TY - JOUR
T1 - Therapeutic targets and early stage clinical trials for pulmonary fibrosis
AU - Sato, Seidai
AU - Yanagihara, Toyoshi
AU - Kolb, Martin R.J.
N1 - Publisher Copyright:
© 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2019/1/2
Y1 - 2019/1/2
N2 - Introduction: Idiopathic pulmonary fibrosis (IPF) is an age-associated, progressive, and irreversible fatal interstitial lung disease. Although many drugs have failed in clinical trials, these failures improved the understanding of the pathogenesis of IPF. Currently, there are two drugs approved for IPF that slow the progression of the disease. However, the prognosis for patients with IPF remains poor and the search continues for drugs that inhibit the pathogenic pathways active in IPF to further reduce or even halt the progression of the disease. Areas covered: We highlight the recent information on the therapeutic targets currently explored in early stage clinical trials and discuss the potential for new therapy and the limitation of basic research in the treatment of IPF. Expert opinion: A key challenge in the coming years will lie in deciding which compounds to combine and how to evaluate combination therapies in clinical trials. The drugs most likely to provide additive efficacy when used in combination with one of the approved therapies are those with alternative, complementary, or synergistic mechanisms of action. Trial registration:ClinicalTrials.gov identifier: NCT02257177. Trial registration:ClinicalTrials.gov identifier: NCT02738801. Trial registration:ClinicalTrials.gov identifier: NCT02538536. Trial registration:ClinicalTrials.gov identifier: NCT02503657. Trial registration:ClinicalTrials.gov identifier: NCT01371305. Trial registration:ClinicalTrials.gov identifier: NCT02550873. Trial registration:ClinicalTrials.gov identifier: NCT02688647. Trial registration:ClinicalTrials.gov identifier: NCT01872689. Trial registration:ClinicalTrials.gov identifier: NCT01529853. Trial registration:ClinicalTrials.gov identifier: NCT02345070. Trial registration:ClinicalTrials.gov identifier: NCT01629667. Trial registration:ClinicalTrials.gov identifier: NCT01890265. Trial registration:ClinicalTrials.gov identifier: NCT01262001. Trial registration:ClinicalTrials.gov identifier: NCT03142191. Trial registration:ClinicalTrials.gov identifier: NCT02036970. Trial registration:ClinicalTrials.gov identifier: NCT00463983. Trial registration:Japan Primary Registries Network identifier: JapicCTI-183898.
AB - Introduction: Idiopathic pulmonary fibrosis (IPF) is an age-associated, progressive, and irreversible fatal interstitial lung disease. Although many drugs have failed in clinical trials, these failures improved the understanding of the pathogenesis of IPF. Currently, there are two drugs approved for IPF that slow the progression of the disease. However, the prognosis for patients with IPF remains poor and the search continues for drugs that inhibit the pathogenic pathways active in IPF to further reduce or even halt the progression of the disease. Areas covered: We highlight the recent information on the therapeutic targets currently explored in early stage clinical trials and discuss the potential for new therapy and the limitation of basic research in the treatment of IPF. Expert opinion: A key challenge in the coming years will lie in deciding which compounds to combine and how to evaluate combination therapies in clinical trials. The drugs most likely to provide additive efficacy when used in combination with one of the approved therapies are those with alternative, complementary, or synergistic mechanisms of action. Trial registration:ClinicalTrials.gov identifier: NCT02257177. Trial registration:ClinicalTrials.gov identifier: NCT02738801. Trial registration:ClinicalTrials.gov identifier: NCT02538536. Trial registration:ClinicalTrials.gov identifier: NCT02503657. Trial registration:ClinicalTrials.gov identifier: NCT01371305. Trial registration:ClinicalTrials.gov identifier: NCT02550873. Trial registration:ClinicalTrials.gov identifier: NCT02688647. Trial registration:ClinicalTrials.gov identifier: NCT01872689. Trial registration:ClinicalTrials.gov identifier: NCT01529853. Trial registration:ClinicalTrials.gov identifier: NCT02345070. Trial registration:ClinicalTrials.gov identifier: NCT01629667. Trial registration:ClinicalTrials.gov identifier: NCT01890265. Trial registration:ClinicalTrials.gov identifier: NCT01262001. Trial registration:ClinicalTrials.gov identifier: NCT03142191. Trial registration:ClinicalTrials.gov identifier: NCT02036970. Trial registration:ClinicalTrials.gov identifier: NCT00463983. Trial registration:Japan Primary Registries Network identifier: JapicCTI-183898.
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U2 - 10.1080/13543784.2019.1554054
DO - 10.1080/13543784.2019.1554054
M3 - Article
C2 - 30513000
AN - SCOPUS:85058146463
VL - 28
SP - 19
EP - 28
JO - Expert Opinion on Investigational Drugs
JF - Expert Opinion on Investigational Drugs
SN - 1354-3784
IS - 1
ER -