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NCT06175065Active, not recruitingPhase 2

Safety, PK and PD Relationships of RLS-0071 in Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease

A Phase 2a Randomized, Doubled-Blind, Placebo-Controlled Trial to Evaluate Safety, Pharmacokinetics and Pharmacokinetic-Pharmacodynamic Relationships of RLS-0071 in Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Source: ClinicalTrials.gov · Last updated 8 May 2025

Brief summary (registry, in English)

AECOPD is a major cause of hospital admission and mortality. They contribute to long-term decline in lung function, physical capacity, and quality of life (QoL). RLS-0071 is a novel peptide being developed for the treatment of AECOPD. This study is designed to evaluate the safety and tolerability of RLS-0071 in the treatment of adults with moderate exacerbations of COPD.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
24 (estimated)
First submitted
29 Nov 2023
Start date
25 Jan 2024
Primary completion date
Jun 2025
Lead sponsor
ReAlta Life Sciences, Inc.
Diseases
COPD
NCT number
NCT06175065

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 24
  • From 25 Jan 2024 to the primary completion date, Jun 2025
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current or prior history of asthma.
  • Preexisting autoimmune disease: History of autoimmune disease and/or use of chronic steroids of \>10mg/d (prednisone or equivalent) for more than 14 days prior to enrollment
  • Has confounding medical conditions, including:
    • diabetic coma,
    • uncontrolled New York Heart Association Class IV congestive heart failure,
    • uncontrolled angina,
    • stroke or transient ischemic attack (TIA) within 4 weeks before study entry,
    • clinically significant arrhythmias not controlled by medication, or
    • idiopathic pulmonary fibrosis,

Other illness

  • Interstitial lung disease.
  • Known hypersensitivity, allergy, or reaction to polyethylene glycol (PEG)

Other

  • Endotracheal intubation or mechanical ventilation.
  • Participants with severe exacerbation of COPD according to the Rome guidelines
  • Participants with signs and symptoms consistent with an alternative diagnosis for worsening of pulmonary status
  • Current renal dialysis or renal dialysis planned or anticipated in the next 7 days.
  • Has a weight \>120 kg at Screening.
  • Known pregnancy, a positive pregnancy test at screening, or lactation for WOCBP.
  • Has systemic immunosuppression/immune deficiency

Who the study is looking for

  • Hospitalized participants with a prior diagnosis of COPD including spirometry within the prior year documenting a postbronchodilator FEV1/FVC ≤ 0.7 and an FEV1
    • ≤ 80%, and a clinician identified admitting diagnosis of AECOPD: acute increase in dyspnea, sputum volume or purulence - without other attributable cause.
  • Participants must have a moderate exacerbation of COPD according to the Rome guidelines
  • ≥ 10 pack-years smoking history.

Age in the registry: 30 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
Glen BurnieUnited StatesUnknown status
-
Coordinator of this site? Confirm its status
OmahaUnited StatesUnknown status
-
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
-
Coordinator of this site? Confirm its status
St. PetersburgUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.