Biopharma Transcript

Liquidia Corp LQDA

Nasdaq · Phase 3 · respiratory · device-combination · EDGAR · Updated Nov 2, 2026

Liquidia Corp (Nasdaq: LQDA) is a respiratory drug developer. Its lead program, L606 (liposomal treprostinil, inhaled via next-generation nebulizer), is in Phase 3 for pulmonary hypertension associated with interstitial lung disease (PH-ILD); also PAH (open-label).

Upcoming catalysts

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

Pipeline

ProgramIndicationModalityStage
YUTREPIA (treprostinil inhalation powder)PAH and PH-ILD (approved May 2025); planned studies in PH-COPD, IPF, PPF, SSc-RPdevice-combinationApproved
L606 pivotal studyPH-ILDdevice-combinationPhase 3
L606 open-label study (US)PAH and PH-ILDdevice-combinationPhase 2
YUTREPIA new-indication studiesPH-COPD, IPF, PPF, SSc-RPdevice-combinationPre-clinical

Recent results and decisions

  1. Oct 14, 2026
    n/a Liquidia will continue studies to explore YUTREPIA for systemic sclerosis-associated Raynaud's phenomenon (SSc-RP) where no approved options exist.We will continue to build on our market position through new studies to explore novel treatments for conditions like systemic sclerosis-associated Raynaud's phenomenon (SSc-RP). Filing
  2. Oct 14, 2026
    n/a Liquidia will continue pivotal studies of L606 to support PAH indication.We will continue to build on our market position through pivotal studies of L606 to support PAH and PH-ILD indications. Filing
  3. Oct 14, 2026
    n/a Liquidia continues pivotal studies of L606 to support PAH indication.And simultaneously, we will continue to build on our market position through post-marketing studies of YUTREPIA, pivotal studies of L606 to support PAH and PH-ILD indications, and new studies to explore novel treatments for conditions like systemic sclerosis-associated Raynaud's phenomenon (SSc-RP) Filing

7 more on record.

For subscribers

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