deltatrials
Completed PHASE2 INTERVENTIONAL 2-arm NCT05262218

Therapeutic Effect of PBF-680 in Patients With COPD (Respire)

A Phase IIa, Randomized, Double Blind, Placebo Controlled Study to Assess the Effect of PBF-680 in Patients With Moderate to Severe COPD on Top of the Standard Medication

Sponsor: Palobiofarma SL

Conditions COPD
Updated 6 times since 2022 Last updated: Apr 18, 2024 Started: Dec 20, 2021 Primary completion: Feb 27, 2024 Completion: Apr 9, 2024
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT05262218, this PHASE2 trial focuses on COPD and remains completed. Sponsored by Palobiofarma SL, it has been updated 6 times since 2021, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.

Status Flow

~Apr 2022 – ~Feb 2023 · 10 months · monthly snapshotRecruiting~Feb 2023 – ~Mar 2024 · 13 months · monthly snapshotRecruiting~Mar 2024 – ~May 2024 · 2 months · monthly snapshot~May 2024 – ~Jul 2024 · 2 months · monthly snapshot~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshot~Sep 2024 – present · 23 months · monthly snapshotCompleted

Change History

6 versions recorded
  1. Sep 2024 — Present [monthly]

    Completed PHASE2

  2. Jul 2024 — Sep 2024 [monthly]

    Completed PHASE2

  3. May 2024 — Jul 2024 [monthly]

    Completed PHASE2

    Status: Active Not RecruitingCompleted

  4. Mar 2024 — May 2024 [monthly]

    Active Not Recruiting PHASE2

    Status: RecruitingActive Not Recruiting

  5. Feb 2023 — Mar 2024 [monthly]

    Recruiting PHASE2

Show 1 earlier version
  1. Apr 2022 — Feb 2023 [monthly]

    Recruiting PHASE2

    First recorded

Dec 2021

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Palobiofarma SL
  • Scope International AG
Data source: Palobiofarma SL

For direct contact, visit the study record on ClinicalTrials.gov .