The purpose of this study is to evaluate the long-term safety and tolerability of Admilparant in participants who completed participation in parent studies IM027-068 (for idiopathic pulmonary fibrosis (IPF)) and IM027-1015 (for progressive pulmonary fibrosis (PPF)).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
2,277
Specified dose on specified days
Number of Participants With Treatment Emergent Adverse Events (TEAEs)
Time frame: Up to Week 100
Number of Participants With Serious Adverse Events (SAEs)
Time frame: Up to Week 100
Number of Participants With AEs leading to Discontinuation
Time frame: Up to Week 100
Number of Participants With AEs leading to Deaths
Time frame: Up to Week 100
Number of Participants With Clinically Significant Laboraty Abnormalities
Time frame: Up to Week 100
Number of Participants With Clinically Significant Electocardiogram (ECG) Abnormalities
Time frame: Up to Week 100
Number of Participants With Clinically Significant Vital Sign Abnormalities
Time frame: Up to Week 100
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Local Institution - 0013
Florida, Vicente López, Buenos Aires, Argentina
Local Institution - 0014
Mar del Plata, Buenos Aires, Argentina
Local Institution - 0007
Quilmes, Buenos Aires, Argentina
Local Institution - 0009
San Juan Bautista, Buenos Aires, Argentina
Local Institution - 0003
Mar del Plata, B, Argentina
Local Institution - 0001
Córdoba, Córdoba Province, Argentina
Local Institution - 0005
CABA, Distrito Federal, Argentina
Local Institution - 0002
Godoy Cruz, Mendoza Province, Argentina
Local Institution - 0011
Mendoza, M, Argentina
Local Institution - 0015
Rosario, S, Argentina
...and 152 more locations