A study to compare the absorption of two tablet strengths with the absorption of a solution.

2024-519835-41-00 Protocol ARV-102-104 Human pharmacology (Phase I) - Bioequivalence study Ended

Start 28 Feb 2025 · End 25 Jun 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol ARV-102-104

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Bioequivalence study
Status Ended
Participants planned 18
Countries 1
Sites 1

Parkinson's Disease

Key facts

Sponsor
Arvinas Operations Inc.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Phenomena and Processes [G] - Musculoskeletal and Neural Physiological Phenomena [G11]
Trial duration
28 Feb 2025 → 25 Jun 2025
Decision date (initial)
2025-02-27
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Parkinson's Disease

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Arvinas Operations Inc.

Sponsor organisation
Arvinas Operations Inc.
Address
5 Science Park
City
New Haven
Postcode
06511-1966
Country
United States

Scientific contact point

Organisation
Arvinas Operations Inc.
Contact name
Clinical Trials NS

Public contact point

Organisation
Arvinas Operations Inc.
Contact name
Clinical Trials NS

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Ended 18 1
Rest of world 0

Investigational sites

Netherlands

1 site · Ended
Centre for Human Drug Research
Neurology, Zernikedreef 8, 2333 CL, Leiden

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Netherlands 2025-02-28 2025-06-25 2025-03-10 2025-06-25

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-01-21 Netherlands Acceptable
2025-02-27
2025-02-27
2 SUBSTANTIAL MODIFICATION SM-1 2025-03-31 Netherlands Acceptable
2025-04-09
2025-04-09