Drug class

Pulmonary Fibrosis Treatment Agents - Antifibrotic Therapy

The phrase "Pulmonary Fibrosis Treatment Agents - Antifibrotic Therapy" is a commercial formulary compendium category—specifically applied to pirfenidone—rather than a formal FDA-established pharmacologic class. Read more about Pulmonary Fibrosis Treatment Agents - Antifibrotic Therapy

34 drugs in this class 27 manufacturers

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Drugs in Pulmonary Fibrosis Treatment Agents - Antifibrotic Therapy

Showing 28–34 of 34 drugs

NINTEDANIB ESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · SYSTEMIC SCLEROSIS-ASSOCIATED INTERSTITIAL LUNG DISEASE ·+2
GSMS, INC.

NINTEDANIB ESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · SYSTEMIC SCLEROSIS-ASSOCIATED INTERSTITIAL LUNG DISEASE ·+2
EXELAN PHARMACE

NINTEDANIB ESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · SYSTEMIC SCLEROSIS-ASSOCIATED INTERSTITIAL LUNG DISEASE ·+2
GLENMARK PHARMA

NINTEDANIB ESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · SYSTEMIC SCLEROSIS-ASSOCIATED INTERSTITIAL LUNG DISEASE ·+2
AVKARE

NINTEDANIB ESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · SYSTEMIC SCLEROSIS-ASSOCIATED INTERSTITIAL LUNG DISEASE ·+2
MACLEODS PHARMA

NINTEDANIB ESYLATE

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS · SYSTEMIC SCLEROSIS-ASSOCIATED INTERSTITIAL LUNG DISEASE ·+2
SANDOZ

PIRFENIDONE

PULMONARY FIBROSIS TREATMENT AGENTS - ANTIFIBROTIC THERAPY · IDIOPATHIC PULMONARY FIBROSIS
MACLEODS PHARMA
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About Pulmonary Fibrosis Treatment Agents - Antifibrotic Therapy.

The phrase "Pulmonary Fibrosis Treatment Agents - Antifibrotic Therapy" is a commercial formulary compendium category—specifically applied to pirfenidone—rather than a formal FDA-established pharmacologic class.

Clinically, these agents exert antifibrotic, anti-inflammatory, and antioxidant properties by downregulating pro-fibrotic growth factors and cytokines, notably transforming growth factor-beta (TGF-beta), thereby inhibiting fibroblast proliferation and collagen synthesis.

Their primary therapeutic role is to slow the decline of lung function and reduce disease progression in adults with idiopathic pulmonary fibrosis (IPF) and related progressive fibrosing interstitial lung diseases.