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. 2020 Feb;62(2):178–190. doi: 10.1165/rcmb.2018-0147OC

Table 1.

Interactions with P-gp and BCRP for Approved and Study Drugs for Idiopathic Pulmonary Fibrosis*

Status Drug P-gp BCRP
Approved      
  Pirfenidone Inhibitor
  Nintedanib Substrate
Phase 3      
  Ambrisentan Substrate
  Bosentan Substrate
  Warfarin Inhibitor, substrate
  Imatinib Substrate Substrate
  Sildenafil Inhibitor
  IFN-γ Inducer
  Trimethoprim§ Inhibitor, inducer
  NAC
Phase 2      
  Losartan Substrate, inhibitor
  Prednisone Substrate, inhibitor
  Macitentan Inducer
  BG00011 (STX100)
  PRM-151
  SAR156597
  TD139
  Treprostinil
  GLPG1690
  Tetrathiomolybdate
  Zileuton
  Etanercept
  BMS-986020
  KD025
  CC-90001
  Compound 36 (GBT440)
  PBI-4050
  Tipelukast
  Octreotide
  Azathioprine
  QAX576
Phase 1      
  Dasatanib Substrate, inhibitor
  Vismodegib§ Substrate Inhibitor
  Sirolimus Inhibitor, inducer
  Quercetin§ Inhibitor Inhibitor
  IW001
  Nandrolone decanoate
  Omipalisib (GSK2126458)
  GSK3008348
  Tanzisertib (CC-930)
Preclinical      
  Colchicine Substrate, inhibitor, inducer
  Felodipine Inhibitor
  Atorvastatin Inhibitor
  Protectin DX
  Everolimus

Definition of abbreviations: BCRP = breast cancer resistance protein; NAC = N-acetylcysteine; P-gp = permeability glycoprotein.

*

This table was compiled using DrugBank 5.0 (www.drugbank.ca), which is a comprehensive drug database supported by the Canadian Institutes of Health Research (40). This is not a list of all drugs in development as therapy for idiopathic pulmonary fibrosis.

Negative results.

Currently recruiting participants (www.clinicaltrials.gov).

§

In a combination strategy.