Sustained Release Oral Formulation For Treatment Of Parkinsons Disease

University of Minnesota

Source: ClinicalTrials.gov (U.S. National Library of Medicine), data processed 2026-10-29T09:00:05; modifications: selected fields only; whitespace normalized; brief summary truncated to 2,000 characters. Not a U.S. Government endorsement.

Brief summary

LD/CD (medications to treat Parkinson's disease) will be delivered using an assembly of nested sachets made of permeable material. The assembly is placed in the oral/buccal cavity (between cheek and gum of lower jaw) and delivers continuous release of CD and LD for both transmucosal and gastrointestinal absorption. The combination of CD/LD in the inner sachet varies from that in the outer sachet. This allows for sequential release of CD and then LD to mimic a CD pretreatment method which is known to increase LD absorption and prolong its half-life.

Source: ClinicalTrials.gov (U.S. National Library of Medicine), data processed 2026-10-29T09:00:05; modifications: selected fields only; whitespace normalized; brief summary truncated to 2,000 characters. Not a U.S. Government endorsement.

Trial details

status
NOT_YET_RECRUITING
phase
PHASE1, PHASE2
study type
INTERVENTIONAL
enrollment
32
sponsor
University of Minnesota
conditions
Healthy Volunteers
interventions
DRUG: Formulation A; DRUG: Formulation B; DRUG: Formulation C
start date
2027-04-01
start date type
ESTIMATED
primary completion date
2027-06-30
has results
false
data source
ClinicalTrials.gov
data processed
2026-10-29T09:00:05
modifications
selected fields only; whitespace normalized; brief summary truncated to 2,000 characters

Record

Archive ID
nct:NCT07709741
Published
Jul 16, 2026
Updated
Oct 1, 2026
Venue
ClinicalTrials.gov
ClinicalTrials.gov
NCT07709741
Categories
Healthy Volunteers
License
ClinicalTrials.gov terms (attribution, processing date, modifications noted)
Provenance
clinicaltrials

Topics