Pulmatrix, Inc. (PULM)
Pulmatrix, Inc. (PULM) is a clinical-stage biotechnology firm focused on creating and advancing inhaled treatments. The company's primary goal is to address significant unmet medical needs in respiratory and other diseases within the United States. Central to their approach is the innovative iSPERSE (inhaled small particles easily respirable and emitted) technology. This proprietary platform allows for the precise delivery of both small and large molecule therapeutics directly into the lungs, achieving either localized effects or systemic distribution throughout the body. Pulmatrix's development pipeline includes several key candidates: Pulmazole: An inhaled antifungal drug being developed to treat allergic bronchopulmonary aspergillosis in patients with asthma and cystic fibrosis. PUR1800: A narrow spectrum kinase inhibitor currently undergoing Phase 1b clinical trials for individuals suffering from stable moderate-to-severe chronic obstructive pulmonary disease (COPD). PUR3100: An iSPERSE-formulated version of dihydroergotamine, intended for the rapid relief of acute migraine attacks. The company also maintains strategic collaborations, including a licensing arrangement with RespiVert Ltd. for access to a range of kinase inhibitor drug candidates, a partnership with Cipla Technologies LLC for the development and commercialization of Pulmazole, and a collaboration and license agreement with Sensory Cloud, Inc. Established in 2003, Pulmatrix, Inc. is headquartered in Lexington, Massachusetts.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
Pulmatrix, Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 2Terminated
Study in Adult Asthmatic Patients With Allergic Bronchopulmonary Aspergillosis
PUR1900, Placebo
Allergic Bronchopulmonary Aspergillosis
NCT03960606Enrollment7StartJul 2019Primary CompletionJul 2020CompletionJul 2020 - Phase 2Terminated
Study to Evaluate Itraconazole Administered as Inhaled Dry Powder in Adults With Asthma and ABPA
Itraconazole Powder, Placebo
ABPA
NCT05667662Enrollment8StartFeb 2023Primary CompletionFeb 2024CompletionFeb 2024 - Phase 1/2Terminated
A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60
RUT058-60, Sterile saline for irrigation
Postoperative Wound Infection-deep, Post Operative Wound Infection
NCT02280395Enrollment9StartOct 2014Primary CompletionJun 2015CompletionJun 2015 - Phase 1Completed
Safety and Efficacy Study of Inhaled PUR003 on a Controlled Influenza Virus Challenge in Healthy Adult Subjects
PUR003, Placebo
Healthy
NCT00947687Enrollment24StartJul 2009Primary CompletionSep 2009CompletionOct 2009 - Phase 1Completed
Effect of PUR003 on Asthma
PUR003, Placebo
Asthma, Lung Diseases +1
NCT00989521Enrollment7StartDec 2009Primary CompletionOct 2011CompletionOct 2011 - Phase 1Completed
Safety, Tolerability, and Pharmacodynamic Effect Study of PUR118
PUR118
Chronic Obstructive Pulmonary Disease
NCT01333904Enrollment90StartFeb 2011Primary CompletionJun 2012CompletionJun 2012 - Phase 1Completed
A Safety and Tolerability Study OF PUR118 In Subjects With Cystic Fibrosis
PUR118
Cystic Fibrosis
NCT01543191Enrollment10StartFeb 2012Primary CompletionDec 2012CompletionDec 2012 - Phase 1Completed
Evaluation of the Effect of PUR118 on Ozone Induced Airway Inflammation in Healthy Normal Volunteers
PUR118
Chronic Obstructive Pulmonary Disease (COPD)
NCT01690949Enrollment24StartAug 2012Primary CompletionApr 2013CompletionApr 2013 - Phase 1Completed
A Safety, Pharmacokinetic and Pharmacodynamic Study of PUR0200 in COPD Patients
PUR0200, PUR0200 Placebo
Chronic Obstructive Pulmonary Disease (COPD)
NCT01921712Enrollment38StartJul 2013Primary CompletionDec 2013CompletionDec 2013 - Phase 1Completed
21 Day Cumulative Skin Irritation of RUT058-60
Hypochlorous acid solution 106 mg/L, 0.1% (w/v) Sodium Lauryl Sulfate
Irritation/Irritant
NCT02198963Enrollment43StartJul 2014Primary CompletionAug 2014CompletionSep 2014 - Phase 1Completed
A PK Study to Evaluate PUR0200 and a Reference Product in Healthy Subjects
PUR0200, Reference Product
Healthy
NCT02671825Enrollment42StartJan 2016Primary CompletionMar 2016CompletionMar 2016 - Phase 1Completed
Safety, Tolerability and Pharmacokinetics of PUR1900 (Itraconazole Powder) in Healthy Volunteers and Adults With Asthma
Itraconazole Powder, Itraconazole 200 mg
Asthma
NCT03479411Enrollment58StartFeb 2018Primary CompletionJun 2018CompletionJun 2018 - Phase 1Completed
A Phase 1b Study of PUR1800 in Patients With COPD
Placebo Comparator, PUR1800 250 ug
Chronic Obstructive Pulmonary Disease (COPD)
NCT04759807Enrollment18StartJan 2021Primary CompletionDec 2021CompletionDec 2021 - Phase 1Completed
A Study to Assess the Safety, Tolerability, and Pharmacokinetics of PUR3100 in Health Adults
PUR3100, Dihydroergotamine (D.H.E 45)
Healthy
NCT05351086Enrollment26StartJun 2022Primary CompletionSep 2022CompletionSep 2022 - ObservationalCompleted
Determination of the in Vitro Effects of Cationic Airway Lining Modulators (CALM) on Chronic Obstructive Pulmonary Disease (COPD) Sputum
-
Chronic Obstructive Pulmonary Disease
NCT01096173Enrollment10StartApr 2010Primary CompletionJun 2010CompletionOct 2010
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 2 | Terminated | PUR1900, Placebo | NCT03960606 |
| Phase 2 | Terminated | Itraconazole Powder, Placebo | NCT05667662 |
| Phase 1/2 | Terminated | RUT058-60, Sterile saline for irrigation | NCT02280395 |
| Phase 1 | Completed | PUR003, Placebo | NCT00947687 |
| Phase 1 | Completed | PUR003, Placebo | NCT00989521 |
| Phase 1 | Completed | PUR118 | NCT01333904 |
| Phase 1 | Completed | PUR118 | NCT01543191 |
| Phase 1 | Completed | PUR118 | NCT01690949 |
| Phase 1 | Completed | PUR0200, PUR0200 Placebo | NCT01921712 |
| Phase 1 | Completed | Hypochlorous acid solution 106 mg/L, 0.1% (w/v) Sodium Lauryl Sulfate | NCT02198963 |
| Phase 1 | Completed | PUR0200, Reference Product | NCT02671825 |
| Phase 1 | Completed | Itraconazole Powder, Itraconazole 200 mg | NCT03479411 |
| Phase 1 | Completed | Placebo Comparator, PUR1800 250 ug | NCT04759807 |
| Phase 1 | Completed | PUR3100, Dihydroergotamine (D.H.E 45) | NCT05351086 |
| Observational | Completed | - | NCT01096173 |