Michael Schweitzer Barrios
CLIN AST PROF
JX-MEDICINE AT JAX
GRANTS
- GRANTA Phase 2b/Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study, to Investigate the Efficacy and Safety of Lunsekimig In Adult Participants with Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD) Characterized by an Eosinophilic PhenotypeSanofi Us Services9 Jun 2026 - 8 Jun 2031
- GRANTA Phase IIb Randomized, Double-blind, Placebo-controlled, Parallel, Multidose Study to Evaluate the Efficacy, Safety, and PK of AZD0292 in Participants 12 years of age and older with Bronchiectasis and Chronic Pseudomonas aeruginosa Colonization (CLEAR)Astrazeneca Pharm5 Sep 2025 - 4 Sep 2030
- GRANTA Phase III, randomised, double-blind, placebo-controlled study to assess the efficacy, safety, and tolerability of BI 1291583 2.5 mg administered once daily for up to 76 weeks in patients with bronchiectasis (The AIRTIVITY® Study)Boehringer Ingelheim International Gmbh27 May 2025 - 26 May 2030
- GRANTA Randomised, Double-blind, Placebo-controlled, Parallel Group, Multicentre, Phase 3 Study to Evaluate the Efficacy and Safety of Tezepelumab in Adult Participants with Moderate to Very Severe Chronic Obstructive Pulmonary DiseaseAstrazeneca Pharm3 Apr 2025 - 3 Apr 2030
- GRANTA Phase 2/3 Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Investigate the Safety and Efficacy of Oral Brepocitinib in Adults with Cutaneous SarcoidosisPriovant Therapeutics14 Mar 2025 - 14 Mar 2030
- GRANTICoN-1: A Randomized, Double-Blind, Placebo-Controlled Phase 3 Study of the Efficacy and Safety of Treatment With MNKD-101 (Clofazimine Inhalation Suspension) When Added to Guideline-Based Therapy in Participants with Pulmonary Nontuberculous Mycobacterial Infection (Part A) Followed by an Open-Label Extension (Part B)Mannkind26 Sep 2024 - 20 Aug 2026
- GRANTmyAirvo 3 (High Flow Nasal Therapy) for COPD patients in the home – a multi-center randomized controlled trialFisher & Paykel Healthcare5 Jan 2024 - 31 Dec 2027
- GRANTA randomised, double-blind, parallel group, roll-over study evaluating long-term safety and efficacy of oral doses of BI 1291583 q.d. (Part A) followed by open label long-term safety assessment (Part B) in patients with bronchiectasis (ClairleafTM)Boehringer Ingelheim International Gmbh28 Oct 2020 - 29 Sep 2028