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Randomized Controlled Trial
. 2019 Jul;16(7):927-930.
doi: 10.1513/AnnalsATS.201810-720RL.

Pirfenidone Treatment in Individuals with Idiopathic Pulmonary Fibrosis: Impact of Timing of Treatment Initiation

Affiliations
Randomized Controlled Trial

Pirfenidone Treatment in Individuals with Idiopathic Pulmonary Fibrosis: Impact of Timing of Treatment Initiation

Toby M Maher et al. Ann Am Thorac Soc. 2019 Jul.
No abstract available

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Figures

Figure 1.
Figure 1.
Treatment periods for calculating annual forced vital capacity (FVC) decline during CAPACITY and RECAP to assess the association of FVC decline and timing of pirfenidone initiation (aim 2). *Pirfenidone was titrated from 801 mg/d over the first 15 days in RECAP up to the maintenance dose (or maximum tolerated dose if this was lower). CAPACITY = Clinical Studies Assessing Pirfenidone in Idiopathic Pulmonary Fibrosis: Research of Efficacy and Safety Outcomes.
Figure 2.
Figure 2.
Rate of lung function decline over 180 weeks by baseline % predicted forced vital capacity (FVC) category in RECAP.
Figure 3.
Figure 3.
Annual rate of lung function decline in CAPACITY and RECAP by treatment group during CAPACITY. *Annual rates of forced vital capacity (FVC) decline during RECAP were calculated on the basis of all available RECAP FVC values, but only presented up to Week 220. CAPACITY = Clinical Studies Assessing Pirfenidone in Idiopathic Pulmonary Fibrosis: Research of Efficacy and Safety Outcomes. Adapted by permission from Reference .

References

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