Trial · NCT07896252
Phase 2b Efficacy and Safety Study of AERO-007, an Inhaled LABA+LAMA Combination for Nebulization Delivery in COPD Patients
NCT07896252, Phase 2, Recruiting, AeroRx Therapeutics Inc.
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Phase 2b Efficacy and Safety Study of AERO-007, an Inhaled LABA+LAMA Combination for Nebulization Delivery in COPD Patients. Trials, record NCT07896252. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896252
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Phase 2b Efficacy and Safety Study of AERO-007, an Inhaled LABA+LAMA Combination for Nebulization Delivery in COPD Patients
- NCT number
- NCT07896252
- Status
- Recruiting
- Phases
- Phase 2
- Enrollment
- 64 participants, estimated
- Lead sponsor
- AeroRx Therapeutics Inc.
- Conditions
- COPD, Chronic Obstructive Pulmonary Disease (COPD), Lung Disease Chronic, Lung Diseases, Obstructive
- Interventions
- AERO-001, AERO-002, AERO-007
- First posted
- 2026-10-26
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Bronchodilation - FEV1 | Change from baseline in FEV1 at 24 hours post-dose on Days 1 and 14 | |
| Primary | Bronchodilation - FEV AUC | Change from baseline in FEV1 AUC(0-24 hours) on Days 1 and 14 | |
| Primary | Bronchodilation - Peak FEV1 | Peak change in FEV1 within 4 hours post-dose on Days 1 and 14 | |
| Primary | Bronchodilation - time to onset of FEV1 >100mL | Change in FEV1 >100mL from pre-dose on Days 1 and 14 | |
| Secondary | Pharmacokinetics - Cmax | 0-24 hours on Days 1 and 14 | Cmax (maximum plasma concentration) |
| Secondary | Pharmacokinetics - AUC | AUC(0-6 hours) on Days 1 and 14 | AUC (area under the plasma concentration) |
| Secondary | Pharmacokinetics - Tmax | Tmax on Days 1 and 14 | Tmax (time to maximum concentration) |
| Secondary | Treatment-emergent adverse events (TEAEs) | Up to approximately Day 14 | Number of participants with TEAEs |
| Secondary | Blood Pressure | Up to approximately Day 14 | Number of participants with markedly abnormal changes in Blood Pressure |
| Secondary | Heart Rate | Up to approximately Day 14 | Number of participants with markedly abnormal changes in Heart Rate |
1 to 10 of 13Source ClinicalTrials.gov
See all 13 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07896252
GET https://conductscience.org/api/trials/v1/NCT07896252/registered