Jiangsu Hengrui Pharma 
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  • ||||||||||  AiTan (rivoceranib) / HLB Bio Group, AiRuiKa (camrelizumab) / HLB Bio Group
    Trial completion date, Trial primary completion date:  FZPL-Ib-105: A Trial of SHR-1210 (an Anti-PD-1 Inhibitor) in Combination With Apatinib and Fluzoparib in Patients With TNBC (clinicaltrials.gov) -  Mar 19, 2020   
    P1,  N=52, Recruiting, 
    Fluzoparib had demonstrated promising antitumor activity and an acceptable safety profile in patients with recurrent BRCA1- or BRCA2-mutated ovarian cancer. Trial completion date: Dec 2020 --> Aug 2021 | Trial primary completion date: Dec 2019 --> Apr 2021
  • ||||||||||  AiTan (rivoceranib) / HLB Bio Group, AiRuiKa (camrelizumab) / HLB Bio Group
    Enrollment change, Trial primary completion date, PD(L)-1 Biomarker, IO biomarker:  A Trial of SHR-1210 (an Anti-PD-1 Antibody) in Combination With Apatinib in Patients With Advanced TNBC (clinicaltrials.gov) -  Mar 17, 2020   
    P2,  N=40, Active, not recruiting, 
    Phase classification: P2/3 --> P3 N=58 --> 40 | Trial primary completion date: Jun 2020 --> Aug 2019
  • ||||||||||  AiRuiKang (dalpiciclib) / Jiangsu Hengrui Pharma
    Enrollment open:  A Trial of SHR6390 in Healthy Caucasian Volunteers (clinicaltrials.gov) -  Mar 16, 2020   
    P1,  N=36, Recruiting, 
    N=58 --> 40 | Trial primary completion date: Jun 2020 --> Aug 2019 Not yet recruiting --> Recruiting
  • ||||||||||  AiTan (rivoceranib) / HLB Bio Group
    Clinical, Journal:  Efficacy and Safety of Apatinib in the Treatment of Postoperative Recurrence of Fibrosarcoma. (Pubmed Central) -  Mar 13, 2020   
    Apatinib is a single-drug regimen that can be used in cases of recurrence of fibrosarcoma with high expression of vascular endothelial growth factor receptor-2 (VEGFR-2); its short-term efficacy is excellent, and its side effects are minimal. This drug may be used as part of a regular chemotherapy program.
  • ||||||||||  AiTan (rivoceranib) / HLB Bio Group
    Journal:  Quantification of the plasma concentration of apatinib by two-dimensional liquid chromatography (2D-LC). (Pubmed Central) -  Mar 12, 2020   
    We plan to conduct randomized clinical trials to confirm and characterize the activity of the chemotherapy-immunotherapy combinations in the treatment of sarcomas. A simple, convenient, accurate and robust two-dimensional liquid chromatography method was developed and verified, which successfully determined the plasma concentrations of apatinib in gastric cancer patients.
  • ||||||||||  plinabulin (BPI 2358) / BeyondSpring
    Trial completion date, Trial primary completion date:  DUBLIN-3: Docetaxel + Plinabulin Compared to Docetaxel + Placebo in Patients With Advanced NSCLC (clinicaltrials.gov) -  Mar 11, 2020   
    P3,  N=554, Recruiting, 
    A simple, convenient, accurate and robust two-dimensional liquid chromatography method was developed and verified, which successfully determined the plasma concentrations of apatinib in gastric cancer patients. Trial completion date: Mar 2020 --> Jun 2020 | Trial primary completion date: Feb 2020 --> May 2020
  • ||||||||||  perfluorohexyloctane (NOV03) / Novaliq, Bausch Health
    Effects of Perfluorohexyloctane on Signs and Symptoms of Dry Eye Disease: SEECASE-1: Subgroup Analysis based on Baseline Characteristics (Exhibit Hall: Posterboard# A0151) -  Mar 9, 2020 - Abstract #ARVO2020ARVO_602;    
    P2
    The same pattern was seen for CFB inDryness score for subjects with baseline MGD score ≥ 7 (point estimate of -13.39; p≤0.01) andSchirmer I test ≥ 10 (point estimate -19.96; p≤0.001)Conclusions Treatment with NOV03 QID significantly reduced corneal staining and severity of dryness in all subjects with DED compared to control. The improvements were greater in subjects with more pronounced evaporative DED characterized by higher MGD and Schirmer I test scores at baseline.
  • ||||||||||  imrecoxib (BAP 909) / Jiangsu Hengrui Medicine, celecoxib oral / Generic mfg.
    [VIRTUAL] COST-EFFECTIVENESS ANALYSIS OF IMRECOXIB, CELECOXIB AND DICLOFENAC IN OSTEOARTHRITIS IN CHINA () -  Mar 8, 2020 - Abstract #ISPOR2020ISPOR_1909;    
    In Chinese OA patients aged ≥65 years, the ICER was $3856 and $2738 for imrecoxib versus celecoxib and diclofenac, respectively, over a 6-month treatment duration. CONCLUSIONS With the gross domestic product/capita in Chinese in 2018 was $10407, the imrecoxib can be a cost-effective option over different treatment durations in Chinese OA patients.
  • ||||||||||  AiTan (rivoceranib) / HLB Bio Group
    Trial completion, Enrollment change, Trial completion date, Metastases:  Apatinib for Advanced Soft Tissue Sarcoma Patients: a Phase 2, Multicenter Trial (clinicaltrials.gov) -  Mar 6, 2020   
    P2,  N=30, Completed, 
    No abstract available Suspended --> Completed | N=100 --> 30 | Trial completion date: Jun 2021 --> Mar 2020
  • ||||||||||  AiTan (rivoceranib) / HLB Bio Group
    New P3 trial, BRCA Biomarker, PARP Biomarker:  FABULOUS: A Study of Fluzoparib (clinicaltrials.gov) -  Mar 5, 2020   
    P3,  N=474, Not yet recruiting, 
  • ||||||||||  AiTan (rivoceranib) / HLB Bio Group
    Retrospective data, Journal:  Apatinib for chemotherapy-refractory extensive-stage SCLC: a retrospective study. (Pubmed Central) -  Mar 4, 2020   
    Therefore, we suggested that MBRI-001 could be developed as a promising anti-cancer agent in near future. Apatinib exhibits modest activity and acceptable toxicity for patients with heavily pretreated extensive-stage SCLC.
  • ||||||||||  AiTan (rivoceranib) / HLB Bio Group
    Journal:  Apatinib for hepatocellular carcinoma. (Pubmed Central) -  Mar 3, 2020   
    Active, not recruiting --> Recruiting No abstract available