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  2. Nintedanib - Wikipedia

    en.wikipedia.org/wiki/Nintedanib

    Nintedanib is used for the treatment of idiopathic pulmonary fibrosis. [9] It has been shown to slow down decrease in forced vital capacity, [10] [11] and it also improves people's quality of life. [12] Nintedanib does not improve survival in people with IPF. [13]

  3. Idiopathic pulmonary fibrosis - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_pulmonary_fibrosis

    Idiopathic pulmonary fibrosis; Other names: Fibrosing alveolitis, cryptogenic fibrosing alveolitis, diffuse fibrosing alveolitis, usual interstitial pneumonitis, diffuse interstitial pneumonitis: Figure A shows the location of the lungs and airways in the body. The inset image shows a detailed view of the lung's airways and air sacs in cross ...

  4. Pulmonary fibrosis - Wikipedia

    en.wikipedia.org/wiki/Pulmonary_fibrosis

    The actual number may be significantly higher due to misdiagnosis. Typically, patients are in their forties and fifties when diagnosed, while the incidence of idiopathic pulmonary fibrosis increases dramatically after age 50. But loss of pulmonary function is commonly ascribed to old age, heart disease, or more common lung diseases. [40]

  5. List of dog diseases - Wikipedia

    en.wikipedia.org/wiki/List_of_dog_diseases

    Dogs are ten times more likely to be infected than humans. The disease in dogs can affect the eyes, brain, lungs, skin, or bones. [15] Histoplasmosis* is a fungal disease caused by Histoplasma capsulatum that affects both dogs and humans. The disease in dogs usually affects the lungs and small intestine. [16]

  6. Report: PIF’s LIV Golf investment nearing $5B as losses mount

    www.aol.com/report-pif-liv-golf-investment...

    The Saudi Arabia Public Investment Fund is nearing $5 billion in total investment in LIV Golf, according to financial documents reviewed by the Money in Sport newsletter on Thursday.

  7. Ziritaxestat - Wikipedia

    en.wikipedia.org/wiki/Ziritaxestat

    Ziritaxestat is a small-molecule, selective autotaxin inhibitor that was investigated as a potential treatment for idiopathic pulmonary fibrosis (IPF). [1] Initially showing promise in early-phase studies, ziritaxestat underwent evaluation in two large-scale phase 3 clinical trials, ISABELA 1 and ISABELA 2.

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