LBL-015 / Leads Biolabs 
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  • ||||||||||  LBL-015 / Leads Biolabs
    Trial completion, Enrollment change, Trial completion date, Trial primary completion date:  Phase I/II Clinical Trial of LBL-015 for Injection (clinicaltrials.gov) -  Oct 28, 2024   
    P1/2,  N=25, Completed, 
    Recruiting --> Completed | N=202 --> 25 | Trial completion date: Dec 2024 --> Dec 2023 | Trial primary completion date: Oct 2024 --> Dec 2023
  • ||||||||||  LBL-015 / Leads Biolabs
    Trial primary completion date, Metastases:  Phase I/II Clinical Trial of LBL-015 for Injection (clinicaltrials.gov) -  Nov 9, 2023   
    P1/2,  N=202, Recruiting, 
    signaling pathway deregulated or activated tumors such as RCC, pancreatic cancer, etc. should be further explored. Trial primary completion date: Oct 2023 --> Oct 2024
  • ||||||||||  LBL-015 / Leads Biolabs
    Enrollment open, Metastases:  Phase I/II Clinical Trial of LBL-015 for Injection (clinicaltrials.gov) -  Dec 10, 2021   
    P1/2,  N=202, Recruiting, 
    Trial primary completion date: Oct 2023 --> Oct 2024 Not yet recruiting --> Recruiting
  • ||||||||||  LBL-015 / Leads Biolabs
    [VIRTUAL] LBL-015, a novel anti-PD-1 fused with TGF-βRII, shows a great anti-tumor activity in a mouse MC38 model () -  Mar 11, 2021 - Abstract #AACR2021AACR_2983;    
    In vitro LBL-015 could block PD-1-PD-L1 interaction, recovering NFAT reporter gene signal, with EC50 of 0.1565 nM, which was much more potent than M7824 (EC50 of 0.5412 nM). LBL-015, an anti-PD-1 and TGF-β bispecific fusion protein was shown a great synergetic anti-tumor efficacy in vitro to antagonize both tumor immune evasion and aberrant microenvironment induced by PD-1 and TGF-β1, also in a mouse tumor model, LBL-015 strongly inhibited tumor growth in a dose dependent manner, hence a promising bispecific fusion protein for further clinical development.