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Pulmatrix Announces Year-End and Q4 Financial 2022 Results and Provides Corporate Update

PUR1900 Phase 2b study dosed first patients in Q1 2023 PUR3100 Phase 1 study achieves positive topline results as announced in Q1 2023 $35.6 million in cash

articlePulmatrix, Inc.March 30, 20234/company/pulmatrix-inc/news/pulmatrix-announces-year-end-and-q4-financial-2022-results-and-provides-corporate-update
Pulmatrix Announces Year-End and Q4 Financial 2022 Results and Provides Corporate Update

About this update from Pulmatrix, Inc.

[{"type":"text","content":"PUR1900 Phase 2b study dosed first patients in Q1 2023\nPUR3100 Phase 1 study achieves positive topline results as announced in Q1 2023\n$35.6 million in cash and cash equivalents at the end of 2022 providing cash runway into Q2 2024\nLEXINGTON, Mass., March 30, 2023 /PRNewswire/ -- Pulmatrix, Inc. (NASDAQ: PULM), a clinical-stage biopharmaceutical company developing innovative inhaled therapies to address serious pulmonary and central nervous system disease using its patented iSPERSE™ technology, today announced fourth quarter and year-end financial results for 2022 and provided a corporate update on its development programs.\n\n \n \n \n \n \n \n\n \nTed Raad, Chief Executive Officer of Pulmatrix commented, \"2022 was a year of significant progress for all of our development programs, setting the stage for significant milestone accomplishments in 2023. In 2022, we completed the Phase 1b study of PUR1800 for acute exacerbations in chronic obstructive pulmonary disease (AECOPD), for which the data was presented this year. We also initiated and completed a Phase 1 study of PUR3100, our orally inhaled formulation of dihydroergotamine (DHE) for acute migraine, allowing us to begin 2023 by announcing data that we believe illustrates a potentially positive pharmacokinetic and pharmacodynamic profile for PUR3100 – including a rapid systemic exposure within the targeted therapeutic range, and fewer side effects compared to intravenous (IV) dosing. Finally, we prepared for a Phase 2b study of PUR1900 in allergic bronchopulmonary aspergillosis (ABPA) and announced the first patient dosed in Q1 2023. We are grateful for the potential opportunity to positively impact patients with these programs and are proud of the Company's accomplishments throughout last year and into this year.\"\n2022 and Recent Program and Corporate Highlights\nPUR1900\nIn February 2023, Pulmatrix began dosing patients for its Phase 2b study of PUR1900. This Phase 2b trial is designed as a randomized, double-blind, multi-center, placebo-controlled study to evaluate the efficacy and duration of treatment with itraconazole, administered as a dry powder for inhalation (PUR1900). The goal of the study is to provide data on potential registrational endpoints in ABPA in patients with asthma. The multi-center study is being conducted in the United States, United Kingdom, Au...

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