Biopharma Transcript

Pulmatrix, Inc. PULM

Nasdaq · Phase 1 · CNS/neurology/psychiatry · small molecule · EDGAR · Updated Oct 24, 2026

Pulmatrix, Inc. (Nasdaq: PULM) is a CNS/neurology/psychiatry drug developer. Its lead program, PUR3100 (inhaled dihydroergotamine, iSPERSE), is in Phase 1 for Acute migraine. Its next catalyst on record is PUR1900: Licensee Cipla expected to commence Phase 3 (ex-US; not sponsored by Pulmatrix) (2026).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: PUR1900 — Licensee Cipla expected to commence Phase 3 (ex-US; not sponsored by Pulmatrix) (2026). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
PUR1900 (inhaled itraconazole)ABPA in asthma / cystic fibrosis (Company's Phase 2b stopped Jan 2024; ex-US development now by licensee Cipla, Phase 3 expected to commence in 2026; Pulmatrix holds 2% ex-US royalty and US rights it seeks to monetize)small moleculePhase 2
PUR3100Acute migraine (Phase 1 complete 2022; Phase 2 IND cleared Sept 2023 but not started; all development on hold pending financing/partner)small moleculePhase 1
PUR1800Acute exacerbations of COPD (Phase 1b complete; development on hold)small moleculePhase 1

Recent results and decisions

  1. Dec 18, 2025
    n/a Pulmatrix and Cullgen mutually waived the no-solicitation clause of their merger agreement to explore alternatives while still awaiting China Securities Regulatory Commission approval.Pulmatrix, Inc. and Cullgen Inc. have mutually agreed to waive the “No Solicitation” clause in the Merger Agreement signed in November 2024 in order to permit each party to explore alternate transactions while continuing to work toward merger approval from the China Securities Regulatory Commission. Filing

For subscribers

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