT Presenter: Peking University Shenzhen Hospital, F. Wang ESMO: Posters Abstract Title: First-in-class PD-1/IL-2 bispecific antibody fusion protein IBI363 + bevacizumab (beva) in patients (pts) with advanced colorectal cancer (CRC): A phase I study Abstract No: 574P Session Type and Title: ESMO 2024-Poster Presentation Time: Monday, September 16, 2024 CEST Presenter: Zhen Yu Lin, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Abstract Title: Safety and efficacy of IBI354 (anti-HER2 ADC) in patients (pts) with advanced gastrointestinal (GI) cancers: results from a Phase 1 study Abstract No: 576P Session Type and Title: ESMO 2024-Poster Presentation Time: Monday, September 16, 2024 CEST Presenter: Jifang Gong, Peking University Cancer Hospital Abstract Title: Hepatic Artery Infusion Chemotherapy (HAIC) Plus Sintilimab and Bevacizumab Biosimilar (IBI305) for Initial Unresectable Hepatocellular Carcinoma (HCC) in Patients with Child-Pugh B Liver Function: A prospective study Abstract No.: 980P Session Type and Title: Hepatocellular carcinoma (HCC) - Poster Presentation Time: Monday, September 16, 2024 Presenter: Tianjin Medical University Cancer Institute & Hospital, Huikai Li Abstract Title: Hepatic arterial infusion chemotherapy combined with Sintilimab and regorafenib as adjuvant therapy for colorectal liver metastasis patients with high risk of recurrent: a single-arm, Phase 2 study Abstract No.: 539P Session Type and Title: Colorectal cancer - Poster Presentation Time: Monday, September 16, 2024 Presenter: Fudan University Shanghai Cancer Center, Lu Wang Abstract Title: Fruquintinib combined with sintilimab and chemotherapy as the first-line treatment in advanced naïve EGFR- and ALK-negative non-squamous non-small cell lung cancer (nsq-NSCLC): Updated results Abstract No: 1329P Session Type and Title: NSCLC, metastatic - Poster Presentation Time: Saturday, September 14, 2024 Presenter: Jiangsu Province Hospital, Pei Ma Abstract Title: Sintilimab plus anlotinib in patients with advanced sarcomas (SINANLOSARC): a single-center, single-arm, Phase 2 trial Abstract No.: 1735P Session Type and Title: Sarcoma - Poster Presentation Time: Saturday, September 14, 2024 Presenter: Shandong Cancer Institute, Shandong Cancer Hospital, Zengjun Liu Abstract Title: Efficacy and safety of sintilimab in combination with anlotinib plus metronomic chemotherapy in advanced triple negative breast cancer (SPACE): preliminary results of a single-arm, multicenter Phase 2 trial Abstract No.: 389P Session Type and Title: Breast cancer, metastatic - Poster Presentation Time: Monday, September 16, 2024 Presenter: Shandong Cancer Institute, Shandong Cancer Hospital, Huihui Li Trial in Progress Abstract Title: Fruquintinib in combination with sintilimab and CAPEOX as first-line treatment for advanced G/GEJ cancer: A phase 1b/2 clinical trial (FUNCTION) Abstract No.: 1475TiP Session Type and Title: Oesophagogastric cancer, Poster Presentation Time: Monday, September 16, 2024 Presenter: Henan Cancer Hospital, Bei-Bei Chen About Innovent Innovent is a leading biopharmaceutical company founded in 2011 with the mission to empower patients worldwide with affordable, high-quality biopharmaceuticals. The company discovers, develops, manufactures and commercializes innovative medicines that treat some of the most intractable diseases. Its pioneering therapies treat cancer, cardiovascular and metabolic, autoimmune and eye diseases. Innovent has 11 products in the market, 3 new drug applications under the NMPA review, 4 assets in Phase III or pivotal clinical trials and 18 more molecules in early clinical stage. Innovent partners with over 30 global healthcare leaders, including Eli Lilly, Roche, Sanofi, Adimab, Incyte and MD Anderson Cancer Center. Guided by the motto, "Start with Integrity, Succeed through Action," Innovent maintains the highest standard of industry practices and works collaboratively to advance the biopharmaceutical industry so that first-rate pharmaceutical drugs can become widely accessible. For more information, visit , or follow Innovent on Facebook and LinkedIn. Forward-looking statement This news release may contain certain forward-looking statements that are, by their nature, subject to significant risks and uncertainties. The words "anticipate", "believe", "estimate", "expect", "intend" and similar expressions, as they relate to Innovent Biologics ("Innovent"), are intended to identify certain of such forward-looking statements. The Company does not intend to update these forward-looking statements regularly. These forward-looking statements are based on the existing beliefs, assumptions, expectations, estimates, projections and understandings of the management of the Company with respect to future events at the time these statements are made. These statements are not a guarantee of future developments and are subject to risks, uncertainties and other factors, some of which are beyond the Company's control and are difficult to predict. Consequently, actual results may differ materially from information contained in the forward-looking statements as a result of future changes or developments in our business, the Company's competitive environment and political, economic, legal and social conditions. The Company, the Directors and the employees of the Company assume (a) no obligation to correct or update the forward-looking statements contained in this site; and (b) no liability in the event that any of the forward-looking statements does not materialise or turn out to be incorrect. SOURCE Innovent Biologics

