Bioequivalence study 2 to compare pharmacokinetics of Parkinson´s disease drugs in healthy volunteers

2026-525449-57-00 Protocol 3135003 Human pharmacology (Phase I) - Bioequivalence study Ended

Start 8 Apr 2026 · End 13 May 2026 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol 3135003

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Bioequivalence study
Status Ended
Participants planned 40
Countries 1
Sites 1

Parkinson desease

Key facts

Sponsor
Orion Corporation
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Nervous System Diseases [C10]
Trial duration
8 Apr 2026 → 13 May 2026
Decision date (initial)
2026-03-27
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
Yes

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Parkinson desease

VersionLevelCodeTermSystem organ class
20.0 PT 10061536 Parkinson's disease 100000004852

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Orion Corporation

Sponsor organisation
Orion Corporation
Address
P. O. Box 65
City
Espoo
Postcode
02101
Country
Finland

Scientific contact point

Organisation
Orion Corporation
Contact name
clinical department

Public contact point

Organisation
Orion Corporation
Contact name
clinical department

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Czechia Ended 40 1
Rest of world 0

Investigational sites

Czechia

1 site · Ended
Cepha s.r.o.
clinic, Komenskeho 19, Severni Predmesti, Plzen

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Country Trial startTrial end Recruitment startRecruitment end Early termination
Czechia 2026-04-08 2026-05-13 2026-04-08 2026-04-17

Application history

1 submissions — initial application plus substantial / non-substantial modifications

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2026-03-03 Czechia Acceptable
2026-03-27
2026-03-27