A Study to Test the Safety and Effects of Inhaled GDC-6988 in Participants With Muco-obstructive Disease
NCT06603246 · Status: RECRUITING · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 128
Last updated 2026-05-05
Summary
This study evaluates the safety, tolerability, and activity of inhaled GDC-6988 in participants with muco-obstructive disease.
Conditions
- Non-cystic Fibrosis Bronchiectasis
- Chronic Obstructive Pulmonary Disease
Interventions
- DRUG
-
GDC-6988
GDC-6988 will be administered using a dry powder inhalation (DPI) device.
Sponsors & Collaborators
-
Genentech, Inc.
lead INDUSTRY
Principal Investigators
-
Clinical Trials · Genentech, Inc.
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-11-18
- Primary Completion
- 2027-11-15
- Completion
- 2027-11-15
- FDA Drug
- Yes
Countries
- United States
Study Locations
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