WEDNESDAY, Aug. 14, 2024 -- Gastroesophageal reflux disease (GERD) increases the risk for rheumatoid arthritis (RA), according to a study published online Aug. 1 in Scientific Reports . Quan Yuan, from the First Hospital of Jilin University in Changchun, China, and colleagues used Mendelian randomization (MR) to assess the causal relationship between GERD and RA. The researchers found that MR results suggest a causal effect of the genetic susceptibility of GERD on RA (discovery dataset, inverse variance weighting, odds ratio, 1.41; validation dataset, inverse variance weighting, odds ratio, 1.38). When adjusting for confounding factors between GERD and RA, including smoking quantity, drinking frequency, body mass index, depression, and education attainment, MR analysis results were similar. However, the reverse MR analysis did not show evidence that RA can increase the risk for developing GERD. "This finding is crucial for deepening our understanding of the pathogenesis of RA and may offer new insights for the prevention and treatment of RA," the authors write. "It also offers a new perspective on preventing the occurrence of GERD in patients with RA. However, based on the results of the reverse MR analysis using the existing dataset, compelling evidence was not found for RA increasing the risk of developing GERD." Abstract/Full Text Whatever your topic of interest, subscribe to our newsletters to get the best of Drugs.com in your inbox.

– The company to present important new data from two Phase I trials of its leading molecule, AHB-137, aimed at achieving a functional cure for chronic hepatitis B, in two late-breaker posters.SAN FRANCISCO, May 28, 2024 /PRNewswire/ -- AusperBio Therapeutic s , Inc. and Ausper Biopharma Co., Ltd. (together AusperBio), a clinical-stage biotechnology company, today announced the clinical data of the Company's HBV ASO molecule, AHB-137, will be presented in two late-breaking posters, LBP-019 and LBP-043, at the annual European Association for the Study of the Liver (EASL™) Congress 2024, to be held in Milan, Italy, from June 5th to 8th, 2024. These posters will highlight new data from two Phase I clinical studies conducted both globally and in China, evaluating the safety, tolerability, pharmacokinetics, and preliminary efficacy of AHB-137. Continue Reading Poster presentation details are as follows: EASL 2024, AHB-137, Chronic Hepatitis B, Functional Cure, ASO Post this Title: Safety and antiviral activity of AHB-137, a novel antisense oligonucleotide, in healthy volunteers and subjects with chronic hepatitis B (Abstract # LB249; Poster# LBP-019) Session: Late breaker posters Date: Wednesday, June 5, 2024 Time: Available from 8:30 a.m. CEST Presenter: Prof. Edward J. Gane, University of Auckland, New Zealand Title: A phase 1, dose-escalation and dose-expansion study evaluating the safety, tolerability, pharmacokinetics and preliminary efficacy of AHB-137 in Chinese healthy volunteers and subjects with chronic hepatitis B (Abstract# LB256; Poster# LBP-043) Session: Late breaker posters Date: Wednesday, June 5, 2024 Time: Available from 8:30 a.m. CEST Presenter: Wen Wang, The First Hospital of Jilin University, ChinaThe full scientific program for The International Liver Congress 2024, as well as the abstracts, can be found at . About AHB-137AHB-137, a novel unconjugated antisense oligonucleotide ( ASO) developed within AusperBio's proprietary Med-Oligo™ ASO technology platform, is emerging as a promising candidate in the quest for a functional cure for chronic hepatitis B. Its compelling preclinical data was highlighted at the 2023 EASL™ conference. This novel dual-mechanism ASO is currently undergoing concurrent Phase I trials across international multicenter sites and a Phase I/IIa trial in China. Through the global development strategy, AHB-137 is advancing rapidly towards the goal of a functional cure for chronic hepatitis B. About Chronic Hepatitis BChronic Hepatitis B (CHB) infection is a liver disease estimated to affect nearly 290 million people worldwide and can cause other chronic complications such as cirrhosis and hepatocellular carcinoma. Although current treatment options can suppress HBV replication, achieving a cure is rare. Therefore, the discovery of a cure for CHB with finite treatment is an urgent need. About AusperBio. AusperBio is a clinical-stage biopharmaceutical company with operations in the USA and China, dedicated to advancing oligonucleotide and targeted delivery technologies for transformative therapies, with an initial focus on curing chronic hepatitis B. The company has developed a proprietary Med-Oligo™ ASO platform with novel insights into ASO design and capabilities to substantially enhance the current ASO therapeutics. Combining with efficient targeted delivery conjugation technologies, the modular Med-Oligos™ Platform empowers ASO therapeutics to treat broad viral infections, metabolic conditions, genetic disorders, and immune diseases. For more information, visit Media Contact Email: [email protected] Investor Contact Tel: 650-888-1756 (US) Email: [email protected] SOURCE AusperBio Therapeutics Inc.