- |||||||||| eribulin liposome (HR19024) / Jiangsu Hengrui Pharma
Trial completion, Phase classification, Enrollment change, Trial completion date, Trial primary completion date: A Study of HR19024 in Subjects With Advanced Solid Tumor (clinicaltrials.gov) - Mar 20, 2025 P1, N=71, Completed, However, pyrotinib plus trastuzumab did not show better efficacy compared with Per Recruiting --> Completed | Phase classification: P1a --> P1 | N=180 --> 71 | Trial completion date: Jul 2023 --> Oct 2024 | Trial primary completion date: Jul 2023 --> Oct 2024
- |||||||||| HRS-1780 / Jiangsu Hengrui Pharma, Ruiqin (henagliflozin) / Jiangsu Hengrui Pharma
Enrollment closed, Trial primary completion date: Efficacy and Safety of HRS-1780 Tablets and Henagliflozin Proline Tablets in Patients With Chronic Kidney Disease (clinicaltrials.gov) - Mar 20, 2025 P2, N=181, Active, not recruiting, Recruiting --> Completed | Phase classification: P1a --> P1 | N=180 --> 71 | Trial completion date: Jul 2023 --> Oct 2024 | Trial primary completion date: Jul 2023 --> Oct 2024 Recruiting --> Active, not recruiting | Trial primary completion date: Dec 2024 --> Mar 2025
- |||||||||| Enrollment open: A Trial of SHR0302Base in Patients With Vitiligo (clinicaltrials.gov) - Mar 19, 2025
P2, N=152, Recruiting, Lenvatinib/bevacizumab combined with programmed death-1 (PD-1)/programmed death ligand 1 (PD-L1) inhibitors and gemcitabine/oxaliplatin (GEMOX) represent an effective and tolerable regimen for advanced BTC in a multicenter retrospective real-world study. Not yet recruiting --> Recruiting
- |||||||||| AiRuiKa (camrelizumab) / HLB Bio Group, Lenvima (lenvatinib) / Eisai, Merck (MSD)
Journal, PD(L)-1 Biomarker, IO biomarker: Clinical efficacy and safety of transarterial chemoembolization combined with targeted therapy and PD1 inhibitors in patients with advanced liver cancer. (Pubmed Central) - Mar 19, 2025 The overall response rate(ORR) was 80% in the experimental group and 62% in the control group, and the difference was statistically significant(p=0.03); the incidence of adverse reactions was 28% in the experimental group and 25% in the control group, with no significant difference between the two groups(p=0.68); the improvement rate of QOL score was significantly increased(p=0.03) and the deterioration rate was significantly decreased(p=0.01) in the experimental group compared with those in the control group, respectively. TACE combined with targeted therapy and PD1 inhibitors is significantly effective to improve the cellular immune function with no significant increase in the incidence of adverse reactions, making it an effective and safe treatment option for patients with liver cancer.
- |||||||||| carfilzomib / Generic mfg., HRS-4642 / Jiangsu Hengrui Pharma
Journal: New exploration of KRASG12D inhibitors and the mechanisms of resistance. (Pubmed Central) - Mar 18, 2025 Here, we aim to describe a potential novel therapy for patients with KRASG12D mutations and present the first KRASG12D-specific inhibitor to be proven as clinically effective. Different mutations of KRAS gene and mechanisms of KRAS drug resistance were also discussed.
- |||||||||| AiRuiKa (camrelizumab) / Elevar Therapeutics
Trial completion date, Trial initiation date, Trial primary completion date: A Trial of Camrelizumab Plus Nab-paclitaxel and Levocetirizine in Metastatic or Recurrent TNBC (clinicaltrials.gov) - Mar 17, 2025 P2, N=60, Not yet recruiting, Trial primary completion date: Dec 2024 --> Jun 2025 Trial completion date: Dec 2026 --> Mar 2027 | Initiation date: Oct 2024 --> Apr 2025 | Trial primary completion date: Dec 2026 --> Mar 2027
- |||||||||| paclitaxel / Generic mfg., AiRuiKa (camrelizumab) / HLB Bio Group
Journal, Checkpoint inhibition: Dermatitis bullosa caused by the immune checkpoint inhibitor camrelizumab: A case report. (Pubmed Central) - Mar 17, 2025 Early recognition and accurate diagnosis, combined with interdisciplinary collaboration and swift initiation of immunosuppressive therapy, are essential in managing severe immune-related adverse reactions effectively. This report details the treatment trajectory and outcome of a case involving immune-related cutaneous adverse reactions, providing pertinent clinical insights for future cases.
