A new inhalable gene therapy for cystic fibrosis (CF) has entered Phase I clinical trials, a major milestone on the journey ...
An inhalable medicine with the potential to improve lung disease in people with cystic fibrosis, irrespective of their mutation type.
An inhaled gene therapy for cystic fibrosis developed by Boehringer Ingelheim is due to start clinical testing shortly, hoping to become a first-in-class treatment for the genetic disorder.
Boehringer Ingelheim, IP Group, the UK Respiratory Gene Therapy Consortium (GTC) 1 and OXB, 1 today announce the start of LENTICLAIR TM 1, a Phase I/II trial of BI 3720931, a novel, first-in-class, ...
"Boehringer and partners commence gene therapy trial for cystic fibrosis" was originally created and published by Clinical Trials Arena, a GlobalData owned brand.
OXB announces that its proprietary lentiviral vector manufacturing technology will be used in Boehringer Ingelheim’s newly initiated LENTICLAIR ...
An inhalable medicine with the potential to improve lung disease in people with cystic fibrosis, irrespective of their ...
An inhalable medicine with the potential to improve lung disease in people with cystic fibrosis is being tested in human ...
Cystic fibrosis (CF) is caused by defects in the ... The new lentiviral vector-based gene therapy works by inserting a functioning copy of the CFTR gene in the DNA of the epithelial cells in ...
An inhalable medicine with the potential to improve lung disease in people with cystic fibrosis, irrespective of their mutation type, is being tested in human trials in the UK and Europe.