Alpha-1 MP
BiologicalOther names: Prolastin-C
NCT Number: NCT01983241
This is a multi-center, randomized, placebo-controlled, double blind clinical study to assess the efficacy and safety of two separate dose regimens of Alpha-1 MP versus placebo for 156 weeks (i.e., 3 years) using computed tomography (CT) of the lungs as the main measure of efficacy. The two Alpha-1 MP doses to be tested are 60 mg/kg and 120 mg/kg administered weekly by IV infusion for 156 weeks. The study consists of an optional pre-screening phase, Screening Phase, a 156-week Treatment Phase, and an End of Study Visit at Week 160.
This study is active but is not currently recruiting participants.
Notify Me18 year–70 year
All sexes
Interventional
Phase 3
Grifols Investigative Site, Vicente López, Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: Prolastin-C
Other names: Saline
Time frame: Week -3 (baseline measure), Week 52, Week 104, Week 130, Week 156
Whole lung PD15 measured by CT scan
Time frame: Week -3 through Week 160
Monitoring of AEs
Time frame: Week -3 through Week 160
Monitoring of SAEs
Time frame: Week -3 through Week 160
Monitoring of discontinuations due to AEs
Time frame: Week -3 through Week 160
Severe COPD exacerbations as defined by American Thoracic Society/European Respiratory Society (ATS/ERS) criteria (i.e., COPD exacerbations requiring hospitalization)
Time frame: Week -3 (baseline measure), Week 52, Week 104, Week 130, Week 156
PD15 of the basal lung region measure by CT scan
Time frame: Weeks 26, 52, 78, 104, 130 and 156
DLco performed according to American Thoracic Society/European Respiratory Society (ATS/ERS) guidelines
Time frame: Weeks 26, 52, 78, 104, 130 and 156
FEV1 performed according to ATS/ERS guidelines
Time frame: Weeks 26, 52, 78, 104, 130 and 156
Health-related quality of life assessment tool
Time frame: Weeks 26, 52, 78, 104, 130 and 156
Heath-related quality of life assessment tool
Grifols Therapeutics LLC
Industry
A Randomized, Double-Blind, Placebo Controlled Study to Assess the Efficacy and Safety of Two Dose Regimens (60 mg/kg and 120 mg/kg) of Weekly Intravenous Alpha1 Proteinase Inhibitor (Human) in Subjects With Pulmonary Emphysema Due to Alpha1 Antitrypsin Deficiency
Acronym: SPARTA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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