- |||||||||| ByFavo (remimazolam) / PAION, Cosmo Pharma, Mundipharma, Pharmascience, Eagle Pharma, remimazolam tosylate (HR-7056) / Jiangsu Hengrui Pharma
Clinical, Retrospective data, Journal: Comparison of remimazolam tosylate and propofol in hemodynamic stability, postoperative cognitive function, and recovery in general anesthesia combined with regional nerve blocks: a retrospective cohort study. (Pubmed Central) - Mar 16, 2025 However, insufficient dosing of pyrotinib may impair efficacy outcomes. Remimazolam tosylate was associated with more stable hemodynamic parameters, lower rates of postoperative cognitive dysfunction, and shorter recovery times compared to propofol in patients undergoing GA combined with RA, suggesting it may be a safer alternative for patients.
- |||||||||| Varubi (rolapitant oral) / TerSera Therap, GSK, HR20013 / Jiangsu Hengrui Pharma, Varubi IV (rolapitant IV) / TerSera Therap, GSK
P3 data, Journal, CINV: Randomized, Phase III Trial of Mixed Formulation of Fosrolapitant and Palonosetron (HR20013) in Preventing Cisplatin-Based Highly Emetogenic Chemotherapy-Induced Nausea and Vomiting: PROFIT. (Pubmed Central) - Mar 14, 2025 Remimazolam tosylate was associated with more stable hemodynamic parameters, lower rates of postoperative cognitive dysfunction, and shorter recovery times compared to propofol in patients undergoing GA combined with RA, suggesting it may be a safer alternative for patients. HR20013 + DEX was noninferior to FAPR + PALO + DEX for preventing HEC-CINV and well tolerated, with the potential to reduce the impact of CINV on daily life.
- |||||||||| Retrospective data, Journal, PD(L)-1 Biomarker, IO biomarker: Comparison of camrelizumab, pembrolizumab, tislelizumab, and sintilimab as first-line treatment in patients with non-small cell lung cancer: a retrospective study. (Pubmed Central) - Mar 14, 2025
Camrelizumab, pembrolizumab, tislelizumab, and sintilimab possess similar efficacy as first-line treatment options for patients with advanced NSCLC in Chinese clinical practice. Any grade or grade ?3 irAEs are comparable between the four PD-1 inhibitors.
- |||||||||| P2 data, Journal, PD(L)-1 Biomarker, IO biomarker: PD-1 antibody camrelizumab plus apatinib and SOX as first-line treatment in patients with AFP-producing gastric or gastro-esophageal junction adenocarcinoma (CAP 06): a multi-center, single-arm, phase 2 trial. (Pubmed Central) - Mar 14, 2025
P2 This multi-center, single-arm, phase 2 trial (ClinicalTrials.gov NCT04609176) evaluated the antitumor activity, safety, and biomarkers of camrelizumab plus apatinib and S-1 and oxaliplatin (SOX), followed by maintenance treatment with camrelizumab plus apatinib, as a first-line treatment in patients with AFP-G/GEJ adenocarcinoma...First-line treatment with camrelizumab plus apatinib and SOX, followed by maintenance treatment with camrelizumab plus apatinib, is effective and safe in AFP-G/GEJ adenocarcinoma. Further studies are necessary to validate these findings.
- |||||||||| AiTan (rivoceranib) / HLB Bio Group
Journal: Cocry-pred: A Dynamic Resource Propagation Method for Cocrystal Prediction. (Pubmed Central) - Mar 12, 2025 Subsequently, seven Apatinib cocrystals were then synthesized experimentally, among which single-crystal structures were obtained for two cocrystals. This advancement highlights the potential of Cocry-pred as a powerful tool, offering significant improvements in efficiency and providing valuable insights for cocrystal screening and design.
- |||||||||| Ruiqin (henagliflozin) / Jiangsu Hengrui Pharma
Trial completion, Trial completion date, Trial primary completion date: Combination of Henagliflozin and Continuous Subcutaneous Insulin Infusion in T2DM (clinicaltrials.gov) - Mar 12, 2025 P4, N=210, Completed, Recruiting --> Completed | Trial completion date: Aug 2022 --> Jul 2024 | Trial primary completion date: Aug 2021 --> Jul 2024 Recruiting --> Completed | Trial completion date: Aug 2024 --> Oct 2024 | Trial primary completion date: Jul 2024 --> Oct 2024
- |||||||||| AiRuiKa (camrelizumab) / HLB Bio Group
Biomarker, PD(L)-1 Biomarker, IO biomarker: Case Report: Complete response to four cycles of camrelizumab in a PD-L1 negative patient with advanced oral squamous cancer. (Pubmed Central) - Mar 11, 2025 This situation has not been reported previously, suggesting that some patients can benefit from short-term immunotherapy and even achieve CR; moreover, there may be more molecular markers to be discovered that can predict the efficacy of immunotherapy. We can conduct in-depth research on relevant molecular markers, formulate personalized immunotherapy strategies and plans, and facilitate the development of new precision treatment strategies for HNSCC.
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